# ArthroTAK, LLC

- Location (FDA's records): Missoula, MT
- FDA decisions: 2 (2026–2026): 2 510(k) clearances
- Product codes: MBI (2)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Arthrex, Inc.: 1 (https://510kreport.com/company/arthrex)
- Aevumed, Inc.: 1 (https://510kreport.com/company/aevumed)
- Biomet Manufacturing Corp: 1 (https://510kreport.com/company/biomet-manufacturing)

## Its most-cited devices
- K252635: ArthroTAK Tendon Anchor Kit (2026), cited by 1

## Recent decisions
- K262809: ArthroTAK Tendon Anchor Kit (Sep 2, 2026)
- K252635: ArthroTAK Tendon Anchor Kit (May 1, 2026)

Source page: https://510kreport.com/company/arthrotak