Biovica International AB
SwedenFDA applicant, unverified FDA FEI 3008629194
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Registry: GUDID
DiviTum TKa Ref K202852
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3008629194
- DUNS number
- 776734126
- Address
- Uppsala Science Park, Uppsala
- [email protected]
- Phone
- +1 (858) 230-6044
Frequently asked questions
How many devices does Biovica International AB have in the registry?
The registry currently lists 2 devices for Biovica International AB. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biovica International AB's devices?
Among its 2 most recently registered devices, Biovica International AB has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Biovica International AB's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Biovica International AB's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biovica International AB in the registry?
The most recently registered devices listed for Biovica International AB include DiviTum®TKa 95010 and DiviTum TKa.