The Gotzen Group, Inc.
Country not established
- Devices
- 1
What The Gotzen Group, Inc. makes
The Gotzen Group, Inc. manufactures the DEGOTZEN SYNCHRO device.
This device is classified as Class II and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Degotzen Synchro Ref K021245
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does The Gotzen Group, Inc. have in the registry?
The registry currently lists 1 device for The Gotzen Group, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Gotzen Group, Inc.'s devices?
Among its 1 most recently registered device, The Gotzen Group, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do The Gotzen Group, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for The Gotzen Group, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Gotzen Group, Inc. in the registry?
The most recently registered devices listed for The Gotzen Group, Inc. include DEGOTZEN SYNCHRO.