FDA applicant

Hyperbaric Technologies, Inc.

Mccordsville, IN2 decisions2000–20020 recalls

FDA records 2 decisions for Hyperbaric Technologies, Inc. (Mccordsville, IN) from 2000 to 2002: 2 510(k) clearances. All are in product code CBF (Chamber, Hyperbaric). Its devices cite 4 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, anesthesiology panel, where it files most

How often FDA has decided Hyperbaric Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Hyperbaric Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Hyperbaric Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hyperbaric Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Hyperbaric”

FDA records each applicant name separately; these may or may not be the same firm.

Hyperbaric Aerobics, Ltd. 1 Hyperbaric Oxygen Therapy, Inc. 1 Hyperbaric America, LLC 1 Hyperbaric For Life, LLC 1

Hyperbaric Technologies, Inc.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Hyperbaric”