# FGX EUROPE Ltd

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

## Products

Total registered: 1
Top product codes: HQZ
Regulation §: 886.5842

Proprietary names: Essilor, Luxottica

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221000304358%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1000304358