Ams is one of 221 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Ams - FDA 510(k) Cleared Devices
Recent clearances: Eclipse Kiss Zirconia, LIASYS 450
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: Chemistry.
Browse the FDA 510(k) cleared devices submitted by Ams Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Onbix Corporation as regulatory consultant.
FDA 510(k) Regulatory Record - Ams
2 devices