FDA Device Establishments · JSON-LD · Markdown
FEI 3030626336 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device · Status: Active
| FEI Number | 3030626336 |
|---|---|
| Owner / Operator | Magentiq Eye Ltd (#10090333) |
| Address | 6 Ben-Gurion Blvd., Haifa, 3541416, IL |
| Mandatory US Agent | Medical Device Post-Production Services, Inc. |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | QNP |
| Regulation § (21 CFR) | 876.1520 |
| Proprietary names | MAGENTIQ-COLO; ME-APDS |
Source: openFDA. Public-domain (CC0).