Tenon Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tenon Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CATAMARAN SI Joint Fusion System, Catamaran Sacroiliac Joint Fixation System (CAT SIJ Fixation System)
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.
Regulatory submissions have been managed by Jgc, LLC and Lince Consulting, LLC.
FDA 510(k) Regulatory Record - Tenon Medical, Inc.
2 devices