FDA Device Establishments · JSON-LD · Markdown
FEI 3004474407 · Manufacture Device in the United States for Export Only · Status: Active
| FEI Number | 3004474407 |
|---|---|
| Owner / Operator | FZIOMED, INC. (#9034681) |
| Address | 231 BONETTI DR, San Luis Obispo, CA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | MCN |
| Proprietary names | Intercoat IU; Oxiplex/AP; Oxiplex/IU; Intercoat AP |
Source: openFDA. Public-domain (CC0).