FDA Device Establishments · JSON-LD · Markdown
FEI 3004499989 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3004499989 |
|---|---|
| Owner / Operator | LIFE SPINE (#9061495) |
| Address | 13951 Quality Dr, Huntley, IL, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | NKB |
| Regulation § (21 CFR) | 888.3070 |
| Proprietary names | ARx |
Source: openFDA. Public-domain (CC0).