Globalmedia Group, LLC
Country not established
- Devices
- 1
What Globalmedia Group, LLC makes
Globalmedia Group, LLC manufactures the DERMA HOOD, a device designed for dermatological applications, likely intended for facial treatments or skincare procedures.
The DERMA HOOD is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Derma Hood Ref K131338
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Globalmedia Group, LLC have in the registry?
The registry currently lists 1 device for Globalmedia Group, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Globalmedia Group, LLC's devices?
Among its 1 most recently registered device, Globalmedia Group, LLC has devices listed in FDA 510(k) (1 device).
What risk classes do Globalmedia Group, LLC's devices fall under?
Among its 1 most recently registered device, the classes recorded for Globalmedia Group, LLC's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Globalmedia Group, LLC in the registry?
The most recently registered devices listed for Globalmedia Group, LLC include DERMA HOOD.