Endosee Corp
Country not established
- Devices
- 1
What Endosee Corp makes
Endosee Corp manufactures the Endosee Model 8000 U-Scope, a device designed for endoscopic imaging and visualization within the gastrointestinal tract. This system is intended to assist in the detection and examination of internal structures, including mucosal surfaces and abnormalities.
The Endosee Model 8000 U-Scope is classified as a Class II medical device in the US and has been submitted for 510(k) clearance through the FDA regulatory pathway. The company is based in the United States.
Catalogue
Endosee Model 8000 U-Scope Ref K123151
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endosee Corp have in the registry?
The registry currently lists 1 device for Endosee Corp. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endosee Corp's devices?
Among its 1 most recently registered device, Endosee Corp has devices listed in FDA 510(k) (1 device).
What risk classes do Endosee Corp's devices fall under?
Among its 1 most recently registered device, the classes recorded for Endosee Corp's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endosee Corp in the registry?
The most recently registered devices listed for Endosee Corp include ENDOSEE MODEL 8000 U-SCOPE.