Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2023344

FEI Number

2023344

Entity Name

UROCARE PRODUCTS, INC.

City/State/Country

Pomona, CA, US

Establishment Address

2735 MELBOURNE AVE, Pomona, CA 91767, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

UROCARE PRODUCTS INC (Owner Number: 2023344)

Owner / Operator Contact Address

2735 MELBOURNE AVE., Pomona, CA 91767, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

UROCARE URO-SAFE UROCARE UROCARE URO-BOND ADHESIVE REMOVER PADS Uro-Prep UROCARE Tracho-Foam UROCARE UROCARE Urocare

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LZB	Finger Cot	General Hospital	Class 1	880.6250	2007-12-18
FAQ	Bag, Urine Collection, Leg, For External Use, Sterile	Gastroenterology, Urology	Class 1	876.5250	1992-12-03
KOX	Solvent, Adhesive Tape	General, Plastic Surgery	Class 1	878.4730	1992-12-03
EXE	Protector, Ostomy	Gastroenterology, Urology	Class 1	876.5900	2008-08-13
KNX	Collector, Urine, (And Accessories) For Indwelling Catheter	Gastroenterology, Urology	Class 2	876.5250	2018-04-11
EZR	Cement, Stomal Appliance, Ostomy	Gastroenterology, Urology	Class 1	876.5900	2018-06-01
NNW	Bag, Urine Collection, Leg, For External Use, Non-Sterile	Gastroenterology, Urology	Class 1	876.5250	2007-12-18
GCD	Connector, Catheter	General, Plastic Surgery	Class 1	878.4200	2007-12-18
FCN	Urinary Drainage Collection Kit, For Indwelling Catheter	Gastroenterology, Urology	Class 2	876.5250	2018-12-06

Official Correspondent

RAYMOND HALSEY-FRANKE

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

UROCARE PRODUCTS INC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K791969	Medline Industries, Inc.	DYNACOR STERILE CLOSED SYS. DRAINAGE BAG	1979-11-05

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2023344. Last updated year: 2026. Please use registration number 2023344 when referencing this establishment in official correspondence.