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AUREVIA OXY//HOME · Powered by NuraProof

Pressure. Oxygen. Precision.

OXY//HOME reimagines the hyperbaric experience as a professionally installed, technology-led system created for sophisticated residential environments. A Scandinavian-inspired enclosure conceals advanced pressure, air-management, oxygen-delivery and safety architecture — connected through NuraProof for controlled onboarding, session oversight and long-term system care.

Development concept. Final specifications, availability and regulatory status remain subject to engineering and market approval. Images depict a product design concept.

AUREVIA OXY//HOME product design concept, installed in a luxury residential wellness room
Two configurations

Signature for the home. Clinical for the clinician.

Development Concept
AOH-130-SIG

OXY//HOME Signature

Up to 1.3 ATA

Premium home-installed system. Chamber pressurised with filtered air; oxygen delivered through an approved external-source mask or hood.

US$54,900
Founding launch price · US$64,900 RRP
Regulatory and engineering development
AOH-200-CLN

OXY//HOME Clinical

Up to 2.0 ATA

Professional or advanced home-care environment. Medical oxygen delivery, external scavenging, on-site trained supervision and local regulatory approval required.

From US$109,000
Quote-only · Clinician-directed configuration

Hyperbaric chambers are regulated medical devices in many jurisdictions. Medical clearance, trained supervision, installation controls and prescription requirements may apply. Not marketed as FDA approved, FDA cleared, medical grade or clinically proven.

OXY//HOME concept in a Scandinavian wellness suite with natural light and warm materials
Design language

Medical engineering without the institutional appearance.

Soft continuous surfaces, warm pearl-white exterior, champagne-silver metal detailing and a panoramic smoked canopy. Fire-rated exterior timber-look detailing and a light oak-coloured plinth complete a Scandinavian-inspired industrial design language that integrates into premium residential architecture.

Decorative wood and wood-look elements remain outside the pressure vessel and oxygen-delivery pathway. Unapproved combustible materials and ordinary domestic textiles do not enter the pressurised environment.

Pressure-vessel architecture

Designed from safety outward.

The chamber is intended to be pressurised with filtered air while oxygen is delivered through an approved breathing interface. This architecture is intended to reduce uncontrolled oxygen enrichment within the chamber compared with filling the entire chamber with oxygen.

Proposed engineering architecture requiring final verification
  • Rigid pressure vessel
  • Panoramic pressure-rated acrylic canopy
  • Filtered-air pressurisation
  • External oxygen source
  • Mask or hood-based oxygen delivery
  • Exhaled-oxygen scavenging pathway
  • Independent pressure regulation
  • Mechanical pressure-relief systems
  • Controlled decompression
  • External equipment & power cabinet
  • Internal components limited to pressure-rated approved materials
  • Redundant emergency decompression
Proposed AUREVIA differentiating technologies

Never-ordinary technology, safely externalised.

Zero-Lithium Interior™

Processing, power and wireless systems stay in the external cabinet. No consumer phones, tablets, headphones, smartwatches or portable batteries inside the pressurised environment.

OxySafe Atmosphere Guardian™

Validated sensors continuously monitor chamber pressure, oxygen, CO₂, CO, temperature, humidity, compressor and room ventilation — with automatic interlocks.

DualLoop Pressure Architecture™

Primary digital control plus an independent mechanical protection loop: relief valve, secondary regulator, and power-independent controlled decompression. Software cannot defeat the mechanical safety system.

EarEase Adaptive Compression™

Gradual compression, user-requested pauses, slower ramp zones and equalisation guidance. Emergency stop is never overridden.

RoomSafe Installation Intelligence™

Verifies ambient oxygen, ventilation, clearance, cabinet airflow, power, grounding and operator presence before every session.

Guardian Presence™

An authenticated, trained operator authorises and supervises every session. No fully autonomous clinical mode.

OxyOS Digital Twin™

Virtual technical profile per unit — pressure cycles, compressor hours, sensor drift, seal performance, service history — powering predictive maintenance.

Session Black Box™

Encrypted, append-only session record for user, clinician, service and regulatory review.

CalmScape Fibre-Optic Environment™

Fibre-optic ambient light, external audio and pressure-compatible acoustic transducers replace consumer electronics inside the chamber.

NuraProof connected experience

The chamber manages pressure. NuraProof manages the experience.

Onboarding, medical screening, clinician authorisation, operator assignment and long-term system care live inside a dedicated NuraProof OXY//HOME module. Users only see controls authorised for their role — arbitrary pressure or oxygen profiles cannot be created.

User onboarding
Account · chamber registration · identity verification · medical screening · clinician authorisation · trained operator · safety education · site setup
Clinician portal
Review screening · approve or decline · select approved protocol · set maximum pressure, duration, ramp rates · pause future sessions
Operator portal
Pre-use checklist · verify prohibited items removed · verify room safety · start approved sessions · monitor · stop · post-session checks
Session dashboard
Installed chamber · service & filter status · clinician approval · approved protocols · session history · operator assignment · safety notifications
OXY//HOME concept installed in a private home performance and recovery environment
Pre-session safety gate

Every session begins with a digital checklist.

The system does not make independent diagnoses. Where a safety answer requires professional assessment the session is blocked, the reason displayed, the clinician escalated and the block recorded. Bypass is not available without appropriate authority.

Respiratory symptoms · ear pain · sinus congestion · fever
Recent surgery · medication changes · pregnancy where relevant
Seizure history · lung disease · untreated pneumothorax
Implanted devices · claustrophobia
Alcohol or recreational-drug use
Flammable products · skin & hair products
Clothing material · electronic items · batteries
Watches · jewellery · hearing aids · contact lenses
Matches or lighters — strictly prohibited
Technical specification targets

Specifications, transparently provisional.

All targets remain provisional and subject to final engineering and regulatory validation.

Operating pressureUp to 1.3 ATA (Signature) · Up to 2.0 ATA (Clinical)
Pressurisation mediumFiltered air
Oxygen deliveryExternal-source approved mask or hood
OccupancyOne adult, reclined or flat
Pressure vesselRigid shell · panoramic pressure-rated acrylic canopy
Internal electronicsRestricted, externally powered
Consumer batteries insideProhibited
Pressure controlDigital primary + independent mechanical backup
Emergency decompressionInternal and external
MonitoringChamber & room O₂, CO₂, temperature, humidity, compressor, filter (all target)
Overall dimensions≈ 245 × 110 × 125 cm · console ≈ 65 cm
Installed weight550–900 kg (pressure architecture dependent)
InstallationProfessional only · site assessment required
User operationSupervised only
NuraProof connectionIncluded
White-glove installation & service

Request a site assessment.

OXY//HOME is a professionally installed residential system, not a portable device. Our team reviews room ventilation, clearance, floor loading, electrical supply and supervision arrangements before any priority-register conversion.