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Data / Medical devices / Collector, Urine, (And Accessories) For Indwelling Catheter / United States

FDA-registered makers of Collector, Urine, (And Accessories) For Indwelling Catheter in the United States: 18 establishments

18 establishments in the United States are registered with the FDA to make Collector, Urine, (And Accessories) For Indwelling Catheter (product code KNX). 4 have a 510(k) clearance or PMA approval on file and 3 have a recall event. FDA data exported November 3, 2026.

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Device
Collector, Urine, (And Accessories) For Indwelling Catheter
Product code
KNX
Country
United States

Makers of Collector, Urine, (And Accessories) For Indwelling Catheter in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Customed, Inc.Fajardo, PR, United StatesManufacturer, Repackager or relabeler2August 6, 1997010api.fda.gov
Deroyal Industries, Inc.Powell, TN, United StatesComplaint file establishment, Specification developer1February 12, 1982000api.fda.gov
Deroyal Industries, Inc.New Tazewell, TN, United StatesContract manufacturer, Repackager or relabeler1February 12, 1982000api.fda.gov
Teleflex Medical LLCMorrisville, NC, United StatesComplaint file establishment, Specification developer1May 29, 1987020api.fda.gov
Bard Shannon LimitedHumacao, PR, United StatesContract manufacturer0000api.fda.gov
Busse Hospital DisposablesHauppauge, NY, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
C.R. Bard, Inc.Covington, GA, United StatesComplaint file establishment, Contract sterilizer, Manufacturer, Specification developer0050api.fda.gov
Compactcath, IncPalo Alto, CA, United StatesSpecification developer0000api.fda.gov
Cardinal HealthHazelwood, MO, United StatesSpecification developer0000api.fda.gov
Demetech Corp.Miami Lakes, FL, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Eagle Electrode Manufacturing, LLCIjamsville, MD, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Greystone Medical, LLCWaterford, MI, United StatesSpecification developer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Mendtronix, Inc.San Diego, CA, United StatesContract manufacturer, Repackager or relabeler0000api.fda.gov
Medegen Medical ProductsGallaway, TN, United StatesSpecification developer0000api.fda.gov
Multiphze, LLCLos Angeles, CA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
NBS Group Supply- Medical Products Division, LLCNew Brunswick, NJ, United StatesSpecification developer0000api.fda.gov
Urocare Products, Inc.Pomona, CA, United StatesManufacturer0000api.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.