Medical Device Manufacturer · IT , Rome

Teva Medical Ltd., Migada Plant - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2014

Total

Cleared

Denied

Teva Medical Ltd., Migada Plant has 4 FDA 510(k) cleared medical devices. Based in Rome, IT.

Historical record: 4 cleared submissions from 2014 to 2018. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Teva Medical Ltd., Migada Plant Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Donawa Lifescience Consulting as regulatory consultant.

Teva Medical Ltd., Migada Plant is one of 126 FDA 510(k) medical device manufacturers from Italy in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Teva Medical Ltd., Migada Plant

4 devices

1-4 of 4

Data Source

Sourced from the FDA 510(k) public files . 175,218 total devices indexed.

Last updated: Jun 08, 2026