Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030154790

FEI Number

3030154790

Entity Name

HIRSH PRECISION PRODUCTS

City/State/Country

Frederick, CO, US

Establishment Address

4300 Godding Hollow Parkway, Frederick, CO 80504, US

Establishment Type(s)

Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Hirsh Precision Products (Owner Number: 10089561)

Owner / Operator Contact Address

4300 Godding Hollow Parkway, Frederick, CO 80504, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PRO-W-T Tapered Wire Probe, Ball End

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HXB	Probe	Orthopedic	Class 1	888.4540	2023-12-18

Official Correspondent

Annette Siverling

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Hirsh Precision Products

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

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030154790. Last updated year: 2026. Please use registration number 3030154790 when referencing this establishment in official correspondence.