WEBSITE TERMS OF SERVICE

HyperbaricChamberUSA.com

Legal Entity

Hyperbaric for Life, LLC, doing business as Hyperbaric for Life

Mailing Address

P.O. Box 217, Waddell, Arizona 85355

Telephone

602-737-1160

Effective Date

September 1, 2026

IMPORTANT: These Terms govern use of the Website. They do not replace the labeling, operator manual, installation requirements, written limited warranty, distributor agreement, purchase agreement, or other product-specific documents applicable to a chamber. In any conflict involving safe use, the product labeling and manufacturer-issued safety instructions control.

1. Acceptance of These Terms

These Website Terms of Service (the "Terms") are a binding agreement between you and Hyperbaric for Life, LLC, doing business as Hyperbaric for Life ("Hyperbaric for Life," the "Company," "we," "us," or "our"). They govern your access to and use of HyperbaricChamberUSA.com and any page, content, form, functionality, or service made available through that domain (collectively, the "Website").

By accessing, browsing, submitting information through, or otherwise using the Website, you acknowledge that you have read, understood, and agree to be bound by these Terms and our Privacy Policy. If you access the Website for a business, healthcare facility, distributor, employer, or other organization, you represent that you have authority to bind that organization, and "you" includes both you and that organization. If you do not agree, do not use the Website.

These Terms apply only to the Website unless a provision expressly states otherwise. A product sale, distribution relationship, installation, commissioning, warranty, repair, training engagement, or other commercial transaction is governed by the separately executed documents applicable to that transaction. No Website content creates a sale contract, warranty, service obligation, agency relationship, fiduciary duty, or direct manufacturer-to-end-user relationship.

2. Company Role and Regulatory Description

Hyperbaric for Life is an Arizona medical-device manufacturer and holds a manufacturer permit issued by the Arizona State Board of Pharmacy for activities within the scope of that permit. The Company manufactures hyperbaric chamber models regulated by the U.S. Food and Drug Administration as Class II medical devices under 21 C.F.R. § 868.5470, product code CBF, and lawfully marketed under applicable device-specific FDA 510(k) clearance(s).

FDA 510(k) clearance means that FDA determined the specific cleared device to be substantially equivalent to a legally marketed predicate device for the stated indications for use. Clearance is model-, configuration-, labeling-, and intended-use-specific. It is not a general endorsement of the Company, is not the same as premarket approval, and does not authorize an unlisted model, altered configuration, unapproved claim, off-label promotion, or use contrary to the cleared labeling.

Company chambers are designed and manufactured as pressure vessels for human occupancy. As applicable to the specific chamber, model, serial number, configuration, and data plate, chambers are constructed, inspected, tested, marked, stamped, or certified in accordance with identified provisions of the ASME Boiler and Pressure Vessel Code and ASME PVHO-1, Safety Standard for Pressure Vessels for Human Occupancy. Any statement concerning ASME or PVHO-1 applies only to the particular vessel and components documented as meeting that standard; it is not a blanket certification of a facility, installation, clinical program, operator, or later modification.

A chamber may be appropriate for human treatment only when it is the correct cleared model and configuration, remains within its design and service limits, and is transported, stored, sited, installed, commissioned, maintained, inspected, repaired, and operated in strict accordance with its labeling, data plate, manuals, safety notices, applicable codes, and lawful clinical orders. No pressure vessel or medical device is safe under every condition, and nothing on the Website should be read as an unconditional guarantee of safety.

3. Manufacturer-Distributor Business Model; No Direct Sales

The Company manufactures chambers for and transacts commercially with authorized distributors. The Company does not offer, quote, contract to sell, or sell chambers directly to patients, consumers, facilities, clinicians, or other end users through the Website. Website descriptions, photographs, specifications, requests for information, and references to availability are informational and are not offers capable of acceptance.

All requests concerning pricing, quotations, financing, taxes, delivery, installation, site planning, commissioning, training, warranty registration, routine service, repair scheduling, replacement parts, returns, refunds, cancellation, or other customer support must be directed first to the distributor from which the chamber was purchased or through which the prospective transaction is being handled. Submitting a Website form may permit the Company to identify or refer you to a distributor; it does not create a direct sales or support contract with the Company.

If you do not know the applicable distributor, you may contact the Company at 602-737-1160 and provide the chamber model and serial number. The Company may use that information to identify the distributor of record or appropriate distributor support team. The Company is not obligated to quote, sell, install, service, or support a chamber directly and may refer all routine matters to the distributor.

4. Independent Distributors; No Authority to Bind the Company

Distributors are independent businesses and are not employees, partners, joint venturers, franchisees, fiduciaries, or general agents of the Company. Except for authority expressly granted in a current written distributor agreement, no distributor, salesperson, installer, trainer, consultant, clinician, or other third party may make a promise, representation, warranty, guarantee, waiver, modification, clinical claim, regulatory claim, or commitment on behalf of the Company.

The Company is not responsible for an independent distributor's advertising, pricing, financing, contracting, taxes, sales practices, statements, omissions, recommendations, site evaluation, shipment handling, storage, installation, integration, commissioning, training, maintenance, repair, warranty promises, customer support, or other conduct, except to the extent responsibility cannot lawfully be excluded or the Company expressly assumes the specific responsibility in a writing signed by an authorized Company officer.

