Duearity AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Duearity AB - FDA 510(k) Cleared Devices
Recent clearances: Tinearity G1 (6103)
1
Total
1
Cleared
0
Denied
Duearity AB has 1 FDA 510(k) cleared medical devices. Based in Malmo, SE.
Last cleared in 2023. Active since 2023. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Duearity AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Duearity AB
1 devices