The Gid Group, Inc.
Country not established
- Devices
- 1
What The Gid Group, Inc. makes
The Gid Group, Inc. manufactures the GID 700, which is a Class II medical device.
The company is based in the US and its devices are listed in the FDA 510(k) registry.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Gid 700 Ref K120902
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Gid Group, Inc. have in the registry?
The registry currently lists 1 device for The Gid Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Gid Group, Inc.'s devices?
Among its 1 most recently registered device, The Gid Group, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do The Gid Group, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Gid Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Gid Group, Inc. in the registry?
The most recently registered devices listed for The Gid Group, Inc. include GID 700.