CarboFix Orhtopedics, Ltd.
IsraelFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
CarboClear® Cervical Navigated Instruments Ref K263154
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does CarboFix Orhtopedics, Ltd. have in the registry?
The registry currently lists 1 device for CarboFix Orhtopedics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list CarboFix Orhtopedics, Ltd.'s devices?
Among its 1 most recently registered device, CarboFix Orhtopedics, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do CarboFix Orhtopedics, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for CarboFix Orhtopedics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from CarboFix Orhtopedics, Ltd. in the registry?
The most recently registered devices listed for CarboFix Orhtopedics, Ltd. include CarboClear® Cervical Navigated Instruments.