Entomed AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Entomed AB - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Entomed AB has 1 FDA 510(k) cleared medical devices. Based in Malmo, SE.
Historical record: 1 cleared submissions from 2009 to 2009. Primary specialty: Ear, Nose, Throat.
Browse the FDA 510(k) cleared devices submitted by Entomed AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Entomed AB
1 devices