Cinventa AB
SwedenFDA applicant, unverified
- Devices
- 1
What Cinventa AB makes
Cinventa AB manufactures the BABYROCKER, a Class II medical device designed for infant care.
The BABYROCKER is regulated as a Class II device and is listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Babyrocker Ref K881019
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cinventa AB have in the registry?
The registry currently lists 1 device for Cinventa AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cinventa AB's devices?
Among its 1 most recently registered device, Cinventa AB has devices listed in FDA 510(k) (1 device).
What risk classes do Cinventa AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cinventa AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cinventa AB in the registry?
The most recently registered devices listed for Cinventa AB include BABYROCKER.