FDA Device Establishments · JSON-LD · Markdown
FEI 3007746785 · Manufacture Medical Device · Status: Active
| FEI Number | 3007746785 |
|---|---|
| Owner / Operator | LA.SC.OD. SPA (#8021059) |
| Address | VIA LONGO, 18 SESTO, FIORENTINO, FLORENCE, TUSCANY Firenze, 50019, IT |
| Mandatory US Agent | KROMOPAN U.S.A., INC. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | ELW |
| Regulation § (21 CFR) | 872.3660 |
| Proprietary names | Kromopan Sil Normal Set Kit - Putty Hard + Light Body; Oklurest; Kromopan Sil Putty Soft Fast Set; Ghenesyl Putty Soft Normal Set; Kromopan Sil Mono; Ghenesyl Putty Hard Normal Set; Ghenesyl Body Light Fast Set; Ghenesyl Body Regular Normal Set; Kromopan Sil Body Super Light Normal Set; Ghenesyl Putty Soft Fast Set |
Source: openFDA. Public-domain (CC0).