A distributor may not alter Company labeling, remove or obscure labels or data plates, modify a chamber, substitute nonapproved components, represent an uncleared use as cleared, expand a Company warranty, or hold itself out as the manufacturer. Any such act is unauthorized unless the Company has expressly approved it in a signed writing and all applicable regulatory requirements have been satisfied.

5. Distributor Responsibilities to Purchasers and End Users

As between the Company and an independent distributor, and subject to the controlling written distributor agreement, the distributor is responsible for the customer-facing sales and support functions it undertakes. These typically include:

accurately identifying the purchaser's requested application, facility type, location, access constraints, and intended operating environment;

providing accurate quotations, commercial terms, payment terms, taxes, delivery terms, return terms, and any distributor-issued warranty or service plan;

communicating product specifications without alteration and without making unauthorized medical, regulatory, performance, reimbursement, or outcome claims;

coordinating site evaluation, delivery, rigging, storage, installation, system integration, commissioning, acceptance testing, documentation, and training through qualified personnel; confirming that the purchaser receives the applicable manuals, labeling, data-plate information, installation requirements, warranty documents, preventive-maintenance schedule, and safety notices; providing first-line customer support, maintaining purchaser and serial-number records, and promptly transmitting safety complaints, suspected device malfunctions, adverse events, and recall communications; performing only work within its authorization, qualifications, and applicable licenses and using only Company-approved parts and procedures; and complying with all laws, codes, permits, professional requirements, and contractual obligations applicable to its sales and services.

This allocation does not excuse any person from duties imposed directly by law and does not transfer to a distributor any nondelegable duty that applicable law places on the Company as manufacturer. It does make clear that the Company does not assume liability for the distributor's independent acts, omissions, promises, or unauthorized services.

6. Product Information; Controlling Documents

The Company attempts to keep Website information accurate and current, but designs, specifications, components, accessories, colors, dimensions, weights, features, standards, software, packaging, and availability may change without Website notice when permitted by law. Photographs and renderings may show optional equipment, earlier configurations, site-specific installations, or items not included with a standard chamber.

Never use Website content as the sole basis for selecting, installing, operating, servicing, modifying, or clinically using a chamber. Before acting, verify the applicable model, serial number, revision, cleared labeling, data plate, approved drawings, installation plan, operator manual, service manual, written safety notices, and current instructions supplied for that specific device. Product-specific documents control over general Website content. If documents appear inconsistent, stop the affected activity and contact the distributor before proceeding.

No Website statement constitutes an engineering drawing, facility plan, code-compliance determination, clinical protocol, medical order, reimbursement representation, or guarantee that a chamber is suitable for a particular building, patient population, indication, workflow, pressure, oxygen-delivery method, or business purpose.

7. No Medical Advice or Provider-Patient Relationship

The Website and all Company-provided general educational materials are for informational purposes only. They do not provide medical advice, diagnosis, treatment, prescribing, credentialing, supervision, or emergency services and do not create a physician-patient, clinician-patient, consultant-client, or other professional relationship.

Hyperbaric oxygen therapy is a medical treatment that must be ordered, supervised, and delivered in accordance with applicable law, the device labeling, professional standards, facility policy, and the judgment of appropriately licensed and credentialed healthcare professionals. Treatment pressure, duration, frequency, oxygen exposure, air breaks, monitoring, contraindications, medication considerations, and patient selection must be determined by qualified professionals. Do not delay or disregard professional medical care because of Website content.

If a patient may be experiencing an emergency, call 911 or the applicable local emergency number. The Website and Company telephone number are not emergency channels and are not continuously monitored for clinical emergencies.

8. Prescription Device; Authorized and Lawful Use

Where a chamber is labeled as a prescription device, federal law restricts sale to or on the order of an appropriately licensed practitioner as stated in the labeling. Each purchaser, facility, distributor, and user is responsible for confirming and complying with prescription, licensure, scope-of-practice, ordering, supervision, documentation, and facility requirements in every jurisdiction where the chamber is sold, installed, or used.

Only trained, qualified, authorized personnel may operate or service a chamber. No patient or untrained person may operate the chamber, alter controls, bypass safety features, or remain without the observation and staffing required by the labeling, facility policy, emergency plan, and applicable standards. Minors and persons unable to understand or follow instructions require safeguards appropriate to their condition and applicable law.

The purchaser and facility must prevent use for an unauthorized purpose, by an unauthorized person, outside the chamber's rated limits, or in a manner inconsistent with the cleared labeling, manuals, warnings, maintenance schedule, or lawful medical order.

9. No Authorization of Off-Label Promotion or Use

Nothing on the Website authorizes a distributor or other person to promote a device for an uncleared indication, make claims inconsistent with the device labeling, or imply that FDA has approved the Company or a clinical outcome. A healthcare professional's independent authority, if any, to use a legally marketed device within professional practice does not authorize the Company, a distributor, or any other seller to market the device unlawfully or to disregard labeling and safety requirements.

The Company disclaims responsibility for claims, protocols, advertisements, social-media posts, handouts, consent forms, reimbursement materials, or other content created by distributors, facilities, clinicians, consultants, or other third parties unless the Company expressly approved the exact content in a signed writing.

10. Purchaser and Facility Due Diligence

Before contracting with a distributor or accepting delivery, the purchaser and facility are responsible for conducting appropriate clinical, legal, engineering, architectural, financial, insurance, and operational due diligence. This includes determining whether the selected model and configuration are lawful and suitable for the intended site and use; identifying the authority having jurisdiction; securing necessary approvals; and budgeting for infrastructure, staffing, oxygen, maintenance, inspections, training, emergency preparedness, and ongoing compliance.

