FDA Device Establishments · JSON-LD · Markdown
FEI 1000225541 · Manufacture Medical Device · Status: Active
| FEI Number | 1000225541 |
|---|---|
| Owner / Operator | Intensiv SA (#9001345) |
| Address | Via al Molino 107, Collina d'Oro / Montagnola Ticino, 6926, CH |
| Mandatory US Agent | REGISTRAR CORP |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EHM |
| Regulation § (21 CFR) | 872.6010 |
| Proprietary names | Intensiv Bevelshape; Intensiv ApproxOpener; Intensiv Ortho-Strips Opener; Intensiv Proxoshape; Intensiv Proxoshape Flexible; Intensiv Proxoshape Coarse; Intensiv ProxoStrip Anterior; Intensiv ProxoStrip; Intensiv Ortho-Strips Coarse; Intensiv ProxoPolish |
Source: openFDA. Public-domain (CC0).