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Data / Medical devices / Bandage, Liquid / United States

FDA-registered makers of Bandage, Liquid in the United States: 23 establishments

23 establishments in the United States are registered with the FDA to make Bandage, Liquid (product code KMF). 16 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.

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Device
Bandage, Liquid
Product code
KMF
Country
United States

Makers of Bandage, Liquid in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Cardinal HealthHazelwood, MO, United StatesSpecification developer4December 10, 1997000api.fda.gov
Cardinal HealthAugusta, GA, United StatesManufacturer4December 10, 1997000api.fda.gov
Ferris MFG. Corp.Fort Worth, TX, United StatesManufacturer4August 27, 1999000api.fda.gov
Solventum Us LLCEagan, MN, United StatesSpecification developer3August 23, 2016000api.fda.gov
Solventum US LLCSan Antonio, TX, United StatesComplaint file establishment, Specification developer3August 23, 2016000api.fda.gov
Chemence Medical Inc.Alpharetta, GA, United StatesManufacturer2June 19, 2006000api.fda.gov
Marine Polymer Technologies, Inc.Topsfield, MA, United StatesManufacturer2October 14, 2008000api.fda.gov
Solventum US LLCColumbia, MO, United StatesManufacturer2August 23, 2016000api.fda.gov
Aleo Bme Inc. MRMState College, PA, United StatesManufacturer1January 12, 2018000api.fda.gov
H.B. Fuller Medical Adhesive Technologies, LLCHudson, NC, United StatesManufacturer1May 2, 2007000api.fda.gov
Kericure MedicalLand O Lakes, FL, United StatesSpecification developer1August 7, 2014000api.fda.gov
Novabay Pharmaceuticals, IncEmeryville, CA, United StatesManufacturer1May 20, 2008000api.fda.gov
OptMed, IncNew York, NY, United StatesComplaint file establishment, Specification developer1September 27, 2024000api.fda.gov
Prevent Plus, LLC.Saint Louis, MO, United StatesSpecification developer1June 25, 2004000api.fda.gov
Rochal Technologies LLCSan Antonio, TX, United StatesSpecification developer1July 26, 2016000api.fda.gov
Solventum US LLCBrookings, SD, United StatesManufacturer1February 5, 1996000api.fda.gov
Aphena Pharma Solutions - Maryland, LLCEaston, MD, United StatesContract manufacturer0000api.fda.gov
Chemence Medical Inc.Alpharetta, GA, United StatesContract manufacturer0000api.fda.gov
DPT Laboratories, Ltd.San Antonio, TX, United StatesContract manufacturer0000api.fda.gov
James Alexander Corp.Blairstown, NJ, United StatesContract manufacturer0000api.fda.gov
SPAN PACKAGING SERVICES d.b.a. MULTI-PACK SOLUTIONSGreenville, SC, United StatesContract manufacturer0000api.fda.gov
Summit Medical LLCSaint Paul, MN, United StatesManufacturer for export0000api.fda.gov
Swiss-American CDMO,LLCCarrollton, TX, United StatesContract manufacturer0000api.fda.gov

Updated November 3, 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.