Ti-Mesh, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Ti-Mesh, Inc. makes
Ti-Mesh, Inc. manufactures titanium-based orthopedic implants, including the TIMESH Titanium Mini-SoftPlate/Screw for bone fixation, the Tilghman Titanium Mesh Skeletal Orbit Liner for orbital reconstruction, and the TISMESH System for soft tissue reinforcement.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Timesh Titanium Mini-Softplate/Screw Ref K923802
Regimes: 510(k) Registry: 510(k)Tilghman Titanium Mesh Skeletal Orbit Liner Ref K922308
Regimes: 510(k) Registry: 510(k)Tismesh System Ref K923419
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ti-Mesh, Inc. have in the registry?
The registry currently lists 3 devices for Ti-Mesh, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ti-Mesh, Inc.'s devices?
Among its 3 most recently registered devices, Ti-Mesh, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Ti-Mesh, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Ti-Mesh, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ti-Mesh, Inc. in the registry?
The most recently registered devices listed for Ti-Mesh, Inc. include TIMESH TITANIUM MINI-SOFTPLATE/SCREW, TILGHMAN TITANIUM MESH SKELETAL ORBIT LINER and TISMESH SYSTEM.