Medical Device Manufacturer · IT , Poggio Rusco

Medax Srl Unipersonale - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2015

Total

Cleared

Denied

Medax Srl Unipersonale has 5 FDA 510(k) cleared medical devices. Based in Poggio Rusco, IT.

Historical record: 5 cleared submissions from 2015 to 2020. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Medax Srl Unipersonale Filter by specialty or product code using the sidebar.

Regulatory submissions have been managed by Gemarmed S.R.L and Coronati Consulting Srl.

Medax Srl Unipersonale 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 - Medax Srl Unipersonale

5 devices

1-5 of 5

Data Source

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

Last updated: May 28, 2026