Bonebridge AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Bonebridge AG - FDA 510(k) Cleared Devices
Recent clearances: POYA 3.5mm Medial Proximal Tibia System, BRUSIO Trauma Toolbox System, LORRAINE 2.5/3.5mm Distal Humerus System
10
Total
10
Cleared
0
Denied
Bonebridge AG has 10 FDA 510(k) cleared orthopedic devices. Based in Zug, CH.
Latest FDA clearance: Jun 2026. Active since 2021.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Meditec Consulting GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Bonebridge AG
10 devices
Cleared
Jun 26, 2026
SALGINA 2.5mm Distal Radius System
Orthopedic
63d
Cleared
Apr 24, 2026
POYA 3.5mm Medial Proximal Tibia System
Orthopedic
88d
Cleared
Dec 17, 2025
BRUSIO Trauma Toolbox System
Orthopedic
156d
Cleared
Jun 11, 2025
LORRAINE 2.5/3.5mm Distal Humerus System
Orthopedic
75d
Cleared
Dec 20, 2024
Bonebridge Osteosynthesis Plating System (SALGINA 2.5mm Distal Radius System,...
Orthopedic
60d
Cleared
Oct 31, 2024
Bonebridge Osteosynthesis Plating System
Orthopedic
79d
Cleared
Aug 23, 2024
SITTER 3.5mm Versatile System
Orthopedic
203d
Cleared
Jul 19, 2023
TAMINA 3.5mm Proximal Humerus System
Orthopedic
76d
Cleared
Sep 02, 2022
Bonebridge Osteosynthesis Plating System
Orthopedic
266d
Cleared
Oct 05, 2021
SALGINA 2.5mm Volar Distal Radius System, CASCELLA 3.5mm Superior Clavicle...
Orthopedic
369d