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Data / Medical devices / Ear Wick / United States

FDA-registered makers of Ear Wick in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Ear Wick (product code KCN). 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
Ear Wick
Product code
KCN
Country
United States

Makers of Ear Wick in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Beaver-Visitec International, Inc.Waltham, MA, United StatesSpecification developer1February 1, 1993000api.fda.gov
BiosealPlacentia, CA, United StatesContract manufacturer, Manufacturer, Repackager or relabeler0000api.fda.gov
Carwild Corp.New London, CT, United StatesContract manufacturer, Specification developer0000api.fda.gov
Endure Industries, Inc.Homer, NY, United StatesSpecification developer0000api.fda.gov
Hydrofera, LLC.Manchester, CT, United StatesContract manufacturer0000api.fda.gov
Medtronic Xomed, Inc.Mystic, CT, United StatesManufacturer, Manufacturer for export0000api.fda.gov
Summit Medical LLCSaint Paul, MN, United StatesContract manufacturer, Manufacturer0000api.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.