Romedex International Srl is one of 5624 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Romedex International Srl - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Romedex International Srl has 2 FDA 510(k) cleared medical devices. Based in Palo Alto, US.
Historical record: 2 cleared submissions from 2010 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Romedex International Srl Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Romedex International Srl
2 devices