Medical Device Manufacturer · ES , Barcelona

Leventon, S.A. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1985

Total

Cleared

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.

FDA 510(k) Regulatory Record - Leventon, S.A.

5 devices

1-5 of 5