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Data / Medical devices / Holder, Ureteral Catheter / United States

FDA-registered makers of Holder, Ureteral Catheter in the United States: 21 establishments

21 establishments in the United States are registered with the FDA to make Holder, Ureteral Catheter (product code EYJ). 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
Holder, Ureteral Catheter
Product code
EYJ
Country
United States

Makers of Holder, Ureteral Catheter in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Alera Medtech LLCBuckley, WA, United StatesComplaint file establishment, Manufacturer, Specification developer0000api.fda.gov
American I.V. Products, Inc.Harmans, MD, United StatesManufacturer0000api.fda.gov
Beauxregard IndustriesSarasota, FL, United StatesSpecification developer0000api.fda.gov
Bird & Cronin, LLCEagan, MN, United StatesContract manufacturer, Manufacturer0000api.fda.gov
C.R. Bard, Inc.Covington, GA, United StatesSpecification developer0000api.fda.gov
Carwild Corp.New London, CT, United StatesContract manufacturer0000api.fda.gov
Centurion Medical Products, LPHowell, MI, United StatesManufacturer, Repackager or relabeler0000api.fda.gov
Cook IncorporatedBloomington, IN, United StatesComplaint file establishment, Manufacturer0000api.fda.gov
Cook IncorporatedSpencer, IN, United StatesManufacturer0000api.fda.gov
Dale Medical Products, Inc.New London, CT, United StatesManufacturer0000api.fda.gov
FabriteqKnoxville, TN, United StatesContract manufacturer0000api.fda.gov
HR PHARMACEUTICALS, INC d/b/a HR HealthCareYork, PA, United StatesComplaint file establishment, Specification developer0000api.fda.gov
Invomed LLCVancouver, WA, United StatesSpecification developer0000api.fda.gov
M & C Specialties Co.Southampton, PA, United StatesContract manufacturer0000api.fda.gov
M. C. Johnson Co., Inc.Ft Myers, FL, United StatesSpecification developer0000api.fda.gov
Marble Medical, Inc.Tallahassee, FL, United StatesContract manufacturer0000api.fda.gov
MEDLINE INDUSTRIES, LP - NorthfieldNorthfield, IL, United StatesSpecification developer0000api.fda.gov
Pepper Medical, Inc.West Chester, PA, United StatesRepackager or relabeler, Specification developer0000api.fda.gov
Prestige AmeritechNorth Richland Hills, TX, United StatesContract manufacturer, Manufacturer0000api.fda.gov
Tidi Products, LLCNeenah, WI, United StatesContract manufacturer, Manufacturer0000api.fda.gov
TZ Medical, Inc.Tualatin, OR, 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.