FDA Device Establishments · JSON-LD · Markdown
FEI 3022777867 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3022777867 |
|---|---|
| Owner / Operator | Fixier S.A. de C.V. (#10085082) |
| Address | Carretera Doctor Mora a San Miguel de Allende km 3.4 Comunidad de San Rafael, Doctor Mora Guanajuato, 37967, MX |
| 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 | ALP titanium proximal tibia plate OPTIMUS 4 holes left, code 1534; ALP titanium distal tibia plate TIDIS 9 holes left, code 1119; 6.5mm cancellous screw 32mm thread 75mm, code 061.75; 4.5mm cortex screw 82mm, code 056.82; ALP titanium distal tibia plate TIDIS-II 7 holes right, code 1647; 4mm cancellous screw partially threaded 20mm, code 058.20; 2.7mm cortex screw 12mm, code 064.12; 6.5mm cancellous screw 16mm thread 85mm, code 060.85; ALP titanium proximal tibia plate OPTIMUS 12 holes left, code 153.12; 4.5mm titanium cortex screw 14mm, code 126.14 |
Source: openFDA. Public-domain (CC0).