Tenon Medical, Inc. - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Tenon Medical, Inc. has 2 FDA 510(k) cleared medical devices. Based in San Ramon, US.
Last cleared in 2023. Active since 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Tenon Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Lince Consulting, LLC as regulatory consultant.
2 devices