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Data / Medical devices / Foley Catheter Kit (Excludes Hiv Testing) / United States

FDA-registered makers of Foley Catheter Kit (Excludes Hiv Testing) in the United States: 6 establishments

6 establishments in the United States are registered with the FDA to make Foley Catheter Kit (Excludes Hiv Testing) (product code PPB). 0 have 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
Foley Catheter Kit (Excludes Hiv Testing)
Product code
PPB
Country
United States

Makers of Foley Catheter Kit (Excludes Hiv Testing) in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Cardinal Health 200, LLCEl Paso, TX, United StatesManufacturer0000api.fda.gov
Deroyal Industries, Inc.New Tazewell, TN, United StatesContract manufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - LaredoLaredo, TX, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Medline Industries, LP - SPTWaukegan, IL, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
North American Rescue, LLC.Greer, SC, 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.