Bonebridge AG

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K252191BRUSIO Trauma Toolbox System; TAMINA 3.5mm Proximal Humerus SystemDecember 17, 2025
K250933LORRAINE 2.5/3.5mm Distal Humerus SystemJune 11, 2025
K243308Bonebridge Osteosynthesis Plating System (SALGINA 2.5mm Distal Radius System, CASCELLA 3.5mm SuperioDecember 20, 2024
K242399Bonebridge Osteosynthesis Plating SystemOctober 31, 2024
K240318SITTER 3.5mm Versatile SystemAugust 23, 2024
K231292TAMINA 3.5mm Proximal Humerus System; POYA 3.5MM Lateral Proximal Tibia System; LORRAINE 3.5mm DistaJuly 19, 2023
K213864Bonebridge Osteosynthesis Plating SystemSeptember 2, 2022
K203002SALGINA 2.5mm Volar Distal Radius System, CASCELLA 3.5mm Superior Clavicle System, TAMlNA 3.5mm ProxOctober 5, 2021