Comeg USA, Inc.
Country not established
- Devices
- 1
What Comeg USA, Inc. makes
Comeg USA, Inc. manufactures arthroscopes, which are endoscopes used for visualizing, diagnosing, and treating joint conditions within the knee, shoulder, and other articulations.
The company’s arthroscopes are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearance records. The manufacturer is based in the United States.
Catalogue
Arthroscope Ref K862275
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Comeg USA, Inc. have in the registry?
The registry currently lists 1 device for Comeg USA, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Comeg USA, Inc.'s devices?
Among its 1 most recently registered device, Comeg USA, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Comeg USA, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Comeg USA, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Comeg USA, Inc. in the registry?
The most recently registered devices listed for Comeg USA, Inc. include ARTHROSCOPE.