Gmg Enterprises, Inc.
Country not established
- Devices
- 1
What Gmg Enterprises, Inc. makes
Gmg Enterprises, Inc. manufactures the Pulsor, a therapeutic vibrator designed for medical use.
The company’s portfolio is regulated under FDA’s Class I device classification and is listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Pulsor, Therapeutic Vibrator Ref K874716
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gmg Enterprises, Inc. have in the registry?
The registry currently lists 1 device for Gmg Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gmg Enterprises, Inc.'s devices?
Among its 1 most recently registered device, Gmg Enterprises, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Gmg Enterprises, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gmg Enterprises, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gmg Enterprises, Inc. in the registry?
The most recently registered devices listed for Gmg Enterprises, Inc. include PULSOR, THERAPEUTIC VIBRATOR.