FDA Device Establishments · JSON-LD · Markdown
FEI 3011501130 · Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3011501130 |
|---|---|
| Owner / Operator | Actegy Ltd. (#10044804) |
| Address | 7320 NW 12th Street,, Suite 103 Doral,, Miami, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 2 |
| Product codes (top 20) | NGX, NUH |
| Regulation § (21 CFR) | 890.5850, 882.5890 |
| Proprietary names | Revitive Circulation Booster |
Source: openFDA. Public-domain (CC0).