Castellini S.P.A. is one of 227 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.
Castellini S.P.A. - FDA 510(k) Cleared Devices
Recent clearances: LOGOS JUNIOR DENTAL CHAIR AND UNIT, CASTELLNI AIR POWERED HANDPIECES SYRINGES: THREE STERIL, MULTISTERIL TURBINS: CLEANAIR, CLEANLIGHT MICROMOTORS: IMPLANTO, PUMA DENTAL CHAIR AND UNIT
4
Total
4
Cleared
0
Denied
Castellini S.P.A. has 4 FDA 510(k) cleared medical devices. Based in Italy, IT.
Historical record: 4 cleared submissions from 1994 to 2003. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Castellini S.P.A. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Castellini S.P.A.
4 devices