EYENUK

FDA Device Registration & Listing · Woodland Hills, CA, US · Registration 3013924858

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
3013924858
FEI Number
3013924858
Entity Name
EYENUK
City/State/Country
Woodland Hills, CA, US
Establishment Address
5850 Canoga Ave, Suite 250, Woodland Hills, CA 91367, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Eyenuk (Owner Number: 10077823)
Owner / Operator Contact Address
5850 Canoga Ave, Suite 250, Woodland Hills, CA 91367, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K200667
PMA Number
N/A

All Registered Proprietary Names

EyeArt

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
PIB Diabetic Retinopathy Detection Device Ophthalmic Class 2 886.1100 2020-10-02

Official Correspondent

Malavika Bhaskaranand

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Eyenuk
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 3013924858. Last updated year: 2026. Please use registration number 3013924858 when referencing this establishment in official correspondence.
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