Data / Medical devices / Chamber, Hyperbaric / United States
FDA-registered makers of Chamber, Hyperbaric in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Chamber, Hyperbaric (product code CBF). 10 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Chamber, Hyperbaric
- Product code
- CBF
- Country
- United States
Makers of Chamber, Hyperbaric in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Perry Baromedical Corporation | Riviera Beach, FL, United States | Manufacturer | 10 | August 13, 2010 | 0 | 0 | 0 | api.fda.gov |
| Pcci, Inc | Alexandria, VA, United States | Manufacturer | 6 | August 19, 2011 | 0 | 0 | 0 | api.fda.gov |
| Hyperbaric Modular Systems, Inc. | San Diego, CA, United States | Manufacturer | 4 | March 22, 2017 | 0 | 0 | 0 | api.fda.gov |
| Sechrist Industries, Inc. | Anaheim, CA, United States | Complaint file establishment, Manufacturer | 4 | May 30, 2014 | 0 | 1 | 0 | api.fda.gov |
| Hyperbaric For Life LLC | Waddell, AZ, United States | Manufacturer | 1 | November 15, 2004 | 0 | 0 | 0 | api.fda.gov |
| Hyperbaric Technologies, Inc. | Amsterdam, NY, United States | Complaint file establishment, Manufacturer | 1 | August 2, 2000 | 0 | 0 | 0 | api.fda.gov |
| Sea-Long Medical Systems, LLC | Waxahachie, TX, United States | Manufacturer | 1 | May 16, 2001 | 0 | 0 | 0 | api.fda.gov |
| Summit to Sea, LLC. | Mound, MN, United States | Manufacturer | 1 | February 8, 2008 | 0 | 0 | 0 | api.fda.gov |
| Typhoon Water Wares | Pocomoke City, MD, United States | Manufacturer | 1 | November 17, 2005 | 0 | 0 | 0 | api.fda.gov |
| Us Hyperbaric Network LLC | Sunrise, FL, United States | Specification developer | 1 | May 4, 2023 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.