Endoscopy Division
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endoscopy Division have in the registry?
The registry currently lists 1 device for Endoscopy Division. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endoscopy Division's devices?
Among its 1 most recently registered device, Endoscopy Division has devices listed in FDA 510(k) (1 device).
What risk classes do Endoscopy Division's devices fall under?
Among its 1 most recently registered device, the classes recorded for Endoscopy Division's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endoscopy Division in the registry?
The most recently registered devices listed for Endoscopy Division include SMITH & NEPHEW DYONICS ARTHOSCOPES/ENDOSCOPES, SMITH & NEPHEW DYONICS LAPAROSCOPES, SNITH & NEPHEW DYONICS HYSTEROSCOPES.