# ESSILOR INTERNATIONAL, S.A.

FEI: 3004741385
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Essilor of America, Inc (#8010073)

Address: RUE FERNAND HOLWECK, DIJON Cote-d'Or, 21100, FR

Mandatory US Agent: EssilorLuxottica

## Products

Total registered: 1
Top product codes: HQG
Regulation §: 886.5844

Proprietary names: TruClear, Avance, DEFINITY 2, Xperio, Essilor Ideal, Varilux, Small Fit, Trivex, VARILUX-2, Presio i Approval

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223004741385%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3004741385