No Website content or distributor referral is a representation that zoning, building, fire, electrical, mechanical, plumbing, medical-gas, healthcare-facility, occupational-safety, accessibility, accreditation, reimbursement, or professional requirements have been satisfied. Requirements differ by location and may change.

11. Site Planning, Utilities, and Facility Compliance

The facility owner and operator, together with their licensed design professionals, contractors, medical-gas professionals, fire officials, and other qualified personnel, are solely responsible for site readiness and facility compliance unless a signed agreement expressly assigns a specific task to the Company. Responsibilities include structural capacity; access and rigging; anchoring; egress; room size; environmental conditions; ventilation; grounding and bonding; electrical service; compressed-air quality and capacity; medical-gas supply and distribution; oxygen exhaust routing; fire detection and suppression; communications; lighting; equipment clearances; drainage; security; and all permits and inspections.

The facility must comply with the version of NFPA 99 and other codes adopted by the authority having jurisdiction, as well as all applicable federal, state, local, accreditation, and insurer requirements. References to NFPA, ASME, PVHO-1, or other standards on the Website do not constitute a facility certification, code opinion, engineering approval, or representation that the authority having jurisdiction will approve a particular site.

The purchaser must provide complete and accurate site information. The Company is not liable for delay, cost, damage, noncompliance, or inability to install arising from concealed conditions, inaccurate measurements, inadequate access, insufficient utilities, deficient construction, unapproved plans, code changes, or site work performed by others.

12. Shipping, Delivery, Rigging, and Storage

Shipping, delivery, risk of loss, title, insurance, inspection, claims deadlines, and acceptance are governed by the applicable written sale documents between the purchaser and distributor and, separately, between the distributor and Company. Website content does not alter those terms.

The distributor, carrier, rigger, warehouse, purchaser, and facility are responsible for handling, lifting, transporting, protecting, and storing the chamber in accordance with Company instructions and accepted professional practices. The chamber must not be dropped, impacted, exposed to prohibited temperatures, humidity, ultraviolet light, direct heat, corrosive substances, contamination, or other conditions that can damage the vessel, acrylic, seals, controls, piping, coatings, or safety systems.

Visible or suspected shipping damage must be documented and reported immediately under the applicable freight and purchase procedures. A damaged or potentially damaged chamber must not be installed or operated until it has been evaluated and released by qualified authorized personnel. The Company is not liable for damage caused after custody transfers from the Company, except to the extent a signed agreement or applicable law provides otherwise.

13. Installation and Commissioning

A chamber may be installed, connected, integrated, tested, and commissioned only by persons qualified for the work and authorized as required by the Company, applicable law, and the authority having jurisdiction. Installation must follow the approved drawings, manuals, labeling, specifications, and site-specific plan. Successful factory testing does not substitute for proper site installation and commissioning.

Unless the Company expressly assumes a defined installation task in a signed agreement, the distributor and its selected installers are responsible for installation and commissioning. The Company has no liability for incorrect, incomplete, delayed, unauthorized, or noncompliant installation; improper rigging or anchoring; deficient utility or medical-gas connections; incorrect exhaust routing; inadequate ventilation, grounding, electrical supply, air quality, oxygen supply, alarms, fire protection, room construction, or other site conditions; or acts or omissions of contractors, distributors, purchasers, facilities, or inspectors.

No chamber may be placed into clinical service until all required installation steps, inspections, tests, acceptance criteria, documentation, permits, and training have been completed and the facility has established lawful clinical and emergency operations. Operating before commissioning or after a failed test is prohibited.

14. Training, Competency, and Staffing

Receipt of a chamber, a demonstration, a manual, a certificate of attendance, or access to educational content does not by itself establish operator competency or satisfy all legal, accreditation, insurer, employer, or professional requirements. The facility is responsible for selecting qualified staff; verifying licenses and credentials; providing model-specific initial and recurrent training; documenting competency; supervising trainees; conducting drills; and restricting access to authorized personnel.

The facility must maintain staffing sufficient to operate the chamber safely, continuously observe and communicate with occupants as required, respond to emergencies, prevent unauthorized access, and meet the chamber classification, facility policy, and applicable code. The Company is not liable for negligent hiring, inadequate staffing, insufficient supervision, lapsed credentials, failed competency, or deviation from training by a distributor, facility, operator, clinician, or other person.

15. Safe Operation and Operator Responsibilities

The owner, facility, medical director, safety director, treating practitioner, chamber operator, and other personnel each remain responsible for the duties assigned to them by law, professional standards, facility policy, and the product documents. Before every treatment, authorized personnel must verify chamber readiness, required inspections, communications, emergency systems, prescribed treatment parameters, patient identity and screening, prohibited-item controls, oxygen-delivery equipment, and any other checklist item required by current instructions.

Operators must remain within required attendance and observation positions; monitor chamber and patient conditions; respond to alarms or abnormal conditions; follow compression, treatment, decompression, and emergency procedures; and document operations, maintenance, incidents, and deviations. Safety systems, interlocks, relief devices, alarms, communications, valves, monitors, or protective features may never be defeated, obstructed, silenced without cause, or bypassed.

