Medical Device Manufacturer · US , Great Neck , NY

Tecnimed S.R.L. - FDA 510(k) Cleared Devices

5 submissions · 4 cleared · Since 2004

Total

Cleared

Denied

Tecnimed S.R.L. has 4 FDA 510(k) cleared medical devices. Based in Great Neck, US.

Historical record: 4 cleared submissions from 2004 to 2017. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Tecnimed S.R.L. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Tecnimed S.R.L.

5 devices

1-5 of 5