FDA Device Establishments · JSON-LD · Markdown

FGX EUROPE Ltd

FEI 1000304358 · Repack or Relabel Medical Device Export Device to the United States But Perform No Other Operation on Device · Status: Active

FEI Number1000304358
Owner / OperatorEssilor of America, Inc (#8010073)
Address50 Broadway, Suite 1, 7th Floor, London London, City of, SW1H OBL, GB
Mandatory US AgentEssilorLuxottica
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HQZ
Regulation § (21 CFR)886.5842
Proprietary namesEssilor; Luxottica

External sources

Source: openFDA. Public-domain (CC0).