EYEQUE CORPORATION

FDA Device Registration & Listing · Newark, CA, US · Registration 3013003882

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3013003882
FEI Number
3013003882
Entity Name
EYEQUE CORPORATION
City/State/Country
Newark, CA, US
Establishment Address
39608 Eureka Dr, Newark, CA 94560, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device
Owner / Operator
EYEQUE (Owner Number: 10052589)
Owner / Operator Contact Address
39608 Eureka Drive, Newark, CA 94560, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

PVT Lite EyeQue VERAI VERAI EyeQye PVT Lite EyeQue Try-On Glasses VERAI Try-On Glasses EyeQue VERAI Insight Pro EyeQue Insight Lite Insight EyeQue Insight EyeQue VERAI Insight Lite EyeQue Insight Pro VERAI EyeQue VERAI EyeQue Connect VERAI EyeQue VisionCheck VisionCheck EyeQue Insight Insight Insight Lite EyeQue Insight Lite EyeQue Insight Pro Insight Pro

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HKN Refractor, Manual, Non-Powered, Including Phoropter Ophthalmic Class 1 886.1770 2024-05-31
HPA Frame, Trial, Ophthalmic Ophthalmic Class 1 886.1415 2021-08-12
HOX Chart, Visual Acuity Ophthalmic Class 1 886.1150 2018-01-24
OUG Medical Device Data System General Hospital Class 1 880.6310 2022-10-26
HKO Refractometer, Ophthalmic Ophthalmic Class 1 886.1760 2016-08-22
HIT Tester, Color Vision Ophthalmic Class 1 886.1170 2021-07-09

Official Correspondent

Noam Sapiens

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EYEQUE
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013003882. Last updated year: 2026. Please use registration number 3013003882 when referencing this establishment in official correspondence.
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