FDA Device Establishments · JSON-LD · Markdown
FEI 3009401421 · Repack or Relabel Medical Device Develop Specifications But Do Not Manufacture At This Facility Complaint File Establishment per 21 CFR 820.198 · Status: Active
| FEI Number | 3009401421 |
|---|---|
| Owner / Operator | Opia Technologies SAS (#10042009) |
| Address | 17 Rue Moreau, Paris, 75012, FR |
| Mandatory US Agent | The Nilson Law Group PLLC |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KET |
| Regulation § (21 CFR) | 864.3010 |
| Proprietary names | EYEPRIM |
Source: openFDA. Public-domain (CC0).