FDA Device Establishments · JSON-LD · Markdown
FEI 3004717358 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3004717358 |
|---|---|
| Owner / Operator | SPINECRAFT LLC (#9065601) |
| Address | 777 Oakmont Ln Suite 200, Westmont, IL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | MAX, ODP |
| Regulation § (21 CFR) | 888.3080 |
| Proprietary names | ORIO-Ti Intervertebral Body Fusion Cage System |
Source: openFDA. Public-domain (CC0).