Syncare Corp.
Country not established
- Devices
- 1
What Syncare Corp. makes
Syncare Corp. manufactures NOVADERM, a Class I medical device designed for skin treatment applications, likely including wound care or dermatological procedures.
NOVADERM 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
Novaderm Ref K896531
510(k) 510(k)
Frequently asked questions
How many devices does Syncare Corp. have in the registry?
The registry currently lists 1 device for Syncare Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Syncare Corp.'s devices?
Among its 1 most recently registered device, Syncare Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Syncare Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Syncare Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Syncare Corp. in the registry?
The most recently registered devices listed for Syncare Corp. include NOVADERM.