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Data / Medical devices / Irrigator, Powered Nasal / United States

FDA-registered makers of Irrigator, Powered Nasal in the United States: 8 establishments

8 establishments in the United States are registered with the FDA to make Irrigator, Powered Nasal (product code KMA). 1 has a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.

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Device
Irrigator, Powered Nasal
Product code
KMA
Country
United States

Makers of Irrigator, Powered Nasal in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Rhinosystems, Inc.Brooklyn, OH, United StatesSpecification developer1June 27, 2014000api.fda.gov
Drmenta,incAlbany, NY, United StatesContract manufacturer, Manufacturer for export0000api.fda.gov
Health Solutions Medical Products, Corp.Los Angeles, CA, United StatesSpecification developer0000api.fda.gov
Kaz USA, Inc., A Helen of Troy CompanyMarlborough, MA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Medtronic Xomed, Inc.Jacksonville, FL, United StatesManufacturer0000api.fda.gov
Michael Todd Beauty, LPPort St Lucie, FL, United StatesSpecification developer0000api.fda.gov
Neilmed Pharmaceuticals, Inc.Santa Rosa, CA, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Tesla Biohealing, Inc.Milford, DE, 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.