Data / Medical devices / United States / Us Hyperbaric Network LLC
Us Hyperbaric Network LLC: FDA-registered device maker in Sunrise, FL, United States, 1 510(k) clearance
Us Hyperbaric Network LLC is registered with the FDA (registration 3016467917) in Sunrise, FL, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 4, 2023. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3016467917
- Address
- 789 Shotgun Road SUITE 101, Sunrise, FL, United States, 33326
- Owner or operator
- US HYPERBARIC NETWORK LLC (10062499)
- Roles
- Specification developer
- First device listed
- December 12, 2023
- Registered through
- 2026
- Brand names listed
- 430+
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Chamber, Hyperbaric | CBF | 2 | Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| May 4, 2023 | K220290 | Revitalair 430+ | CBF | Substantially Equivalent | Us Hyperbaric Network | accessdata.fda.gov |
Compare with other makers
Updated May 4, 2023. 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.