Dermacare, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Dermacare, Inc. makes
Dermacare, Inc. manufactures THERMACLEAR, a medical device designed for controlled thermal treatment of skin conditions.
The device is classified as Class II under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.
Catalogue
Dermacare Tie Holder Ref K893995
Regimes: 510(k) Registry: 510(k)Disposable Bipolar Cord And Bipolar Forcep Ref K884656
Regimes: 510(k) Registry: 510(k)Thermaclear Ref K060653
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermacare, Inc. have in the registry?
The registry currently lists 3 devices for Dermacare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermacare, Inc.'s devices?
Among its 3 most recently registered devices, Dermacare, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Dermacare, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Dermacare, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermacare, Inc. in the registry?
The most recently registered devices listed for Dermacare, Inc. include DERMACARE TIE HOLDER, DISPOSABLE BIPOLAR CORD AND BIPOLAR FORCEP and THERMACLEAR.