Promethean Surgical Devices, Inc.
Country not established
- Devices
- 1
What Promethean Surgical Devices, Inc. makes
Promethean Surgical Devices, Inc. makes the Hydrocoat Mesh, a surgical mesh product used in medical procedures.
The Hydrocoat Mesh is classified as a Class II device and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
Hydrocoat Mesh Ref K090271
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Promethean Surgical Devices, Inc. have in the registry?
The registry currently lists 1 device for Promethean Surgical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Promethean Surgical Devices, Inc.'s devices?
Among its 1 most recently registered device, Promethean Surgical Devices, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Promethean Surgical Devices, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Promethean Surgical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Promethean Surgical Devices, Inc. in the registry?
The most recently registered devices listed for Promethean Surgical Devices, Inc. include HYDROCOAT MESH.