Biolight AB
SwedenFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Biolight Biodynam Ref K130866
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biolight AB have in the registry?
The registry currently lists 1 device for Biolight AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biolight AB's devices?
Among its 1 most recently registered device, Biolight AB has devices listed in FDA 510(k) (1 device).
What risk classes do Biolight AB's devices fall under?
Among its 1 most recently registered device, the classes recorded for Biolight AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biolight AB in the registry?
The most recently registered devices listed for Biolight AB include BIOLIGHT BIODYNAM.