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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

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Allied Medical LLCEarth City, MO, United StatesManufacturer2April 5, 1990000api.fda.gov
Ameriflo2 IncorporatedIndianapolis, IN, United StatesManufacturer0000api.fda.gov
Angioadvancements, LLCN Ft Myers, FL, United StatesSpecification developer0000api.fda.gov
Airgas Therapeutics LLCPlumsteadville, PA, United StatesManufacturer0000api.fda.gov
Alcon Research, LLCFort Worth, TX, United StatesSpecification developer0000api.fda.gov
Baxter Healthcare CorporationHayward, CA, United StatesManufacturer0000api.fda.gov
Bound Tree Medical, LLCGrand Prairie, TX, United StatesManufacturer0000api.fda.gov
Controls Corporation Of AmericaVirginia Beach, VA, United StatesContract manufacturer, Manufacturer, Manufacturer for export, Remanufacturer, Repackager or relabeler, Reprocessor, Specification developer0000api.fda.gov
Control Devices - Carr LaneSaint Louis, MO, United StatesManufacturer0000api.fda.gov
Doner Industries, Inc.Rogers, AR, United StatesSpecification developer0000api.fda.gov
Flotec, Inc.Eagle Creek, IN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
ICU Medical, Inc.Dublin, OH, United StatesContract manufacturer0000api.fda.gov
Inovo Inc.Lehigh Acres, FL, United StatesManufacturer0000api.fda.gov
Integra LifeSciences CorporationPrinceton, NJ, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Kmi Imi Group / Dba: Innovative Med, Inc.Irvine, CA, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Life CorporationOrlando, FL, United StatesManufacturer0000api.fda.gov
Lifeport, LLC.Woodland, WA, United StatesManufacturer0000api.fda.gov
Linde Gas & Equipment Inc.Tonawanda, NY, United StatesSpecification developer0000api.fda.gov
Linvatec CorporationLargo, FL, United StatesManufacturer0000api.fda.gov
Mada Medical Products, Inc.Carlstadt, NJ, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Microaire Surgical Instruments LLCCharlottesville, VA, United StatesSpecification developer0000api.fda.gov
Micromedics, Inc.Saint Paul, MN, United StatesManufacturer0000api.fda.gov
Ohio Medical LLCGurnee, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Pmda, LLC.Fort Myers, FL, United StatesManufacturer0000api.fda.gov
Precision Medical, Inc.Northampton, PA, United StatesManufacturer0010api.fda.gov
Spiracle TechnologyLos Alamitos, CA, United StatesManufacturer, Specification developer0000api.fda.gov
Siemens Healthcare Diagnostics IncEast Walpole, MA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Siemens Healthcare Diagnostics Inc.Tarrytown, NY, United StatesSpecification developer0000api.fda.gov
Synthes (USA) Products LLCWest Chester, PA, United StatesSpecification developer0000api.fda.gov
The Harris Products GroupGainesville, GA, United StatesManufacturer0000api.fda.gov
Vapotherm Inc.Exeter, NH, United StatesManufacturer0000api.fda.gov
Western Enterprises, Inc.Westlake, OH, United StatesManufacturer0051api.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.