Biovica International AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Biovica International AB - FDA 510(k) Cleared Devices
Recent clearances: DiviTum TKa
1
Total
1
Cleared
0
Denied
Biovica International AB has 1 FDA 510(k) cleared medical devices. Based in Uppsala, SE.
Last cleared in 2022. Active since 2022. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Biovica International AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Biovica International AB
1 devices