Theken Companies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theken Companies - FDA 510(k) Cleared Devices
Recent clearances: Mg-PSZ Ceramic Femoral Head
1
Total
1
Cleared
0
Denied
Theken Companies has 1 FDA 510(k) cleared medical devices. Based in Akron, US.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Theken Companies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by BioVera, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Theken Companies
1 devices