Endo Surgical Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Endo Surgical Devices, Inc. makes
Endo Surgical Devices, Inc. manufactures carbodissecting endoscopes, which are used for minimally invasive surgical procedures to separate and remove tissue while preserving surrounding structures.
These devices are classified as Class II under FDA regulations and are authorised via the 510(k) pathway. The company is based in the United States.
Catalogue
Carbodissecting Endoscope Ref K020925
Regimes: 510(k) Registry: 510(k)Carbodissecting Endoscope Ref K013680
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Endo Surgical Devices, Inc. have in the registry?
The registry currently lists 2 devices for Endo Surgical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Endo Surgical Devices, Inc.'s devices?
Among its 2 most recently registered devices, Endo Surgical Devices, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Endo Surgical Devices, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Endo Surgical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Endo Surgical Devices, Inc. in the registry?
The most recently registered devices listed for Endo Surgical Devices, Inc. include CARBODISSECTING ENDOSCOPE.