Germitec is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Germitec - FDA 510(k) Cleared Devices
1
Total
0
Cleared
1
Denied
Germitec has 0 FDA 510(k) cleared medical devices. Based in Bordeaux, FR.
Active since 2024. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Germitec Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Germitec
1 devices