Cit Ortho
Country not established
Cit Ortho is a medical device manufacturer, with 9 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 14 Nov 2026.
- Devices
- 9
Registry facts
- Registries
- FDA GUDID 8
- FDA 510(k) 1
- Device classes
- FDA Class II 9
Catalogue
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Regimes: 510(k) Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Registry: GUDID
- Regimes: 510(k) Registry: GUDID
C Scope Visualization System Ref K203526
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cit Ortho have in the registry?
The registry currently lists 9 devices for Cit Ortho. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cit Ortho's devices?
Among its 9 most recently registered devices, Cit Ortho has devices listed in FDA 510(k) (1 device) and FDA GUDID (8 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Cit Ortho's devices fall under?
Among its 9 most recently registered devices, the classes recorded for Cit Ortho's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cit Ortho in the registry?
The most recently registered devices listed for Cit Ortho include CIT Ortho 613034708, CIT Ortho 613034701, CIT Ortho 613034700 and CIT Ortho 613034705.