Data / Medical devices / Mask, Gas, Anesthetic / United States
FDA-registered makers of Mask, Gas, Anesthetic in the United States: 16 establishments
16 establishments in the United States are registered with the FDA to make Mask, Gas, Anesthetic (product code BSJ). 2 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
- Mask, Gas, Anesthetic
- Product code
- BSJ
- Country
- United States
Makers of Mask, Gas, Anesthetic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Covidien | Lafayette, CO, United States | Specification developer | 1 | August 11, 1995 | 0 | 0 | 0 | api.fda.gov |
| SunMed Group Holdings, LLC | Grand Rapids, MI, United States | Complaint file establishment, Repackager or relabeler, Specification developer | 1 | October 13, 2017 | 0 | 0 | 0 | api.fda.gov |
| Anesthesia Associates, Inc. | San Marcos, CA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Doner Industries, Inc. | Rogers, AR, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Fte Dynamics, LLC | Chino Hills, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Iilabco LLC | Brea, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intersurgical Inc. | Indianapolis, IN, United States | Manufacturer | 0 | 0 | 1 | 1 | api.fda.gov | |
| Med Systems | San Diego, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mile High Medical Supplies LLC | Delta, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mercury Medical Enterprises, LLC | Clearwater, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pneuma Therapeutics, Inc. | San Marcos, CA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precision Fluidics Division Parker Hannifin Corp. | Hatfield, PA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Thermedia Corporation | Shelton, WA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Westmed, Inc. | Tucson, AZ, United States | Manufacturer, 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.