Oktas
Country not established
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Video Endoscope System With Zoom Ref K946171
Regimes: 510(k) Registry: 510(k)3 Dimensional Video Endoscope Ref K970214
Regimes: 510(k) Registry: 510(k)Oktas Endoscopy Video Camera System Ref K941919
Regimes: 510(k) Registry: 510(k)Oktas Stereo Viewing System Ref K944254
Regimes: 510(k) Registry: 510(k)3D Scope Ref K961182
Regimes: 510(k) Registry: 510(k)Vista Mini Camera System Ref K970369
Regimes: 510(k) Registry: 510(k)Oktas Intra-Oral Dental Camera Ref K944256
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Oktas have in the registry?
The registry currently lists 7 devices for Oktas. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oktas's devices?
Among its 7 most recently registered devices, Oktas has devices listed in FDA 510(k) (7 devices).
What risk classes do Oktas's devices fall under?
Among its 7 most recently registered devices, the classes recorded for Oktas's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oktas in the registry?
The most recently registered devices listed for Oktas include VIDEO ENDOSCOPE SYSTEM WITH ZOOM, 3 DIMENSIONAL VIDEO ENDOSCOPE, OKTAS ENDOSCOPY VIDEO CAMERA SYSTEM and OKTAS STEREO VIEWING SYSTEM.