WALMART INC.

FDA Device Registration & Listing · BENTONVILLE, AR, US · Registration 2316750

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
2316750
FEI Number
2316750
Entity Name
WALMART INC.
City/State/Country
BENTONVILLE, AR, US
Establishment Address
811 Excellence Drive, Mail Stop 0505, BENTONVILLE, AR 72716, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
WALMART INC. (Owner Number: 2316750)
Owner / Operator Contact Address
811 Excellence Drive, Mail Stop 0505, Bentonville, AR 72716, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

VisualEYEz

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HLG Pupillometer, Ac-Powered Ophthalmic Class 1 886.1700 2024-08-30

Official Correspondent

Heather Sevak

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

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

Other Registrations for Same Entity

Registration Number Establishment Name Location
3005890070 Walmart Optical Lab Dallas, TX, US
3003512352 Wal-Mart Optical Lab Fayetteville, AR, US
3010119835 Wal-Mart Optical Lab #9065 Crawfordsville, IN, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 2316750. Last updated year: 2026. Please use registration number 2316750 when referencing this establishment in official correspondence.
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