Data / Medical devices / Regulator, Pressure, Gas Cylinder / United States
FDA-registered makers of Regulator, Pressure, Gas Cylinder in the United States: 34 establishments
34 establishments in the United States are registered with the FDA to make Regulator, Pressure, Gas Cylinder (product code CAN). 1 has a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 2, 2026.
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- Device
- Regulator, Pressure, Gas Cylinder
- Product code
- CAN
- Country
- United States
Makers of Regulator, Pressure, Gas Cylinder 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 | 2 | April 5, 1990 | 0 | 0 | 0 | api.fda.gov |
| Ameriflo2 Incorporated | Indianapolis, IN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Angioadvancements, LLC | N Ft Myers, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Airgas Therapeutics LLC | Plumsteadville, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alcon Research, LLC | Fort Worth, TX, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Baxter Healthcare Corporation | Hayward, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bound Tree Medical, LLC | Grand Prairie, TX, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Controls Corporation Of America | Virginia Beach, VA, United States | Contract manufacturer, Manufacturer, Manufacturer for export, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Control Devices - Carr Lane | Saint Louis, MO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Doner Industries, Inc. | Rogers, AR, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Flotec, Inc. | Eagle Creek, IN, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Icu Medical, Inc. | San Clemente, CA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ICU Medical, Inc. | Dublin, OH, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Inovo Inc. | Lehigh Acres, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Integra LifeSciences Corporation | Princeton, NJ, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kmi Imi Group / Dba: Innovative Med, Inc. | Irvine, CA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Life Corporation | Orlando, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Lifeport, LLC. | Woodland, WA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Linde Gas & Equipment Inc. | Tonawanda, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Linvatec Corporation | Largo, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mada Medical Products, Inc. | Carlstadt, NJ, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDLINE INDUSTRIES, LP - Northfield | Northfield, IL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Microaire Surgical Instruments LLC | Charlottesville, VA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Micromedics, Inc. | Saint Paul, MN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ohio Medical LLC | Gurnee, IL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Pmda, LLC. | Fort Myers, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Precision Medical, Inc. | Northampton, PA, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Spiracle Technology | Los Alamitos, CA, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthcare Diagnostics Inc | East Walpole, MA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthcare Diagnostics Inc. | Tarrytown, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Synthes (USA) Products LLC | West Chester, PA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| The Harris Products Group | Gainesville, GA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Vapotherm Inc. | Exeter, NH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Western Enterprises, Inc. | Westlake, OH, United States | Manufacturer | 0 | 0 | 5 | 1 | 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.