FDA Device Establishments · JSON-LD · Markdown
FEI 3020491484 · Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3020491484 |
|---|---|
| Owner / Operator | Luminance Medical Ventures Incorporated (#10082015) |
| Address | 5752 Grandscape Blvd Ste 225, The Colony, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OKJ |
| Regulation § (21 CFR) | 878.4860 |
| Proprietary names | Lumiance RED Cold Sore Device |
Source: openFDA. Public-domain (CC0).