Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in SwitzerlandLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under its name, each linked to the record.
As of Nov 13, 2026, FDA's public records list Bonebridge AG with 10 510(k) clearances. The most recent is a 510(k) clearance dated Jun 26, 2026: SALGINA 2.5mm Distal Radius System.
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Date | Record | Source |
|---|---|---|
| Jun 26, 2026 | SALGINA 2.5mm Distal Radius SystemK261351 · HRS | 510(k) clearances |
| Apr 24, 2026 | POYA 3.5mm Medial Proximal Tibia SystemK260228 · HRS | 510(k) clearances |
| Dec 17, 2025 | BRUSIO Trauma Toolbox System; TAMINA 3.5mm Proximal Humerus SystemK252191 · HRS | 510(k) clearances |
| Jun 11, 2025 | LORRAINE 2.5/3.5mm Distal Humerus SystemK250933 · HRS | 510(k) clearances |
| Dec 20, 2024 | Bonebridge Osteosynthesis Plating System (SALGINA 2.5mm Distal Radius System, CASCELLA 3.5mm Superior Clavicle System, LEPORELLO 3.5mm Olecranon Syste)K243308 · HRS | 510(k) clearances |
| Oct 31, 2024 | Bonebridge Osteosynthesis Plating SystemK242399 · HRS | 510(k) clearances |
| Aug 23, 2024 | SITTER 3.5mm Versatile SystemK240318 · HRS | 510(k) clearances |
| Jul 19, 2023 | TAMINA 3.5mm Proximal Humerus System; POYA 3.5MM Lateral Proximal Tibia System; LORRAINE 3.5mm Distal Humerus SystemK231292 · HRS | 510(k) clearances |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
