HBOT Chambers & Systems from HPO Tech

Certifications & Verification

One item is register-verified: HPO Tech holds an active EUDAMED manufacturer registration under SRN TR-MF-000032522, confirming its formal registration as a device manufacturer in the EU database.

Everything else is manufacturer-stated and could not be checked against public registers: CE marking (MDD 93/42/EEC / MDR 2017/745), UKCA, ASME PVHO, an ASME U-Stamp (BPVC Sec. VIII Div. 1), PED, NFPA compliance, and ISO 13485, 9001, 14001, 45001, and 27001. The company also lists national approvals per its own statements: Medsafe (New Zealand), Thai FDA, FDA Ghana, Saudi SFDA, and UAE MOHAP/EDE.

On the US market the sources disagree. The manufacturer's about-us page references an 'FDA clearance status that varies by chamber model', but the FDA 510(k) database returns no records for the applicant as of 2026-07-22. This profile therefore lists no US FDA clearance.

Service, Support & Warranty

Per its official brochure, HPO Tech delivers turn-key: installation plus regular maintenance services, staff training, system service, and 24/7 real-time remote support ('When you acquire our hyperbaric systems, we become your partner'). Service is offered worldwide from the Istanbul manufacturing base.

The brochure claims 'lifetime warranties' as part of its long-term client support, but no concrete written warranty terms or durations are published on the product pages - buyers should request these in writing before purchase.

Reference installations, all per the manufacturer: the Washington Commanders (NFL, USA), Fairmont Hotel Mumbai (India), Repose Space, the Sharjah Amiri Guards (UAE), and a TROJAN 2.0 ATA installation at NUMA Clinic London (UK).

Who It Suits

The line-up points at professional facilities. Monoplace and multiplace chambers reaching 6.0 ATA and up to 12 patient seats are clinic- and hospital-scale equipment; the product data reviewed for this profile lists only these two chamber types, so any other formats would need to be confirmed with the manufacturer directly.

The manufacturer's own reference list - a pro sports franchise, a hotel, a clinic, and a state security force - matches that positioning: operators who need multi-seat throughput or pressures above the wellness range. Buyers who require US-market regulatory clearance should note the absence of any FDA 510(k) record as of 2026-07-22.