The Company is not liable for injury, death, property damage, loss, interruption, or other harm caused by misuse; operator error; unauthorized access; lack of supervision; failure to screen or monitor; incorrect pressure, oxygen dose, compression or decompression rate; failure to follow a medical order; prohibited items; failure to respond to alarms; operation outside specifications; or any other use contrary to the labeling, manuals, warnings, training, or applicable law.

16. Oxygen, Fire, Pressure, and Environmental Hazards

Hyperbaric systems involve elevated pressure and may involve oxygen-enriched atmospheres or high-concentration oxygen. These conditions can intensify combustion and create serious risks including fire, explosion, barotrauma, decompression injury, oxygen toxicity, gas embolism, mechanical injury, and death. These risks require strict compliance with equipment instructions, prohibited-item controls, medical-gas requirements, grounding and bonding, ventilation and exhaust requirements, oxygen monitoring where required, fire-safety procedures, housekeeping, clothing and linen requirements, and emergency planning.

No ignition source, prohibited electrical or battery-powered item, flammable or combustible material, petroleum product, unapproved cosmetic, warming device, or other prohibited item may enter or be used in the chamber. Only equipment, materials, and patient-care items approved for the specific hyperbaric environment may be used. The facility is responsible for screening every person and item before entry and for enforcing its prohibited-items policy without exception.

Compressed air, medical oxygen, piping, hoses, regulators, masks, hoods, breathing systems, exhaust systems, and related components must meet applicable specifications and be installed, maintained, handled, and used by qualified personnel. The Company is not responsible for contaminated or inadequate gas supplies, nonapproved gas equipment, improper oxygen handling, facility gas-system defects, or failure to route exhaust as required.

17. Patient Selection, Screening, Monitoring, and Emergency Care

The treating practitioner and facility are solely responsible for determining medical necessity, indications, contraindications, precautions, informed consent, treatment parameters, medication management, fitness to undergo pressure, and the type and level of monitoring and emergency support required. Website content is not a substitute for a patient-specific evaluation.

The facility must maintain written normal and emergency procedures; appropriate medical oversight; required resuscitation and emergency equipment; trained personnel; communications; evacuation plans; fire procedures; and arrangements for escalation and emergency medical services. It must conduct and document drills at the frequency required by law, standards, policy, and risk assessment.

The Company is not liable for clinical judgment, diagnosis, treatment selection, informed-consent deficiencies, patient non-disclosure, inadequate screening, contraindications, medication decisions, failure to monitor, delayed emergency response, or any act or omission constituting the practice of medicine or another regulated profession by persons other than the Company.

18. Maintenance, Inspection, Service, and Records

The owner and operator must keep the chamber within its approved service life and operating limits and perform all daily, periodic, preventive, and corrective maintenance, inspection, calibration, cleaning, and testing required by the current product documents, data plate, applicable standards, law, authority having jurisdiction, insurer, and written service program. Required records must be accurate, complete, legible, retained for the applicable period, and made available to authorized service personnel and regulators as required.

Only trained and authorized service personnel may open, adjust, repair, replace, calibrate, or test components identified as service-restricted. Only Company-approved parts, materials, lubricants, cleaners, seals, windows, controls, valves, software, and procedures may be used. Maintenance intervals are maximum intervals, not permission to continue using equipment that shows damage, abnormal operation, overdue service, failed inspection, contamination, corrosion, leakage, cracking, crazing, discoloration, impact, or other unsafe condition.

If a required inspection or maintenance item is overdue, a safety device fails, damage is suspected, a warning appears, performance changes, or the chamber operates abnormally, the chamber must be removed from service and secured against use until evaluated and released by qualified authorized personnel. The Company is not liable for harm caused by deferred maintenance, incomplete records, unauthorized service, continued operation after a warning or failed test, or failure to follow a stop-use instruction.

19. Alterations, Repairs, Relocation, and Third-Party Components

No person may modify, weld, drill, cut, machine, reprogram, bypass, relocate, re-rate, repaint in a manner affecting safety, or otherwise alter the chamber, pressure boundary, windows, penetrations, piping, controls, software, safety devices, electrical system, oxygen system, or labeling without prior written Company authorization and completion of all required engineering, regulatory, inspection, and documentation steps.

Accessories, monitors, communications equipment, entertainment equipment, patient-care devices, breathing systems, medical-gas components, furniture, mattresses, linens, cleaning agents, and other items must be approved for the specific model and hyperbaric environment. Compatibility or approval of one item, model, or configuration does not imply approval of another.

Any unauthorized modification, repair, relocation, substitution, integration, or use of a third-party component may create a serious hazard, invalidate certification or clearance-related assumptions, void warranty coverage to the extent permitted by law, and require new review or testing. The Company disclaims liability for any resulting harm to the maximum extent permitted by law.

20. Cleaning, Infection Control, and Chemical Exposure

The facility is responsible for cleaning, disinfection, infection prevention, linen handling, waste management, and environmental controls appropriate to its patients and operations. Only products and methods approved in current Company instructions may be used on acrylic, seals, coatings, controls, breathing systems, or other chamber components. Harsh chemicals, incompatible disinfectants, abrasive materials, ultraviolet exposure, direct heat, and unapproved products can degrade materials and create latent hazards.

