FDA Device Establishments · JSON-LD · Markdown
FEI 3008087383 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3008087383 |
|---|---|
| Owner / Operator | GEODIS (#10030802) |
| Address | 450 Lillard Drive, Sparks, NV, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | LRC, PGW |
| Regulation § (21 CFR) | 874.4420, 882.4560 |
| Proprietary names | SPINPLUS 3-GUIDE |
Source: openFDA. Public-domain (CC0).