Data / Medical devices / Generator, Oxygen, Portable / United States
FDA-registered makers of Generator, Oxygen, Portable in the United States: 24 establishments
24 establishments in the United States are registered with the FDA to make Generator, Oxygen, Portable (product code CAW). 20 have a 510(k) clearance or PMA approval on file and 8 have a recall event. FDA data exported November 2, 2026.
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- Device
- Generator, Oxygen, Portable
- Product code
- CAW
- Country
- United States
Makers of Generator, Oxygen, Portable in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| 3B Medical Inc | W Jefferson, OH, United States | Manufacturer | 9 | September 29, 2025 | 0 | 0 | 0 | api.fda.gov |
| Caire Inc. | Ball Ground, GA, United States | Repackager or relabeler, Specification developer | 9 | July 11, 2025 | 0 | 4 | 0 | api.fda.gov |
| Caire Inc. | Ball Ground, GA, United States | Manufacturer, Repackager or relabeler | 8 | July 11, 2025 | 0 | 0 | 0 | api.fda.gov |
| Ventec Life Systems, Inc. | Bothell, WA, United States | Complaint file establishment, Manufacturer, Specification developer | 6 | August 6, 2020 | 0 | 0 | 0 | api.fda.gov |
| DeVilbiss Healthcare LLC. | Somerset, PA, United States | Manufacturer | 5 | March 26, 2026 | 0 | 5 | 0 | api.fda.gov |
| Inogen, Inc. | Goleta, CA, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 5 | June 30, 2023 | 0 | 1 | 0 | api.fda.gov |
| Inogen, Inc | Plano, TX, United States | Manufacturer | 4 | June 30, 2023 | 0 | 0 | 0 | api.fda.gov |
| On Site Gas Systems, Inc. | Newington, CT, United States | Manufacturer | 4 | January 7, 2010 | 0 | 1 | 0 | api.fda.gov |
| Allied Medical LLC | Earth City, MO, United States | Manufacturer | 3 | March 19, 1993 | 0 | 0 | 0 | api.fda.gov |
| Nidek Medical Products, Inc. | Birmingham, AL, United States | Manufacturer, Manufacturer for export | 3 | May 7, 2020 | 0 | 1 | 1 | api.fda.gov |
| Pacific Consolidated Industries, LLC | Riverside, CA, United States | Manufacturer | 3 | January 21, 2011 | 0 | 1 | 0 | api.fda.gov |
| Respironics Inc. | Murrysville, PA, United States | Complaint file establishment, Manufacturer, Specification developer | 3 | November 4, 2011 | 0 | 1 | 0 | api.fda.gov |
| Life Corporation | Orlando, FL, United States | Repackager or relabeler, Specification developer | 2 | April 23, 2026 | 0 | 0 | 0 | api.fda.gov |
| Precision Medical, Inc. | Northampton, PA, United States | Manufacturer | 2 | July 1, 2011 | 0 | 0 | 0 | api.fda.gov |
| Airsep Corp. | Buffalo, NY, United States | Manufacturer, Manufacturer for export | 1 | March 28, 2011 | 0 | 0 | 0 | api.fda.gov |
| Avox Systems | Lancaster, NY, United States | Manufacturer | 1 | July 24, 2012 | 0 | 0 | 0 | api.fda.gov |
| O2 Concepts, LLC | Middlebury, CT, United States | Manufacturer | 1 | December 20, 2018 | 0 | 0 | 0 | api.fda.gov |
| Oxus America, Inc. | Orion Township, MI, United States | Complaint file establishment, Manufacturer | 1 | May 31, 2023 | 0 | 1 | 0 | api.fda.gov |
| Respironics, Inc. | New Kensington, PA, United States | Manufacturer | 1 | November 4, 2011 | 0 | 0 | 0 | api.fda.gov |
| Westmed, Inc. | Tucson, AZ, United States | Manufacturer | 1 | December 28, 1995 | 0 | 0 | 0 | api.fda.gov |
| Creative Foam Corporation dba MT. OLIVE MFG | Mooresville, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Novair USA Corp. | North Tonawanda, NY, United States | Manufacturer for export | 0 | 0 | 0 | 0 | api.fda.gov | |
| ResMed Corp | Lithia Spgs, GA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ventec Life Systems, Inc. | Woodinville, WA, United States | Manufacturer | 0 | 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.