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.

510(k) submissions have been managed by THEMA S.r.l. as regulatory consultant.

Tecnimed S.R.L. is one of 13017 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

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

5 devices

1-5 of 5

Data Source

Sourced from the FDA 510(k) public files . 175,972 total devices indexed.

Last updated: Sep 14, 2026