# EYEQUE CORPORATION

FEI: 3013003882
Status: Active
Establishment types: Develop Specifications But Do Not Manufacture At This Facility; Repack or Relabel Medical Device
Owner/operator: EYEQUE (#10052589)

Address: 39608 Eureka Dr, Newark, CA, US



## Products

Total registered: 1
Top product codes: HKO
Regulation §: 886.1760

Proprietary names: EyeQue VisionCheck, VisionCheck

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223013003882%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3013003882