Arthex, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Arthex, Inc. makes
Arthex, Inc. makes the FiberTak DX, a suture anchor device used for soft tissue fixation in orthopedic procedures. They also produce the Arthrex SynergyID Endoscopic Imaging System, which provides visualization during minimally invasive surgery, and the Arthrex BioSync® Bone Wedge, an implant used for bone grafting and joint stabilization.
These devices are classified as Class II medical devices and are listed in the FDA 510(k) premarket notification database. The company is based in the United States.
Catalogue
FiberTak DX Ref K172612
Regimes: 510(k) Registry: 510(k)Arthrex SynergyID Endoscopic Imaging System Ref K223759
Regimes: 510(k) Registry: 510(k)Arthrex BioSync® Bone Wedge Ref K151256
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arthex, Inc. have in the registry?
The registry currently lists 3 devices for Arthex, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arthex, Inc.'s devices?
Among its 3 most recently registered devices, Arthex, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Arthex, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Arthex, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arthex, Inc. in the registry?
The most recently registered devices listed for Arthex, Inc. include FiberTak DX, Arthrex SynergyID Endoscopic Imaging System and Arthrex BioSync® Bone Wedge.