Tigon Medical

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252596Tigon Medical Knotless and Dual Javelin All-Suture AnchorsDecember 4, 2025
K242529Tigon Medical All-Suture Anchors (ASA)December 20, 2024
K240175Tigon Medical Fractures, Instability, and Reconstruction (FIRE)October 29, 2024
K220464Tigon Medical Gryphon Anchor LineMarch 22, 2023
K211049Tigon Medical Button SystemAugust 4, 2021
K182507Tigon Medical Tissue AnchorsJanuary 21, 2019