FDA Device Establishments · JSON-LD · Markdown
FEI 3013505983 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3013505983 |
|---|---|
| Owner / Operator | Lumendi, LLC (#10054295) |
| Address | 253 Post Road W, Westport, CT, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | FDF |
| Regulation § (21 CFR) | 876.1500 |
| Proprietary names | DiLumen C2 |
Source: openFDA. Public-domain (CC0).