Arthocare Corporation
Country not established
- Devices
- 6
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ambient Turboflash 90 Ifs Ref K120791
Regimes: 510(k) Registry: 510(k)Smartstitch M-Connector Ultra Smartstitch Suture Device Handle Smartstitch Suture Device Handle Ref K121306
Regimes: 510(k) Registry: 510(k)Smartstitch Perfectpasser System Ref K123268
Regimes: 510(k) Registry: 510(k)MultiFIX S Ultra Knotless Fixation System Ref K153669
Regimes: 510(k) Registry: 510(k)Multifix S Knotless Fixation Device Ref K131182
Regimes: 510(k) Registry: 510(k)Endoflip Ref K013334
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Arthocare Corporation have in the registry?
The registry currently lists 6 devices for Arthocare Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Arthocare Corporation's devices?
Among its 6 most recently registered devices, Arthocare Corporation has devices listed in FDA 510(k) (6 devices).
What risk classes do Arthocare Corporation's devices fall under?
Among its 6 most recently registered devices, the classes recorded for Arthocare Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Arthocare Corporation in the registry?
The most recently registered devices listed for Arthocare Corporation include AMBIENT TURBOFLASH 90 IFS, SMARTSTITCH M-CONNECTOR ULTRA SMARTSTITCH SUTURE DEVICE HANDLE SMARTSTITCH SUTURE DEVICE HANDLE, SMARTSTITCH PERFECTPASSER SYSTEM and MultiFIX S Ultra Knotless Fixation System.