Data / Medical devices / United States / ArthroTAK, LLC

ArthroTAK, LLC: FDA-registered device maker in Missoula, MT, United States, 1 510(k) clearance

ArthroTAK, LLC is registered with the FDA (registration 3045178691) in Missoula, MT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated May 1, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number

3045178691

Address

2925 Stockyard Rd Suite B, Missoula, MT, United States, 59808

Owner or operator

ArthroTAK (10095824)

Roles

Complaint file establishment, Specification developer

First device listed

May 5, 2026

Registered through

2026

Brand names listed

ArthroTAK Tendon Anchor Kit

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Compare with other makers

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Updated May 1, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.