FDA Device Establishments · JSON-LD · Markdown
FEI 3011015097 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3011015097 |
|---|---|
| Owner / Operator | Prosidyan, Inc. (#10047049) |
| Address | 41 Spring Street #107, New Providence, NJ, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MQV |
| Regulation § (21 CFR) | 888.3045 |
| Proprietary names | FIBERGRAFT BG PUTTY |
Source: openFDA. Public-domain (CC0).