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Data / Medical devices / Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use / United States

FDA-registered makers of Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use in the United States: 14 establishments

14 establishments in the United States are registered with the FDA to make Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use (product code PYO). 0 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
Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use
Product code
PYO
Country
United States

Makers of Tape And Bandage, Adhesive, Adjustable Closing Mechanism, Otc Use in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
A-1 Creative Packaging LLCFort Atkinson, WI, United StatesContract manufacturer0000api.fda.gov
Alimed, LLCDedham, MA, United StatesManufacturer0000api.fda.gov
Applied Medical Technology, Inc.Brecksville, OH, United StatesManufacturer0000api.fda.gov
Avanos Medical, Inc.Alpharetta, GA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Cordica Medical, Inc.Haverhill, MA, United StatesContract manufacturer0000api.fda.gov
Dermaclip Us, LLCHouston, TX, United StatesSpecification developer0000api.fda.gov
Duct-AidCedar City, UT, United StatesManufacturer, Specification developer0000api.fda.gov
Karl Storz Imaging, Inc.Goleta, CA, United StatesContract manufacturer0000api.fda.gov
M & C Specialties Co.Southampton, PA, United StatesContract manufacturer0000api.fda.gov
Onlycare IncDenver, CO, United StatesManufacturer0000api.fda.gov
Pharmchem, Inc.Fort Worth, TX, United StatesSpecification developer0000api.fda.gov
Simple Style IncBrighton, CO, United StatesSpecification developer0000api.fda.gov
The Marena Group, LLC.Lawrenceville, GA, United StatesManufacturer0000api.fda.gov
TNT Moborg Intl. Ltd.Williamsville, NY, United StatesSpecification developer0000api.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.