Depuy International, Ltd. is one of 195 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Depuy International, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DePuy 3D Additive TriFlange Acetabular Cup
1
Total
1
Cleared
0
Denied
Depuy International, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Leeds, GB.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Depuy International, Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by DePuy Orthopaedics, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Depuy International, Ltd.
1 devices