ArthroTAK, LLC
United StatesFDA applicant, unverified FDA FEI 3045178691
- Devices
- 6
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
What ArthroTAK, LLC makes
ArthroTAK, LLC manufactures the ArthroTAK Tendon Anchor Kit, a surgical device designed for tendon reattachment in orthopedic procedures. The kit is intended for use in procedures requiring secure fixation of tendons to bone, commonly in shoulder or ankle repairs.
The company’s product portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
ArthroTAK Tendon Anchor Kit Ref K262809
Regimes: 510(k) Registry: 510(k)ArthroTAK Tendon Anchor Kit Ref K252635
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3045178691
- DUNS number
- 101071471
- Address
- 2925 Stockyard Rd Suite B, Missoula, MT, 59808
- [email protected]
- Phone
- 2606159555
Frequently asked questions
How many devices does ArthroTAK, LLC have in the registry?
The registry currently lists 6 devices for ArthroTAK, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list ArthroTAK, LLC's devices?
Among its 6 most recently registered devices, ArthroTAK, LLC has devices listed in FDA 510(k) (2 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ArthroTAK, LLC's devices fall under?
Among its 6 most recently registered devices, the classes recorded for ArthroTAK, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ArthroTAK, LLC in the registry?
The most recently registered devices listed for ArthroTAK, LLC include ArthroTAK Tendon Anchor Kit AT-01-100, ArthroTAK Tendon Anchor Kit AT-01-003, ArthroTAK Tendon Anchor Kit AT-01-001 and ArthroTAK Tendon Anchor Kit AT-01-002.