Avanti Orthopaedics, LLC

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K261145Avanti Distal Elbow ORIF SystemMay 9, 2026
K222967Avanti Orthopaedics 2.2mm and 2.7mm Cannulated Screws, Avanti Orthopaedics 3.2mm and 4.0mm CannulateNovember 23, 2022
K211592Avanti Orthopaedics Ulnar Shortening SystemJuly 16, 2021
K191118Avanti Distal Radius and Forearm SystemDecember 13, 2019