Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007856226

FEI Number

3007856226

Entity Name

BROWN PRECISION INC

City/State/Country

Huntsville, AL, US

Establishment Address

90 Shields Rd, Huntsville, AL 35811, US

Establishment Type(s)

Manufacture Medical Device,Reprocess Single-Use Device

Owner / Operator

Brown Precision Inc (Owner Number: 10057558)

Owner / Operator Contact Address

90 Shields Rd, Huntsville, AL 35811, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K081111

PMA Number

N/A

All Registered Proprietary Names

Bone Plates

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KRO	Prosthesis, Knee, Femorotibial, Constrained, Cemented, Metal/Polymer	Orthopedic	Class 2	888.3510	2018-04-24

Official Correspondent

Patricia Reagan

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Brown Precision 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
K220628	Waldemar Link GmbH & Co. KG	LINK Endo-Model EVO Knee System	2022-05-03

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007856226. Last updated year: 2026. Please use registration number 3007856226 when referencing this establishment in official correspondence.