Depuy France S.A.S. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Depuy France S.A.S. - FDA 510(k) Cleared Devices
Recent clearances: DePuy Corail AMT Hip Prosthesis
2
Total
2
Cleared
0
Denied
Depuy France S.A.S. has 2 FDA 510(k) cleared medical devices. Based in Warsaw, US.
Historical record: 2 cleared submissions from 2013 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Depuy France S.A.S. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Depuy France S.A.S.
2 devices