# Essilor Asia Pacific PTE LTD

FEI: 3007529446
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: Essilor of America, Inc (#8010073)

Address: 215 Kallang Bahru, No. 04-00, Singapore Central Singapore, 33934657, SG

Mandatory US Agent: EssilorLuxottica

## Products

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

Proprietary names: Presio i Approval

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223007529446%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3007529446