Medex is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Medex - FDA 510(k) Cleared Devices
Recent clearances: Qitexio® 4-Way Stopcock (QIT014), Qitexio
2
Total
2
Cleared
0
Denied
Medex has 2 FDA 510(k) cleared medical devices. Based in Saint-Priest, FR.
Latest FDA clearance: Apr 2025. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medex Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Guerbet, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medex
2 devices