Bespoke Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Bespoke Technologies - FDA 510(k) Cleared Devices
Recent clearances: Tailored-C Cervical Interbody Fusion System
1
Total
1
Cleared
0
Denied
Bespoke Technologies has 1 FDA 510(k) cleared medical devices. Based in Winston-Salemn, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Bespoke Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Bespoke Technologies
1 devices