The Company is not liable for infection transmission, residue, material degradation, cracking, crazing, discoloration, fire risk, seal failure, or other harm caused by facility infection-control practices, unapproved chemicals or methods, inadequate drying or ventilation, or failure to inspect after exposure.

21. Safety Complaints, Suspected Malfunctions, and Adverse Events

Routine questions and service requests must be reported promptly to the distributor of record with the chamber model, serial number, facility contact, description of the issue, operating conditions, relevant logs, photographs if safe to obtain, and any other requested information. Do not continue operating a chamber that may be unsafe merely because a response is pending.

A suspected device malfunction, serious injury, death, fire, pressure-vessel event, oxygen incident, entrapment, uncontrolled compression or decompression, failure of a safety system, or other urgent safety concern should be reported immediately to the distributor and to the Company at 602-737-1160. Call 911 or the local emergency number first when emergency assistance is needed. Preserve the device, settings, components, labels, records, and other evidence except when alteration is necessary to protect life or prevent further harm.

No provision of these Terms prohibits or discourages any person from reporting a safety concern to FDA, another regulator, an authority having jurisdiction, or emergency services. Distributors and facilities must cooperate with complaint investigation, medical-device reporting, field action, inspection, and record-preservation requirements. The Company may contact involved parties directly when necessary to investigate a complaint, protect safety, or meet legal obligations.

22. Safety Notices, Corrections, and Recalls

The purchaser, distributor, owner, and facility must maintain current contact, location, ownership, and serial-number information and promptly notify the distributor of changes. They must receive, review, distribute, implement, and document all safety notices, labeling updates, service bulletins, corrections, stop-use notices, and recalls applicable to the chamber.

A chamber subject to a stop-use instruction, correction, or recall must be secured and handled exactly as directed. Resale, transfer, export, relocation, or disposal does not eliminate continuing safety obligations. Failure to maintain traceability or implement a safety action may result in serious injury or death and relieves the Company of responsibility to the maximum extent permitted by law for harm caused by that failure.

23. Resale, Transfer, Relocation, and Decommissioning

Before a chamber is resold, leased, donated, transferred, relocated, recommissioned, exported, decommissioned, or disposed of, the owner must contact the distributor to determine applicable inspection, service, documentation, regulatory, warranty, installation, training, and safety requirements. The owner must disclose known damage, modifications, service history, safety notices, and operating limitations to any prospective recipient.

No Website statement confirms that a used, relocated, altered, or previously decommissioned chamber remains serviceable or compliant. A qualified evaluation, current records, approved site plan, authorized installation, acceptance testing, and training may be required before further use. Data plates, labels, serial numbers, warnings, and traceability records must not be removed or altered.

24. Limited Warranties and Warranty Administration

Any Company limited warranty applies only if stated in a separate written warranty issued for the applicable chamber, component, and transaction. That written warranty, together with any controlling distributor agreement, governs its beneficiaries, term, coverage, exclusions, claim procedure, remedies, transferability, and limitations. Website content, oral statements, demonstrations, marketing materials, distributor promises, and course materials do not create or enlarge a Company warranty.

The distributor is responsible for delivering and explaining the warranty documents applicable to its customer and for administering first-line warranty communications. A distributor may offer its own warranty or service plan, but the Company is not responsible for any distributor warranty, promise, remedy, or service obligation that exceeds or differs from the Company's signed written commitment.

Except for an express written warranty applicable to a specific product and claimant, and to the maximum extent permitted by law, the Company disclaims all implied warranties arising from Website use or third-party transactions, including implied warranties of merchantability, fitness for a particular purpose, title, noninfringement, uninterrupted operation, course of dealing, usage of trade, and any warranty that a chamber will produce a particular clinical, operational, financial, or reimbursement result. Some jurisdictions do not allow certain disclaimers, so these exclusions apply only to the extent permitted.

Warranty coverage does not extend, to the extent stated in the applicable warranty and permitted by law, to harm caused by misuse; normal wear; accident; impact; environmental exposure; inadequate utilities; improper shipping, storage, rigging, installation, integration, commissioning, operation, cleaning, maintenance, service, repair, or relocation; overdue inspection; unauthorized modification; nonapproved parts or chemicals; code violations; failure to follow instructions; or acts or omissions of a distributor, carrier, contractor, facility, clinician, operator, patient, or other third party.

25. Website Provided As Is

THE WEBSITE AND ALL WEBSITE CONTENT ARE PROVIDED "AS IS" AND "AS AVAILABLE." TO THE MAXIMUM EXTENT PERMITTED BY LAW, THE COMPANY DISCLAIMS ALL WARRANTIES REGARDING THE WEBSITE, WHETHER EXPRESS, IMPLIED, STATUTORY, OR OTHERWISE, INCLUDING ACCURACY, COMPLETENESS, TIMELINESS, AVAILABILITY, SECURITY, NONINTERFERENCE, MERCHANTABILITY, FITNESS FOR A PARTICULAR PURPOSE, TITLE, AND NONINFRINGEMENT. THE COMPANY DOES NOT WARRANT THAT THE WEBSITE WILL BE UNINTERRUPTED, ERROR-FREE, FREE OF HARMFUL CODE, OR SUITABLE FOR YOUR PURPOSE.

Regulatory status, standards, product configurations, and legal requirements may change. You are responsible for verifying current information through controlling product documents, the distributor, qualified professionals, regulators, and authorities having jurisdiction before relying on it.

