Tenon Medical, Inc.

FDA Regulatory Profile

Tenon Medical, Inc. appears in FDA public data with 0 recalls, 4 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 8, 2026.

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260477CATAMARAN™ SI Joint Fusion SystemApril 8, 2026
K250403Catamaran SI Joint Fusion SystemMarch 21, 2025
K231944CATAMARAN SI Joint Fusion SystemAugust 24, 2023
K180818Catamaran Sacroiliac Joint Fixation System (CAT SIJ Fixation System)June 13, 2018