Sanuthera, Inc.
Country not established
- Devices
- 1
What Sanuthera, Inc. makes
Sanuthera, Inc. makes the Serenity device.
The Serenity device is a Class II medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Serenity Ref K150014
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sanuthera, Inc. have in the registry?
The registry currently lists 1 device for Sanuthera, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sanuthera, Inc.'s devices?
Among its 1 most recently registered device, Sanuthera, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Sanuthera, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sanuthera, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Sanuthera, Inc. in the registry?
The most recently registered devices listed for Sanuthera, Inc. include Serenity.