Odon Lifetechnology is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Odon Lifetechnology - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Odon Lifetechnology has 1 FDA 510(k) cleared medical devices. Based in Neuilly Sur Seine, FR.
Historical record: 1 cleared submissions from 2000 to 2000. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Odon Lifetechnology Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Odon Lifetechnology
1 devices