Synovis Orthopedic & Woundcare
Also registered as Synovis Orthopedic and Woundcare, Inc.
Country not established
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Proseries Bioimplants-Proankle/Procuff Ref K112786
Regimes: 510(k) Registry: 510(k)Unite Biomatrix Ref K112399
Regimes: 510(k) Registry: 510(k)Synergy Tissue Matrix Ref K113460
Regimes: 510(k) Registry: 510(k)Pro Fixation System Ref K110538
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Synovis Orthopedic & Woundcare have in the registry?
The registry currently lists 4 devices for Synovis Orthopedic & Woundcare. Devices recorded under merged duplicate company entries are counted once.
Which registries list Synovis Orthopedic & Woundcare's devices?
Among its 4 most recently registered devices, Synovis Orthopedic & Woundcare has devices listed in FDA 510(k) (4 devices).
What risk classes do Synovis Orthopedic & Woundcare's devices fall under?
Among its 4 most recently registered devices, the classes recorded for Synovis Orthopedic & Woundcare's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Synovis Orthopedic & Woundcare in the registry?
The most recently registered devices listed for Synovis Orthopedic & Woundcare include PROSERIES BIOIMPLANTS-PROANKLE/PROCUFF, UNITE BIOMATRIX, SYNERGY TISSUE MATRIX and PRO FIXATION SYSTEM.