FDA Device Establishments · JSON-LD · Markdown
FEI 3005739886 · Manufacture Medical Device · Status: Active
| FEI Number | 3005739886 |
|---|---|
| Owner / Operator | Spinal USA, Inc. (#9087328) |
| Address | 2050 Executive Dr, Pearl, MS, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 5 |
| Product codes (top 20) | NKB, KWP, OSH, MNH, MNI |
| Regulation § (21 CFR) | 888.3070, 888.3050 |
| Proprietary names | REFORM HA COATED PEDICLE SCREW SYSTEM |
Source: openFDA. Public-domain (CC0).