Bonebridge AG
Bonebridge AG holds FDA 510(k) medical device clearances, first cleared 2021, most recent 2026.
Top product codes for Bonebridge AG
Recent clearances by Bonebridge AG
- K261351 — SALGINA 2.5mm Distal Radius System
- K260228 — POYA 3.5mm Medial Proximal Tibia System
- K252191 — BRUSIO Trauma Toolbox System; TAMINA 3.5mm Proximal Humerus System
- K250933 — LORRAINE 2.5/3.5mm Distal Humerus System
- K243308 — Bonebridge Osteosynthesis Plating System (SALGINA 2.5mm Distal Radius System, CASCELLA 3.5mm Superior Clavicle System, LEPORELLO 3.5mm Olecranon Syste)
- K242399 — Bonebridge Osteosynthesis Plating System
- K240318 — SITTER 3.5mm Versatile System
- K231292 — TAMINA 3.5mm Proximal Humerus System; POYA 3.5MM Lateral Proximal Tibia System; LORRAINE 3.5mm Distal Humerus System
- K213864 — Bonebridge Osteosynthesis Plating System
- K203002 — SALGINA 2.5mm Volar Distal Radius System, CASCELLA 3.5mm Superior Clavicle System, TAMlNA 3.5mm Proximal Humerus System, TRIFT 3.5mm 1/3 Tubular System
Data sourced from openFDA. This site is unofficial and independent of the FDA.