FDA Device Establishments · JSON-LD · Markdown
FEI 1000304358 · Repack or Relabel Medical Device Export Device to the United States But Perform No Other Operation on Device · Status: Active
| FEI Number | 1000304358 |
|---|---|
| Owner / Operator | Essilor of America, Inc (#8010073) |
| Address | 50 Broadway, Suite 1, 7th Floor, London London, City of, SW1H OBL, GB |
| Mandatory US Agent | EssilorLuxottica |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | HQZ |
| Regulation § (21 CFR) | 886.5842 |
| Proprietary names | Essilor; Luxottica |
Source: openFDA. Public-domain (CC0).