Leventon, S.A. is one of 85 FDA 510(k) medical device manufacturers from Spain in the dataset, ranked by real submission volume.
Leventon, S.A. - FDA 510(k) Cleared Devices
Recent clearances: SPIRO-BALL, DOSI-FUSER, TRI-BALL
5
Total
5
Cleared
0
Denied
Leventon, S.A. has 5 FDA 510(k) cleared medical devices. Based in Barcelona, ES.
Historical record: 5 cleared submissions from 1985 to 2005. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Leventon, S.A. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Leventon, S.A.
5 devices