Data / Medical devices / Conserver, Oxygen / United States
FDA-registered makers of Conserver, Oxygen in the United States: 10 establishments
10 establishments in the United States are registered with the FDA to make Conserver, Oxygen (product code NFB). 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
- Conserver, Oxygen
- Product code
- NFB
- Country
- United States
Makers of Conserver, Oxygen in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Inovo Inc. | Lehigh Acres, FL, United States | Manufacturer, Specification developer | 6 | December 8, 2011 | 0 | 1 | 0 | api.fda.gov |
| Responsive Respiratory Inc. | Saint Louis, MO, United States | Complaint file establishment, Remanufacturer, Repackager or relabeler, Specification developer | 3 | July 24, 2025 | 0 | 0 | 0 | api.fda.gov |
| Allied Medical LLC | Earth City, MO, United States | Specification developer | 1 | February 16, 1996 | 0 | 0 | 0 | api.fda.gov |
| Caire Inc. | Ball Ground, GA, United States | Manufacturer | 1 | December 2, 1987 | 0 | 0 | 0 | api.fda.gov |
| Caire Inc. | Ball Ground, GA, United States | Specification developer | 1 | December 2, 1987 | 0 | 0 | 0 | api.fda.gov |
| Dynasthetics | Salt Lake City, UT, United States | Manufacturer | 1 | December 15, 2022 | 0 | 0 | 0 | api.fda.gov |
| Incoba LLC Dba Dynaris | Chesterfield, MO, United States | Manufacturer | 1 | November 14, 2020 | 0 | 0 | 0 | api.fda.gov |
| Precision Medical, Inc. | Northampton, PA, United States | Manufacturer | 1 | August 25, 2003 | 0 | 0 | 0 | api.fda.gov |
| Salter Labs | El Paso, TX, United States | Specification developer | 1 | March 11, 2016 | 0 | 0 | 0 | api.fda.gov |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Specification developer | 1 | May 2, 2003 | 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.