Bonebridge AG
Bonebridge AG appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Jun 26, 2026.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K261351 | SALGINA 2.5mm Distal Radius System | Jun 26, 2026 |
| K260228 | POYA 3.5mm Medial Proximal Tibia System | Apr 24, 2026 |
| K252191 | BRUSIO Trauma Toolbox System; TAMINA 3.5mm Proximal Humerus System | Dec 17, 2025 |
| K250933 | LORRAINE 2.5/3.5mm Distal Humerus System | Jun 11, 2025 |
| K243308 | Bonebridge Osteosynthesis Plating System (SALGINA 2.5mm Distal Radius System, CASCELLA 3.5mm Superio | Dec 20, 2024 |
| K242399 | Bonebridge Osteosynthesis Plating System | Oct 31, 2024 |
| K240318 | SITTER 3.5mm Versatile System | Aug 23, 2024 |
| K231292 | TAMINA 3.5mm Proximal Humerus System; POYA 3.5MM Lateral Proximal Tibia System; LORRAINE 3.5mm Dista | Jul 19, 2023 |
| K213864 | Bonebridge Osteosynthesis Plating System | Sep 2, 2022 |
| K203002 | SALGINA 2.5mm Volar Distal Radius System, CASCELLA 3.5mm Superior Clavicle System, TAMlNA 3.5mm Prox | Oct 5, 2021 |