Tarsus Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Tarsus Medical, Inc. makes
Tarsus Medical, Inc. manufactures orthopedic repair kits, including the SYNDE-LOCK Synдесmosis Repair Kit for ligamentous joint stabilization and the META-LOCK Suture Anchor System for securing soft tissues to bone. These products are designed for surgical applications in trauma and sports medicine procedures.
The company’s devices are classified as Class II under FDA regulations and are authorised through the 510(k) clearance process. The portfolio is listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Synde-Lock Syndesmosis Repair Kit Ref K111971
Regimes: 510(k) Registry: 510(k)Meta-Lock Suture Anchor System Ref K110800
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tarsus Medical, Inc. have in the registry?
The registry currently lists 2 devices for Tarsus Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tarsus Medical, Inc.'s devices?
Among its 2 most recently registered devices, Tarsus Medical, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Tarsus Medical, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Tarsus Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Tarsus Medical, Inc. in the registry?
The most recently registered devices listed for Tarsus Medical, Inc. include SYNDE-LOCK SYNDESMOSIS REPAIR KIT and META-LOCK SUTURE ANCHOR SYSTEM.