Dermaco, Inc.
Country not established
- Devices
- 1
What Dermaco, Inc. makes
Dermaco, Inc. manufactures the DERMCO A-I, a Class I medical device designed for dermatological applications, likely intended for skin treatment or diagnostic procedures.
The DERMCO A-I is regulated under the FDA’s 510(k) pathway as a Class I device and is listed in the U.S. regulatory database. The company is based in the United States.
Catalogue
Dermco A-I Ref K923400
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermaco, Inc. have in the registry?
The registry currently lists 1 device for Dermaco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermaco, Inc.'s devices?
Among its 1 most recently registered device, Dermaco, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dermaco, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dermaco, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Dermaco, Inc. in the registry?
The most recently registered devices listed for Dermaco, Inc. include DERMCO A-I.