Wright Medical
Country not established
- Devices
- 6
What Wright Medical makes
Wright Medical manufactures orthopedic fixation systems, including the FuseForce Flex Dynamic Compression System for spinal stabilization, the DART-FIRE EDGE Cannulated Screw System for bone fixation, and the SALVATION External Fixation System for limb alignment and stabilization.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company operates from the United States.
Catalogue
FuseForce™ Flex Dynamic Compression System Ref K203832
Regimes: 510(k) Registry: 510(k)Wright Medical Fetasafe Ref K892501
Regimes: 510(k) Registry: 510(k)Wright Pocket Dopplers Vascular & Obstetric Ref K901015
Regimes: 510(k) Registry: 510(k)Baerveldt Glaucoma Implant Ref K905129
Regimes: 510(k) Registry: 510(k)DART-FIRE EDGE Cannulated Screw System Ref K203228
Regimes: 510(k) Registry: 510(k)SALVATION External Fixation System Ref K162033
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Wright Medical have in the registry?
The registry currently lists 6 devices for Wright Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Wright Medical's devices?
Among its 6 most recently registered devices, Wright Medical has devices listed in FDA 510(k) (6 devices).
What risk classes do Wright Medical's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Wright Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Wright Medical in the registry?
The most recently registered devices listed for Wright Medical include FuseForce™ Flex Dynamic Compression System, WRIGHT MEDICAL FETASAFE, WRIGHT POCKET DOPPLERS VASCULAR & OBSTETRIC and BAERVELDT GLAUCOMA IMPLANT.