Sordina S.p.A.
Country not established
- Devices
- 1
What Sordina S.p.A. makes
Sordina S.P.A. manufactures the LIAC, a device designed for laser-induced acoustic compression therapy, used primarily in dermatological and aesthetic treatments.
The LIAC is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Liac Ref K110840
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sordina S.P.A. have in the registry?
The registry currently lists 1 device for Sordina S.P.A.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sordina S.P.A.'s devices?
Among its 1 most recently registered device, Sordina S.P.A. has devices listed in FDA 510(k) (1 device).
What risk classes do Sordina S.P.A.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sordina S.P.A.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sordina S.P.A. in the registry?
The most recently registered devices listed for Sordina S.P.A. include LIAC.