Data / Medical devices / Apparatus, Gas-Scavenging / United States
FDA-registered makers of Apparatus, Gas-Scavenging in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Apparatus, Gas-Scavenging (product code CBN). 8 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
- Apparatus, Gas-Scavenging
- Product code
- CBN
- Country
- United States
Makers of Apparatus, Gas-Scavenging in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Precision Fluidics Division Parker Hannifin Corp. | Hatfield, PA, United States | Manufacturer | 3 | March 5, 2023 | 0 | 0 | 0 | api.fda.gov |
| Accutron, Inc. | Phoenix, AZ, United States | Manufacturer | 2 | March 12, 2004 | 0 | 0 | 0 | api.fda.gov |
| Carestream Medical | Sanford, FL, United States | Manufacturer | 2 | June 23, 2011 | 0 | 0 | 0 | api.fda.gov |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 2 | October 30, 2014 | 0 | 0 | 0 | api.fda.gov |
| Anecare LLC | Salt Lake City, UT, United States | Manufacturer, Specification developer | 1 | July 22, 2005 | 0 | 0 | 0 | api.fda.gov |
| Dynasthetics | Salt Lake City, UT, United States | Manufacturer | 1 | April 16, 2010 | 0 | 1 | 0 | api.fda.gov |
| Peace Medical, Inc. | Wharton, NJ, United States | Manufacturer | 1 | October 15, 1990 | 0 | 0 | 0 | api.fda.gov |
| Sedation Systems LLC | Tierra Verde, FL, United States | Specification developer | 1 | May 5, 2017 | 0 | 0 | 0 | api.fda.gov |
| Anesthesia Associates, Inc. | San Marcos, CA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Datex-Ohmeda, Inc. | Madison, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hda Technology, Inc. | Lake Forest, CA, United States | Contract 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.