Revitalair 430F hyperbaric chamber
Clinical GradeFDA ClearedCE

Biobarica

Revitalair 430F

Dual FDA clearances200+ center franchise networkglobal regulatory approvals

Overview

The Biobarica Revitalair 430F is an FDA-cleared (K171899, K220290) hard-shell monoplace chamber designed for clinical use. Biobarica operates a global franchise network of over 200 centers, making it one of the most widely deployed clinical HBOT systems. Based in Buenos Aires, Argentina, the company has regulatory approvals across multiple countries.

Who is this for?

Designed for medical and clinical HBOT facilities that require a dependable, certified hard-shell chamber for patient treatment programs. Whether you're establishing a new hyperbaric program or upgrading aging equipment, the Revitalair 430F is built to the specifications that clinical practitioners expect at 1.45 ATA. It covers the pressure ranges required for most approved indications, making it a practical and proven choice for facilities that need performance over novelty.

Estimated Price

$30,000 - $50,000 (estimated)

Financing: Franchise/network model available

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Quick Specs

Key technical specifications

Chamber TypeHard-Shell Monoplace
Performance TierClinical Grade
Max Pressure1.45 ATA
Oxygen Deliverymask/cannula
O₂ ConcentrationUp to 95% via concentrator
Capacity1-person
Portabilityfixed-installation
Weight315 lbs
PowerStandard facility power
Warranty2 years
Ships ToGlobal (network of 200+ centers worldwide)
Made InArgentina
Brand Est.2009
FDA Cleared#K171899, K220290CE
Clinical Credibility Score6/10

Manufacturer

Brand

Biobarica

Headquarters

Buenos Aires, Argentina

Established

2009

Type

manufacturer

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Data confidence: medium · Verified 2026-03-03