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Data / Medical devices / Bandage, Liquid, Skin Protectant / United States

FDA-registered makers of Bandage, Liquid, Skin Protectant in the United States: 19 establishments

19 establishments in the United States are registered with the FDA to make Bandage, Liquid, Skin Protectant (product code NEC). 0 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
Bandage, Liquid, Skin Protectant
Product code
NEC
Country
United States

Makers of Bandage, Liquid, Skin Protectant in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
3M CompanySaint Paul, MN, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Advantice Health, LLCBridgewater, NJ, United StatesComplaint file establishment, Specification developer0000api.fda.gov
American Spraytech, L.L.C.Branchburg, NJ, United StatesContract manufacturer0000api.fda.gov
Aphena Pharma Solutions - Maryland, LLCEaston, MD, United StatesContract manufacturer0000api.fda.gov
C.R. Bard, Inc.Covington, GA, United StatesSpecification developer0000api.fda.gov
Chemence Medical Inc.Alpharetta, GA, United StatesContract manufacturer0000api.fda.gov
Chemence Medical Inc.Alpharetta, GA, United StatesContract manufacturer, Specification developer0000api.fda.gov
Epien Medical, Inc.White Bear Lake, MN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
HK Kolmar Usa, LLCOlyphant, PA, United StatesContract manufacturer, Manufacturer, Specification developer0000api.fda.gov
Hollister IncorporatedLibertyville, IL, United StatesSpecification developer0000api.fda.gov
Kericure MedicalLand O Lakes, FL, United StatesSpecification developer0000api.fda.gov
Liquidpro UsSanta Rosa, CA, United StatesManufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesComplaint file establishment, Specification developer0010api.fda.gov
Mueller Sports Medicine, Inc.Prairie Du Sac, WI, United StatesComplaint file establishment, Manufacturer, Repackager or relabeler, Specification developer0000api.fda.gov
Medline Industries, LPNorth Mankato, MN, United StatesContract manufacturer0000api.fda.gov
Nitro Quimica CorporationCollege Park, GA, United StatesManufacturer0000api.fda.gov
Safe N Simple LLCClarkston, MI, United StatesManufacturer0010api.fda.gov
SPAN PACKAGING SERVICES d.b.a. MULTI-PACK SOLUTIONSGreenville, SC, United StatesContract manufacturer0000api.fda.gov
Swiss-American CDMO,LLCCarrollton, TX, United StatesContract 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.