Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011446173

FEI Number

3011446173

Entity Name

FISCHER MANUFACTURING LLC

City/State/Country

Fairfield, OH, US

Establishment Address

2052 Bohlke Blvd, Fairfield, OH 45014, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Fischer Manufacturing LLC (Owner Number: 10048572)

Owner / Operator Contact Address

2052 Bohlke Blvd, Fairfield, OH 45014, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2016-07-11
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2017-12-22

Official Correspondent

Albert Fischer

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Fischer Manufacturing 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
K823241	Kimberly-Clark Corp.	NEW FREEDOM THIN UNSCENTED MAXI PADS	1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011446173. Last updated year: 2026. Please use registration number 3011446173 when referencing this establishment in official correspondence.