FDA Device Establishments · JSON-LD · Markdown
FEI 3012479318 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 3012479318 |
|---|---|
| Owner / Operator | Biovico Sp. z o.o. (#10060839) |
| Address | 7, Skandynawska Street, Wladyslawowo Pomorskie, PL-84-120, PL |
| Mandatory US Agent | Registrar Corp |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GXQ |
| Regulation § (21 CFR) | 882.5910 |
| Proprietary names | SyntheCel Dura Repair |
Source: openFDA. Public-domain (CC0).