FDA Device Establishments · JSON-LD · Markdown
FEI 3043234953 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3043234953 |
|---|---|
| Owner / Operator | ALLUMIN8 INC (#10095187) |
| Address | 3158 W Lakefront Ct, Springfield, MO, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | NKB |
| Regulation § (21 CFR) | 888.3070 |
| Proprietary names | ALLUMIN8® A8 INTEGR8 Porous Pedicle Screw System |
Source: openFDA. Public-domain (CC0).