FDA Device Establishments · JSON-LD · Markdown
FEI 3021010222 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3021010222 |
|---|---|
| Owner / Operator | Bonebridge AG (#10083420) |
| Address | Bahnhofstrasse 11, ZUG, 6300, CH |
| Mandatory US Agent | confinis USA Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | HWC, HRS |
| Regulation § (21 CFR) | 888.3040, 888.3030 |
| Proprietary names | TAMINA 3.5mm Proximal Humerus System; POYA 3.5mm Lateral Proximal Tibia System; LORRAINE 3.5mm Distal Humerus System |
Source: openFDA. Public-domain (CC0).