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Data / Medical devices / Airway, Oropharyngeal, Anesthesiology / United States

FDA-registered makers of Airway, Oropharyngeal, Anesthesiology in the United States: 31 establishments

31 establishments in the United States are registered with the FDA to make Airway, Oropharyngeal, Anesthesiology (product code CAE). 3 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.

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Device
Airway, Oropharyngeal, Anesthesiology
Product code
CAE
Country
United States

Makers of Airway, Oropharyngeal, Anesthesiology in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Allied Medical LLCEarth City, MO, United StatesSpecification developer1April 9, 1986000api.fda.gov
King Systems Corporation.Noblesville, IN, United StatesRepackager or relabeler, Specification developer1April 14, 2004090api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer1May 30, 2014010api.fda.gov
Airguard LLCFairfield, CT, United StatesSpecification developer0000api.fda.gov
Airway Innovations, Inc.Buffalo Grove, IL, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Arete Medical DevicesMullica Hill, NJ, United StatesManufacturer0000api.fda.gov
Anesthesia Associates, Inc.San Marcos, CA, United StatesManufacturer, Repackager or relabeler0000api.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
CovidienLafayette, CO, United StatesSpecification developer0000api.fda.gov
Doner Industries, Inc.Rogers, AR, United StatesSpecification developer0000api.fda.gov
Endure Industries, Inc.Homer, NY, United StatesManufacturer0000api.fda.gov
Gardner Medical Instruments, LLCFrankfort, IL, United StatesSpecification developer0000api.fda.gov
Icu Medical, Inc.San Clemente, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Made, University Of IowaIowa City, IA, United StatesManufacturer0000api.fda.gov
Mcmurray MedicalMinneapolis, MN, United StatesSpecification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0041api.fda.gov
MedSource Labs, LLCChanhassen, MN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Mercury Medical Enterprises, LLCClearwater, FL, United StatesManufacturer0000api.fda.gov
Microtek Medical LLCEagan, MN, United StatesSpecification developer0000api.fda.gov
Nasorcap Medical, Inc.Venetia, PA, United StatesManufacturer0000api.fda.gov
Ony Biotech Inc.Amherst, NY, United StatesManufacturer0000api.fda.gov
Respironics Inc.Murrysville, PA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Salter LabsEl Paso, TX, United StatesComplaint file establishment, Specification developer0000api.fda.gov
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0010api.fda.gov
The Lethean Company, LLCChester Sprgs, PA, United StatesManufacturer0000api.fda.gov
Tender CorporationLittleton, NH, United StatesComplaint file establishment, Repackager or relabeler, Specification developer0000api.fda.gov
Westmed, Inc.Tucson, AZ, United StatesContract manufacturer, Manufacturer0000api.fda.gov
WM&DGNorthbrook, IL, United StatesManufacturer, Specification developer0000api.fda.gov
Xponent Healthcare IncHudson, MA, United StatesManufacturer0000api.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.