Fin-Ceramica Faenza S.P.A. is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Fin-Ceramica Faenza S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: CustomizedBone Service, CustomizedBone Service, CustomizedBone Service
5
Total
5
Cleared
0
Denied
Fin-Ceramica Faenza S.P.A. has 5 FDA 510(k) cleared medical devices. Based in Faenza, IT.
Latest FDA clearance: Mar 2024. Active since 2016. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Fin-Ceramica Faenza S.P.A. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Regulatory and Clinical Research Institute, Inc. and Fortrea.
FDA 510(k) Regulatory Record - Fin-Ceramica Faenza S.P.A.
5 devices