Ascom Ums Srl Unipersonale is one of 227 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Ascom Ums Srl Unipersonale - FDA 510(k) Cleared Devices
Recent clearances: Digistat Care, Digistat Smart Central
2
Total
2
Cleared
0
Denied
Ascom Ums Srl Unipersonale has 2 FDA 510(k) cleared medical devices. Based in Scandicci (Fi), IT.
Latest FDA clearance: Sep 2026. Active since 2018. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Ascom Ums Srl Unipersonale Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Speed TO Market, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Ascom Ums Srl Unipersonale
2 devices