Met One Technologies

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K251732Wrist Fracture SystemFebruary 12, 2026
K250866Sovereign Posterior Cervical SystemMay 20, 2025
K230851Kodiak Lumbar Spacer SystemMay 26, 2023
K222806Kodiak C Spinal Implant SystemDecember 22, 2022
K193457AUDERE Lumbar Spacer SystemMay 12, 2020
K180772Met One Czar Anterior Cervical Plate SystemDecember 17, 2018
K170108Xultan 5.5 Pedicle Screw SystemMay 2, 2017