Theken Companies, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theken Companies, LLC - FDA 510(k) Cleared Devices
Recent clearances: iNSitu Bipolar Hip System, iNSitu Total Hip System
4
Total
4
Cleared
0
Denied
Theken Companies, LLC has 4 FDA 510(k) cleared medical devices. Based in Akron, US.
Historical record: 4 cleared submissions from 2016 to 2019. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Theken Companies, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Biovera and BioVera, Inc..
FDA 510(k) Regulatory Record - Theken Companies, LLC
4 devices