26. Limitation of Liability

TO THE MAXIMUM EXTENT PERMITTED BY LAW, THE COMPANY AND ITS MEMBERS, MANAGERS, OFFICERS, EMPLOYEES, REPRESENTATIVES, AND AFFILIATES WILL NOT BE LIABLE FOR ANY INDIRECT, INCIDENTAL, SPECIAL, EXEMPLARY, PUNITIVE, OR CONSEQUENTIAL DAMAGES; LOSS OF PROFITS, REVENUE, BUSINESS, USE, DATA, GOODWILL, OPPORTUNITY, OR ANTICIPATED SAVINGS; BUSINESS INTERRUPTION; SUBSTITUTE EQUIPMENT OR SERVICES; FACILITY DELAY; LOSS OF REIMBURSEMENT; OR THIRD-PARTY CLAIMS ARISING FROM OR RELATING TO THE WEBSITE, WEBSITE CONTENT, A DISTRIBUTOR'S CONDUCT, OR A CHAMBER TRANSACTION, EVEN IF ADVISED OF THE POSSIBILITY.

TO THE MAXIMUM EXTENT PERMITTED BY LAW, THE COMPANY IS NOT LIABLE FOR HARM CAUSED BY INCORRECT OR UNAUTHORIZED SELECTION, SITE PLANNING, SHIPPING, STORAGE, RIGGING, INSTALLATION, INTEGRATION, COMMISSIONING, TRAINING, CLINICAL USE, OPERATION, CLEANING, MAINTENANCE, INSPECTION, SERVICE, REPAIR, MODIFICATION, RELOCATION, RESALE, DECOMMISSIONING, OR DISPOSAL; FAILURE TO FOLLOW LABELING OR SAFETY NOTICES; USE OUTSIDE RATED LIMITS; OR ANY ACT OR OMISSION OF A DISTRIBUTOR, CONTRACTOR, FACILITY, HEALTHCARE PROFESSIONAL, OPERATOR, PATIENT, OR OTHER THIRD PARTY.

For claims arising solely from use of the Website, the Company's aggregate liability will not exceed the greater of one hundred U.S. dollars (US $100) or the amount you paid directly to the Company, if any, specifically for Website access during the twelve months before the event giving rise to the claim. For a product claim by a party entitled to enforce a separate signed Company agreement or express written warranty, the liability limits and exclusive remedies in that controlling document apply.

These limitations do not exclude liability that cannot lawfully be excluded or limited. Nothing in these Terms releases the Company from responsibility imposed by applicable law for its own fraud, willful misconduct, gross negligence where not waivable, or a proven manufacturing defect to the extent such responsibility cannot lawfully be disclaimed. The limitations are intended to allocate risk among legally responsible parties, not to misstate nonwaivable law.

27. Indemnification

To the maximum extent permitted by law, you will defend, indemnify, and hold harmless the Company and its members, managers, officers, employees, representatives, and affiliates from claims, demands, actions, proceedings, losses, liabilities, penalties, judgments, settlements, damages, and reasonable attorneys' fees arising from or relating to: (a) your violation of these Terms; (b) your unlawful or unauthorized Website use; (c) information or materials you submit; (d) your misrepresentation of Company products or regulatory status; (e) your infringement of another person's rights; or (f) if you are a distributor, facility, commercial purchaser, owner, operator, service provider, or other commercial actor, your sales, installation, clinical, operational, service, employment, or regulatory acts or omissions.

This section does not require a consumer to indemnify the Company for the Company's own nonwaivable liability and does not override a different allocation in a signed agreement. The Company may control the defense and settlement of an indemnified matter, and you may not settle a matter that admits Company fault, imposes obligations on the Company, or restricts Company activity without prior written consent.

28. Eligibility and Acceptable Website Use

You must be at least eighteen years old and legally capable of entering a binding agreement to use interactive Website features. You may use the Website only for lawful purposes and in compliance with these Terms. You must not:

access or attempt to access nonpublic systems, accounts, data, source code, or security features;

probe, scan, test, circumvent, disable, or interfere with security, authentication, rate limits, availability, or operation; introduce malware, harmful code, automated requests, scraping tools, or excessive traffic, except ordinary search-engine indexing authorized by the Company; impersonate another person, misstate affiliation, submit false information, or use the Website to make unauthorized product or medical claims; copy, modify, republish, frame, mirror, sell, license, reverse engineer, or exploit Website content except as expressly permitted by law or written Company authorization; or use Website information to facilitate unsafe, unlawful, counterfeit, infringing, deceptive, or unauthorized device activity.

The Company may restrict or terminate Website access, preserve evidence, and cooperate with lawful investigations if it reasonably believes use is unsafe, unlawful, abusive, or inconsistent with these Terms.

29. Accounts, Forms, and Information You Submit

If the Website permits an account, request form, document upload, or other submission, you must provide accurate, current, complete information and update it as needed. You are responsible for account credentials and activity under your account and must promptly report suspected unauthorized access.

Do not submit protected health information, medical records, payment-card data, government identifiers, export-controlled data, trade secrets, or other sensitive information unless the Website expressly requests it through an appropriate secure process. A general contact form is not a medical-record system or emergency channel. You represent that you have all rights and lawful authority needed to submit information and permit the Company to use it to respond, route the inquiry, investigate a complaint, meet legal obligations, and operate the Website.

