Assut Europe S.P.A. is one of 19064 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Assut Europe S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: Assut Filbloc Permanent Sutures, ASSUFIL
2
Total
2
Cleared
0
Denied
Assut Europe S.P.A. has 2 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Historical record: 2 cleared submissions from 2002 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Assut Europe S.P.A. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Donawa Lifescience Consulting Srl as regulatory consultant.
FDA 510(k) Regulatory Record - Assut Europe S.P.A.
2 devices