FDA Device Establishments · JSON-LD · Markdown
FEI 1000116116 · Manufacture Medical Device for Another Party (Contract Manufacturer) · Status: Active
| FEI Number | 1000116116 |
|---|---|
| Owner / Operator | THE CRETEX COMPANIES, INC. (#9001389) |
| Address | 8600 EVERGREEN BLVD., MINNEAPOLIS, MN, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 4 |
| Product codes (top 20) | MNI, KWP, KWQ, MNH |
| Regulation § (21 CFR) | 888.3070, 888.3050, 888.3060 |
| Proprietary names | InCompass Thoracolumber Fusion System; InCompass System |
Source: openFDA. Public-domain (CC0).