Suzhou Endophix Co., Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K232941Megaloop Button SystemMay 3, 2024
K232725Javelot Ti Suture Anchor, Javelot Ti-D Suture AnchorNovember 2, 2023
K231002Javelot PK-S suture anchor, Javelot PK-S suture anchor (Knotless), Javelot PK-P suture anchor, JavelJune 7, 2023
K230874Syntheface PEEK Interference Screw, Syntheface PEEK Screw SheathMay 23, 2023