FDA Device Establishments · JSON-LD · Markdown
FEI 3023805 · Manufacture Medical Device · Status: Active
| FEI Number | 3023805 |
|---|---|
| Owner / Operator | Leander, LLC (#3023805) |
| Address | 1400 E 24th St Ste C, Lawrence, KS, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | LGX |
| Regulation § (21 CFR) | 878.4960 |
| Proprietary names | Flexion Distraction Table |
Source: openFDA. Public-domain (CC0).