Submitting a request does not require the Company or any distributor to respond, provide a quote, accept an order, extend credit, reserve inventory, or enter a relationship. The Company may retain communications and records as permitted or required by law, its quality system, complaint-handling obligations, and its Privacy Policy.

30. Electronic Communications; No Marketing Consent by Implication

When you contact the Company electronically, you consent to receive responsive and transactional communications through the contact information you provide. Electronic records and signatures may be used to the extent permitted by law. You are responsible for keeping contact information current and for maintaining copies of communications relevant to a transaction or safety matter.

Submitting a general inquiry does not, by itself, provide any consent that applicable law requires separately for marketing calls or text messages. Any marketing consent will be requested in distinct language where required and may be withdrawn as stated in that consent or applicable law.

31. Intellectual Property

The Website, including its text, graphics, photographs, videos, designs, software, arrangement, product names, model names, logos, trademarks, service marks, and other content, is owned by or licensed to the Company and protected by intellectual-property laws. Hyperbaric for Life, Hyperbaric for Life, associated logos, and Company product identifiers may not be used without prior written permission except for truthful nominative reference permitted by law.

Subject to these Terms, the Company grants you a limited, revocable, nonexclusive, nontransferable license to access and view the Website for legitimate informational or business-evaluation purposes. No other right or license is granted by implication, estoppel, or otherwise. You may not remove copyright, trademark, patent, proprietary, regulatory, warning, or attribution notices.

32. Feedback and Nonconfidential Submissions

If you voluntarily provide an idea, suggestion, comment, or feedback about the Website or Company products without a separate written confidentiality agreement, you grant the Company a perpetual, irrevocable, worldwide, royalty-free, transferable, sublicensable license to use, reproduce, modify, disclose, and commercialize that feedback for any lawful purpose without compensation or attribution. This does not apply to a safety complaint, medical-device report, personal information governed by the Privacy Policy, or material protected by a separate signed agreement.

33. Third-Party Content, Links, and Services

The Website may link to or reference distributors, standards organizations, regulators, financing providers, publications, social-media services, or other third parties. Links are provided for convenience and do not make the third party an agent of the Company or constitute endorsement of every statement, product, service, privacy practice, security practice, or term. The Company does not control and is not responsible for third-party sites or services.

Your dealings with a distributor or other third party are between you and that party. Review the third party's contracts, warranties, privacy practices, qualifications, and representations. A listing or referral does not guarantee that a distributor remains authorized for every product, territory, or service at every time; verify current status when material.

34. Privacy

The Company's collection, use, disclosure, and retention of personal information through the Website are described in its Privacy Policy, which is incorporated into these Terms by reference. If you submit information about another person, you represent that you are authorized to do so and have provided any required notice or obtained any required consent. Product complaints and safety investigations may require collection and disclosure of information to distributors, service providers, insurers, regulators, healthcare facilities, or other parties as permitted or required by law.

35. Compliance With Laws; Anti-Corruption; Export Controls

You must comply with all laws and regulations applicable to your Website use and any chamber-related activity, including medical-device, healthcare, professional, privacy, marketing, accessibility, occupational-safety, building, fire, pressure-vessel, medical-gas, environmental, sanctions, export-control, anti-boycott, anti-bribery, and anti-kickback requirements.

No chamber, technical data, software, component, or service may be exported, reexported, transferred, or used in violation of U.S. law or applicable foreign law. You may not transact with a prohibited person, destination, or end use. You are responsible for licenses, classifications, screening, customs, taxes, import requirements, local registration, and post-market obligations outside the United States. Website availability in a location does not mean a product is authorized there.

36. Governing Law and Informal Dispute Resolution

These Terms and any dispute arising from the Website are governed by the Federal Arbitration Act where applicable and by the laws of the State of Arizona, without regard to conflict-of-law rules. The U.N. Convention on Contracts for the International Sale of Goods does not apply.

Before filing a claim concerning the Website, the claimant must send a written notice describing the claimant's name and contact information, the relevant facts, the requested relief, and supporting documents to: Hyperbaric for Life, LLC, Attn: Legal Notice, P.O. Box 217, Waddell, Arizona 85355. The parties will attempt in good faith for thirty days after receipt to resolve the matter. This requirement does not prevent immediate action for emergency injunctive relief, a safety report to a regulator, or a claim for which the limitations period would expire during the thirty-day period.

37. Binding Arbitration and Class-Action Waiver

Except for a matter eligible for small-claims court, a request for temporary or preliminary injunctive relief to protect safety or intellectual property, or a claim that applicable law makes nonarbitrable, any dispute arising out of or relating to the Website or these Terms will be resolved by binding individual arbitration administered by the American Arbitration Association under the rules applicable to the nature of the dispute. Arbitration will take place in Maricopa County, Arizona, unless applicable consumer law requires a different location or remote process. The arbitrator may award relief available in court on an individual basis and must enforce applicable statutes of limitation and valid contractual limitations.

YOU AND THE COMPANY WAIVE THE RIGHT TO A JURY TRIAL AND AGREE THAT CLAIMS MAY BE BROUGHT ONLY IN AN INDIVIDUAL CAPACITY, NOT AS A PLAINTIFF, CLASS MEMBER, OR REPRESENTATIVE IN A CLASS, COLLECTIVE, CONSOLIDATED, MASS, OR REPRESENTATIVE ACTION. The arbitrator may not consolidate claims or preside over a representative proceeding without the written consent of all affected parties. If the class-action waiver is finally held unenforceable for a particular claim, that claim must proceed in a court of competent jurisdiction and not in arbitration.

