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Data / Medical devices / Cannula, Nasal, Oxygen / United States

FDA-registered makers of Cannula, Nasal, Oxygen in the United States: 34 establishments

34 establishments in the United States are registered with the FDA to make Cannula, Nasal, Oxygen (product code CAT). 1 has 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
Cannula, Nasal, Oxygen
Product code
CAT
Country
United States

Makers of Cannula, Nasal, Oxygen in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Salter LabsEl Paso, TX, United StatesSpecification developer3October 18, 1991000api.fda.gov
AG Industries LLCFairburn, GA, United StatesManufacturer0000api.fda.gov
Airway Innovations, Inc.Buffalo Grove, IL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
All Quality & Services, Inc.Garland, TX, United StatesContract manufacturer0000api.fda.gov
Allied Medical LLCEarth City, MO, United StatesManufacturer, Specification developer0000api.fda.gov
Barbaras Development, Inc.Thousand Oaks, CA, United StatesContract manufacturer0000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Bound Tree Medical, LLCGrand Prairie, TX, United StatesManufacturer0000api.fda.gov
Bausch & Lomb IncorporatedManchester, MO, United StatesManufacturer0000api.fda.gov
Draeger Medical Systems, Inc.Andover, MA, United StatesManufacturer0000api.fda.gov
Doner Industries, Inc.Rogers, AR, United StatesSpecification developer0000api.fda.gov
DynastheticsSalt Lake City, UT, United StatesManufacturer0000api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Invent Medical CorporationCarlsbad, CA, United StatesSpecification developer0000api.fda.gov
Inventeur, LLCSaint Petersburg, FL, United StatesSpecification developer0000api.fda.gov
Life CorporationOrlando, FL, United StatesManufacturer0000api.fda.gov
Loewenstein Medical Americas Corp.Alpharetta, GA, United StatesSpecification developer0000api.fda.gov
Mada Medical Products, Inc.Carlstadt, NJ, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Masimo CorporationIrvine, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Med-Linket CorpAlhambra, CA, United StatesManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Neotech Products, LLCValencia, CA, United StatesManufacturer, Specification developer0000api.fda.gov
Neurovirtual Usa, Inc.Fort Lauderdale, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Plastics Plus Technology, Inc.Redlands, CA, United StatesContract manufacturer0000api.fda.gov
Respironics Novametrix, LLCAndover, MA, United StatesSpecification developer0000api.fda.gov
SMC Ltd.Devens, MA, United StatesContract manufacturer0000api.fda.gov
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesSpecification developer0000api.fda.gov
Sunset Healthcare Solutions Central WarehouseElgin, IL, United StatesRemanufacturer0000api.fda.gov
Tidi Products, LLCNeenah, WI, United StatesManufacturer0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer0010api.fda.gov
Telesair, Inc.Irvine, CA, United StatesManufacturer0000api.fda.gov
Trelleborg Sealing Solutions US, IncDelano, MN, United StatesContract manufacturer0000api.fda.gov
Vapotherm Inc.Exeter, NH, United StatesSpecification developer0000api.fda.gov
Westmed, Inc.Tucson, AZ, United StatesContract manufacturer, Manufacturer, Repackager or relabeler, Specification developer0000api.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.