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Data / Medical devices / Nebulizer, Medicinal, Non-Ventilatory (Atomizer) / United States

FDA-registered makers of Nebulizer, Medicinal, Non-Ventilatory (Atomizer) in the United States: 19 establishments

19 establishments in the United States are registered with the FDA to make Nebulizer, Medicinal, Non-Ventilatory (Atomizer) (product code CCQ). 5 have 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
Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Product code
CCQ
Country
United States

Makers of Nebulizer, Medicinal, Non-Ventilatory (Atomizer) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
SunMed Group Holdings, LLCGrand Rapids, MI, United StatesComplaint file establishment, Repackager or relabeler, Specification developer2April 1, 1987010api.fda.gov
Alcove Medical, Inc.Cedar City, UT, United StatesManufacturer1September 23, 1997000api.fda.gov
Allied Medical LLCEarth City, MO, United StatesManufacturer1June 9, 1981000api.fda.gov
Monaghan Medical Corp.Plattsburgh, NY, United StatesManufacturer1April 10, 1991000api.fda.gov
Salter LabsEl Paso, TX, United StatesSpecification developer1March 16, 1987000api.fda.gov
Anesthesia Associates, Inc.San Marcos, CA, United StatesManufacturer0000api.fda.gov
B. Braun Us Device Manufacturing LLCAllentown, PA, United StatesContract manufacturer0000api.fda.gov
Bound Tree Medical, LLCGrand Prairie, TX, United StatesManufacturer0000api.fda.gov
DeVilbiss Healthcare LLC.Somerset, PA, United StatesManufacturer0000api.fda.gov
Doner Industries, Inc.Rogers, AR, United StatesSpecification developer0000api.fda.gov
Endocraft LLC.Newton, MA, United StatesManufacturer0000api.fda.gov
Fainteer LimitedLittleton, CO, United StatesManufacturer, Manufacturer for export0000api.fda.gov
Groman Inc.Coconut Creek, FL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Intersurgical Inc.Indianapolis, IN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Mastel Surgical Inc.Schiller Park, IL, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Rhinosystems, Inc.Brooklyn, OH, United StatesSpecification developer0000api.fda.gov
Talbot's Pharmaceuticals Family Products LLCMonroe, LA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer0010api.fda.gov
Westmed, Inc.Tucson, AZ, United StatesContract manufacturer, Manufacturer, 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.