FDA Device Establishments · JSON-LD · Markdown

EYEQUE CORPORATION

FEI 3013003882 · Develop Specifications But Do Not Manufacture At This Facility Repack or Relabel Medical Device · Status: Active

FEI Number3013003882
Owner / OperatorEYEQUE (#10052589)
Address39608 Eureka Dr, Newark, CA, US
Registration expiry2026
Initial importer flagN
Registered products1
Product codes (top 20)HKO
Regulation § (21 CFR)886.1760
Proprietary namesEyeQue VisionCheck; VisionCheck

External sources

Source: openFDA. Public-domain (CC0).