Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042641002

FEI Number

3042641002

Entity Name

PEAX EQUIPMENT CO. LLC

City/State/Country

Bozeman, MT, US

Establishment Address

96 Laura Louise Ln, Ste 17, Bozeman, MT 59718, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Peax Equipment Co. LLC (Owner Number: 10094507)

Owner / Operator Contact Address

96 Laura Louise Ln, Ste 17, Bozeman, MT 59718, 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
LRR	First Aid Kit With Drug	Unknown	Class N	N/A	2025-12-04

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Peax Equipment Co. LLC

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 3042641002. Last updated year: 2026. Please use registration number 3042641002 when referencing this establishment in official correspondence.