Dermgard, Inc.
Country not established
- Devices
- 1
What Dermgard, Inc. makes
Dermgard, Inc. manufactures the Dermgard System 800 and 900, which are medical devices designed for dermatological procedures, likely involving controlled energy delivery for skin treatments or minor surgical applications.
These devices fall under FDA Class II regulation and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Dermgard System 800 And 900 Ref K880486
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermgard, Inc. have in the registry?
The registry currently lists 1 device for Dermgard, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermgard, Inc.'s devices?
Among its 1 most recently registered device, Dermgard, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dermgard, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dermgard, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermgard, Inc. in the registry?
The most recently registered devices listed for Dermgard, Inc. include DERMGARD SYSTEM 800 AND 900.