Data / Medical devices / Compressor, Air, Portable / United States
FDA-registered makers of Compressor, Air, Portable in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Compressor, Air, Portable (product code BTI). 9 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Compressor, Air, Portable
- Product code
- BTI
- Country
- United States
Makers of Compressor, Air, Portable in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Allied Medical LLC | Earth City, MO, United States | Manufacturer, Specification developer | 6 | November 19, 2008 | 0 | 0 | 0 | api.fda.gov |
| Precision Medical, Inc. | Northampton, PA, United States | Manufacturer | 2 | October 28, 1994 | 0 | 0 | 0 | api.fda.gov |
| Covidien | Carlsbad, CA, United States | Complaint file establishment, Specification developer | 1 | December 15, 2004 | 0 | 0 | 0 | api.fda.gov |
| DeVilbiss Healthcare LLC. | Somerset, PA, United States | Manufacturer, Repackager or relabeler | 1 | September 30, 1993 | 0 | 0 | 0 | api.fda.gov |
| Monaghan Medical Corp. | Plattsburgh, NY, United States | Manufacturer | 1 | October 24, 2013 | 0 | 0 | 0 | api.fda.gov |
| Nidek Medical Products, Inc. | Birmingham, AL, United States | Manufacturer | 1 | May 3, 2002 | 0 | 0 | 0 | api.fda.gov |
| Oricare Inc. | Quakertown, PA, United States | Specification developer | 1 | August 10, 2012 | 0 | 0 | 0 | api.fda.gov |
| Pari Respiratory Equipment, Inc. | Midlothian, VA, United States | Manufacturer, Repackager or relabeler, Specification developer | 1 | March 13, 2001 | 0 | 0 | 0 | api.fda.gov |
| Vortran Medical Technology 1, Inc. | Sacramento, CA, United States | Manufacturer | 1 | November 19, 2008 | 0 | 0 | 0 | api.fda.gov |
| Datex-Ohmeda, Inc. | Madison, WI, United States | Manufacturer, Specification developer | 0 | 0 | 1 | 1 | api.fda.gov | |
| Lifeport, LLC. | Woodland, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Respironics Inc. | Murrysville, PA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Welch Allyn, Inc. | Skaneateles Falls, NY, United States | Specification developer | 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.