FDA Device Establishments · JSON-LD · Markdown
FEI 3016237718 · Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3016237718 |
|---|---|
| Owner / Operator | LuxCreo Inc. (#10071055) |
| Address | 350 W. Ontario Street Suite 700 Chicago,lL.60654, Chicago, IL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 2 |
| Product codes (top 20) | KMY, MQC |
| Regulation § (21 CFR) | 872.5525 |
| Proprietary names | LuxCreo Dental Night Guard Resin |
Source: openFDA. Public-domain (CC0).