FDA Device Establishments · JSON-LD · Markdown
FEI 3004837462 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3004837462 |
|---|---|
| Owner / Operator | Synthon Hispania S.L. (#10092498) |
| Address | CALLE Castello, 1 - PG SALINAS, Sant Boi de Llobregat Barcelona, 08830, ES |
| Mandatory US Agent | Lachman Consultant Services, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KZH |
| Regulation § (21 CFR) | 880.6920 |
| Proprietary names | GripMate |
Source: openFDA. Public-domain (CC0).