Ams is one of 110 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Ams - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Ams has 2 FDA 510(k) cleared medical devices. Based in Guidonia, Rome, IT.
Historical record: 2 cleared submissions from 2012 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ams Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ams
2 devices