Teesuvac Aps is one of 44 FDA 510(k) medical device manufacturers from Denmark in the dataset, ranked by real submission volume.
Teesuvac Aps - FDA 510(k) Cleared Devices
Recent clearances: TeesuVac Breast Biopsy Device Mark 1
1
Total
1
Cleared
0
Denied
Teesuvac Aps has 1 FDA 510(k) cleared medical devices. Based in Hoersholm, DK.
Last cleared in 2022. Active since 2022. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Teesuvac Aps Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Teesuvac Aps
1 devices