Data / Medical devices / Connector, Ureteral Catheter

Connector, Ureteral Catheter (EYK): 17 FDA-registered makers in 8 countries

Name: FDA-registered makers of Connector, Ureteral Catheter
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

17 establishments in 8 countries are registered with the FDA to make Connector, Ureteral Catheter (product code EYK, Class 1, 21 CFR 876.5130). 0 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 1 510(k) clearance under this code, the latest on May 25, 1994, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.

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Product code: EYK
Device class: 1
Regulation: 876.5130
Medical specialty: Gastroenterology, Urology

Makers by country

Country	Makers
United States	6
Pakistan	4
China	2
Egypt	1
Costa Rica	1
Poland	1
Turkey	1
Germany	1

Makers of Connector, Ureteral Catheter

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

Maker	Location	Role	Source
Ameco Medical Industries	10TH OF RAMADAN CITY Ash Sharqiyah, Egypt	Contract manufacturer, Exporter to the US, Manufacturer	api.fda.gov
Boston Scientific Corporation	Marlborough, MA, United States	Specification developer	api.fda.gov
Boston Scientific Corporation	Spencer, IN, United States	Manufacturer	api.fda.gov
Boston Scientific Corporation	El Coyol Alajuela, Costa Rica	Manufacturer	api.fda.gov
CALYX MEDICAL Sp. Z.O.O.	Wroclaw Dolnoslaskie, Poland	Specification developer	api.fda.gov
Cook Incorporated	Bloomington, IN, United States	Complaint file establishment, Manufacturer	api.fda.gov
Cook Incorporated	Spencer, IN, United States	Manufacturer	api.fda.gov
Falcon Surgical Co. (Pvt.) Ltd.	Sialkot Punjab, Pakistan	Manufacturer	api.fda.gov
Hexamed Pvt Ltd	Sialkot Punjab, Pakistan	Contract manufacturer, Manufacturer	api.fda.gov
Hilbro International (pvt) Limited	SIALKOT Punjab, Pakistan	Contract manufacturer, Manufacturer	api.fda.gov
Huzhou Junda Industry Co., Ltd.	Anji Zhejiang, China	Contract manufacturer, Exporter to the US, Manufacturer	api.fda.gov
Jiangsu Hanheng Medical Technology Co., Ltd	Changzhou Jiangsu, China	Manufacturer	api.fda.gov
Mecmed Medical	Sialkot Punjab, Pakistan	Manufacturer	api.fda.gov
Plasti-Med Plastik Medikal Urunler San. Ve Tic. Ltd. Sti.	Tuzla Istanbul, Turkey	Exporter to the US, Manufacturer	api.fda.gov
RZ Medizintechnik GMBH	TUTTLINGEN Baden-Wurttemberg, Germany	Manufacturer	api.fda.gov
Teleflex Medical LLC	Morrisville, NC, United States	Complaint file establishment, Specification developer	api.fda.gov
VLV Associates, Inc.	Whippany, NJ, United States	Contract manufacturer	api.fda.gov

Updated May 25, 1994. 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.