Carbofix Orthpedics, Ltd.
IsraelFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
CarboClear Lumbar Cage System Ref K203683
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Carbofix Orthpedics, Ltd. have in the registry?
The registry currently lists 2 devices for Carbofix Orthpedics, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Carbofix Orthpedics, Ltd.'s devices?
Among its 2 most recently registered devices, Carbofix Orthpedics, Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Carbofix Orthpedics, Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Carbofix Orthpedics, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Carbofix Orthpedics, Ltd. in the registry?
The most recently registered devices listed for Carbofix Orthpedics, Ltd. include CarboClear Cervical Cage System, CarboClear Cervical VBR System and CarboClear Lumbar Cage System.