A commercial entity will pay arbitration fees as allocated by the applicable rules and award. For a consumer, the Company will bear fees to the extent required by applicable law or the applicable consumer rules. Nothing in this section prevents a person from reporting a matter to a government agency or the agency from seeking relief within its authority.

38. Court Venue for Nonarbitrable Matters

For any dispute not subject to arbitration, the parties consent to exclusive jurisdiction and venue in the state courts located in Maricopa County, Arizona, or the United States District Court for the District of Arizona, except where applicable law requires otherwise. Each party waives objections based on personal jurisdiction, venue, or inconvenient forum to the extent permitted by law.

39. Time Limit to Bring Website Claims

To the maximum extent permitted by law, a claim arising solely from Website use must be commenced within one year after the claimant knew or reasonably should have known of the facts giving rise to the claim, or it is permanently barred. This section does not shorten a limitations period that applicable law prohibits the parties from shortening and does not alter a limitations period or claim procedure in a controlling signed product agreement or written warranty.

40. Changes to the Website or These Terms

The Company may modify, suspend, or discontinue all or part of the Website at any time. It may update these Terms by posting the revised version and changing the effective or last-updated date. Changes apply prospectively when posted unless law requires additional notice or consent. Your continued Website use after an effective change constitutes acceptance. Material changes to a separate signed agreement or written product warranty can be made only as allowed by that document and are not accomplished merely by changing these Terms.

41. Suspension and Termination

The Company may suspend or terminate your access to the Website for suspected violation of these Terms, risk to safety or security, unlawful activity, or discontinuation of the Website. Upon termination, the Website license ends, but provisions that by their nature should survive will survive, including ownership, disclaimers, limitations, indemnification, dispute resolution, and record-related provisions. Termination of Website access does not terminate obligations under a separate agreement or safety notice.

42. Force Majeure

The Company is not liable for delay or failure in Website performance caused by events beyond its reasonable control, including natural disaster, fire, epidemic, war, terrorism, civil disorder, labor disruption, transportation interruption, utility or communications failure, cyberattack, supplier failure, government action, embargo, shortage, or authority having jurisdiction. This section does not excuse mandatory safety reporting, recall obligations, or duties that applicable law makes nonwaivable.

43. Assignment

You may not assign or transfer these Terms or any Website right without prior written Company consent. The Company may assign these Terms in connection with a merger, acquisition, reorganization, sale of assets, financing, affiliate transfer, or operation of law. An attempted assignment in violation of this section is void to the extent permitted by law.

44. Severability and Interpretation

If a provision is held invalid or unenforceable, it will be enforced to the maximum lawful extent and the remaining provisions will remain effective. If a class-action waiver cannot be enforced for a particular claim, Section 37 governs the treatment of that claim. Headings are for convenience only. "Including" means "including without limitation." The singular includes the plural and vice versa where context requires. These Terms will not be construed against a party merely because that party drafted them.

45. Waiver; Cumulative Remedies

A waiver must be in a writing signed by an authorized Company representative. Delay or failure to enforce a provision is not a waiver. A waiver on one occasion is not a waiver on another. Except where a remedy is expressly exclusive, rights and remedies are cumulative.

46. Entire Agreement and Order of Precedence

These Terms and the Privacy Policy are the entire agreement regarding Website use and supersede prior Website-use discussions or statements. They do not supersede a signed distributor agreement, purchase agreement, installation agreement, service agreement, confidentiality agreement, written limited warranty, product labeling, safety notice, or other product-specific document.

For matters of safe device use, current labeling, data-plate limits, manuals, and manufacturer-issued safety notices control. For a product transaction, the applicable signed commercial agreement and written warranty control. For personal-information practices, the Privacy Policy controls. For Website use not addressed in those documents, these Terms control.

47. Contact and Notices

Routine product, warranty, installation, service, and training questions must be directed to the distributor of record. To help identify the distributor, contact the Company by telephone and provide the chamber model and serial number.

Hyperbaric For Life, LLC
Doing business as Hyperbaric for Life
P.O. Box 217
Waddell, Arizona 85355
Telephone: 602-737-1160

Telephone calls do not constitute formal legal notice. Formal legal notices must be sent to the mailing address above, addressed to "Legal Notice," using a method that provides confirmation of delivery. The Company may provide notices through the Website, postal mail, or the contact information associated with an inquiry or applicable commercial record.

48. Acknowledgment

BY USING THE WEBSITE, YOU ACKNOWLEDGE THAT YOU HAVE READ AND UNDERSTOOD THESE TERMS; THAT THE WEBSITE DOES NOT CREATE A DIRECT CHAMBER SALE, INSTALLATION, SERVICE, MEDICAL, OR WARRANTY RELATIONSHIP WITH THE COMPANY; THAT ROUTINE CUSTOMER SUPPORT IS PROVIDED THROUGH THE DISTRIBUTOR OF RECORD; AND THAT HYPERBARIC CHAMBERS MUST BE SELECTED, INSTALLED, COMMISSIONED, MAINTAINED, AND OPERATED ONLY IN ACCORDANCE WITH CONTROLLING PRODUCT DOCUMENTS, APPLICABLE LAW, AND QUALIFIED PROFESSIONAL OVERSIGHT.