Endosec Corporation
Country not established
- Devices
- 1
What Endosec Corporation makes
Endosec Corporation manufactures the U-SCOPE 8000 System with HSC+EMB Cannula, a device designed for endoscopic procedures, combining high-definition imaging and specialized cannula technology for internal diagnostic and therapeutic applications.
The U-SCOPE 8000 System with HSC+EMB Cannula is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
U-Scope 8000 System With Hsc+emb Cannula Ref K132384
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endosec Corporation have in the registry?
The registry currently lists 1 device for Endosec Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endosec Corporation's devices?
Among its 1 most recently registered device, Endosec Corporation has devices listed in FDA 510(k) (1 device).
What risk classes do Endosec Corporation's devices fall under?
Among its 1 most recently registered device, the classes recorded for Endosec Corporation's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endosec Corporation in the registry?
The most recently registered devices listed for Endosec Corporation include U-SCOPE 8000 SYSTEM WITH HSC+EMB CANNULA.