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Data / Medical devices / Cover, Barrier, Protective / United States

FDA-registered makers of Cover, Barrier, Protective in the United States: 8 establishments

8 establishments in the United States are registered with the FDA to make Cover, Barrier, Protective (product code MMP). 5 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Cover, Barrier, Protective
Product code
MMP
Country
United States

Makers of Cover, Barrier, Protective in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Aspen Surgical Products, Inc.Caledonia, MI, United StatesManufacturer1September 22, 1997000api.fda.gov
Intl. Medsurg Connection, Inc.Schaumburg, IL, United StatesSpecification developer1February 19, 2002000api.fda.gov
Kerr CorporationPomona, CA, United StatesManufacturer1January 30, 1997000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer1September 22, 2003020api.fda.gov
Petoskey PlasticsPetoskey, MI, United StatesManufacturer1January 30, 1997000api.fda.gov
DeRoyal Industries, Inc.New Tazewell, TN, United StatesContract manufacturer0000api.fda.gov
Pregis Protective Films & CoatingsAurora, IL, United StatesContract manufacturer0000api.fda.gov
Surgentec LLCBoca Raton, FL, 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.