HBOT Chambers & Systems from Oxyboost
Oxyboost is a hyperbaric chamber supplier based in Kruiningen, Zeeland (Netherlands), listing soft-sided and monoplace chambers with operating pressures spanning 1.3 to 2.4 ATA across the lineup as a whole. As of July 2026, none of its certification claims could be verified against official registers - the company's sole certification statement is a manufacturer claim without any checkable standard, CE number, or FDA clearance. Its stated service area is limited to the Netherlands.
Company & Products
Oxyboost operates from Polderweg 12, 4416 RE Kruiningen, in the Dutch province of Zeeland. According to its website (retrieved 2026-07-22), the lineup covers two chamber categories - soft-sided chambers and monoplace chambers - with operating pressures spanning 1.3 to 2.4 ATA across the range as a whole. The company does not publish which pressures apply to which chamber type.
No per-model capacity figures are published, and no price range is publicly available. According to the manufacturer, chambers can be acquired through purchase, rental, or leasing - if confirmed in contract terms, that flexibility may interest operators who want to test demand before committing capital.
Certifications & Verification
This is where Oxyboost's profile is thinnest. As of 2026-07-22, no register-verified certifications are on file. The company's website claims 'medically certified technology' for a single model, the HPO TECH Horizon, but names no standard, no CE marking number, no FDA clearance, and no register entry of any kind. Without an identifier, the claim cannot be checked against FDA 510(k) or EUDAMED - it remains a manufacturer statement.
This does not prove the equipment is uncertified; it means the claim is currently unverifiable. Buyers with regulatory or insurance requirements should request the actual certificates, notified body details, and applicable standards in writing before signing anything. No documented conflicts between sources exist for this profile - the issue is absence of evidence, not contradiction.
Service & Support
All service information is manufacturer-stated. Oxyboost says it provides installation with personal instruction and on-site maintenance and service, and describes itself as accessible to customers throughout the Netherlands. There is no indication of service coverage beyond the Dutch market.
The company advertises a 'full warranty', but neither its duration nor its conditions are publicly specified. For a B2B purchase, this is a gap to close during negotiation: ask for the warranty term, what it covers, response times for on-site service, and whether the manufacturer-stated rental and leasing options include maintenance.
Who It Suits
The published data supports only a narrow assessment. Oxyboost lists two chamber categories and a lineup-wide pressure span of 1.3 to 2.4 ATA, but does not state which pressures, capacities, or specifications belong to which chamber type. Buyers therefore cannot match a specific model to a specific use case from public information alone - a per-model specification sheet is the first document to request.
Since no medical device certification is register-verified for any Oxyboost model, buyers with clinical or otherwise regulated use cases should treat certification documentation as a precondition, not a formality. The manufacturer-stated Netherlands-only service area makes Oxyboost primarily relevant for Dutch buyers who value local installation and on-site support.
Every data point on this profile is source-checked. Certifications are only marked as verified when confirmed in official registers - never on manufacturer claims alone.
- FDA 510(k) database
- EUDAMED registry
- Manufacturer filings