Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010875172

FEI Number

3010875172

Entity Name

COMMUNITY MEDICAL PRODUCTS LLC

City/State/Country

Prairie du Sac, WI, US

Establishment Address

1510 North St., PO Box 0069, Prairie du Sac, WI 53578, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Community Medical Products, LLC (Owner Number: 10045916)

Owner / Operator Contact Address

1510 North St., PO Box 69, Prairie du Sac, WI 53578, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Squeezer ActiCuf Bright Mirror AstaCath MiWay One Pass Ostomy Draining Device (OPODD)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
FHA	Clamp, Penile	Gastroenterology, Urology	Class 1	876.5160	2021-12-16
ILS	Adaptor, Hygiene	Physical Medicine	Class 1	890.5050	2021-12-16

Official Correspondent

James McHargue

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Community Medical Products, LLC

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
K830425	Maddak, Inc.	TOILET SEAT RAISED	1983-05-09

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010875172. Last updated year: 2026. Please use registration number 3010875172 when referencing this establishment in official correspondence.