Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3023140863

FEI Number

3023140863

Entity Name

FIRMTECH INC.

City/State/Country

Bozeman, MT, US

Establishment Address

7446 S. Cottonwood Road, Bozeman, MT 59718, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

FirmTech Inc. (Owner Number: 10084566)

Owner / Operator Contact Address

305 Broadway, 7th FL, New York, NY 10007, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

FirmTech Performance Ring FirmTech Tech Ring

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LKY	Device, External Penile Rigidity	Gastroenterology, Urology	Class 2	876.5020	2022-05-26

Official Correspondent

Rachael Kierych

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

FirmTech Inc.

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 3023140863. Last updated year: 2026. Please use registration number 3023140863 when referencing this establishment in official correspondence.