Scandia Manufacturing, Ltd.
Country not established
- Devices
- 1
What Scandia Manufacturing, Ltd. makes
Scandia Manufacturing, Ltd. produces the Dermalife Hydrofusion Skin & Body Care System, a device designed for topical skin hydration and treatment.
The company’s portfolio is regulated under FDA 510(k) clearance as a Class II medical device and is listed in the U.S. regulatory database.
Catalogue
Dermalife Hydrofusion Skin & Body Care System Ref K003916
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Scandia Manufacturing, Ltd. have in the registry?
The registry currently lists 1 device for Scandia Manufacturing, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Scandia Manufacturing, Ltd.'s devices?
Among its 1 most recently registered device, Scandia Manufacturing, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Scandia Manufacturing, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Scandia Manufacturing, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Scandia Manufacturing, Ltd. in the registry?
The most recently registered devices listed for Scandia Manufacturing, Ltd. include DERMALIFE HYDROFUSION SKIN & BODY CARE SYSTEM.