FDA Device Establishments · JSON-LD · Markdown
FEI 3005893246 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3005893246 |
|---|---|
| Owner / Operator | NUTEK ORTHOPAEDICS, INC. (#9091870) |
| Address | 641 SW 3rd Ave, Fort Lauderdale, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KQZ |
| Regulation § (21 CFR) | 888.5890 |
| Proprietary names | First Assistant Reduction Device |
Source: openFDA. Public-domain (CC0).