Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003512352

FEI Number

3003512352

Entity Name

Wal-Mart Optical Lab

City/State/Country

Fayetteville, AR, US

Establishment Address

2314 W. Martin Luther King Jr. Blvd., Fayetteville, AR 72701, US

Establishment Type(s)

Repack or Relabel Medical Device,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

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

PRIVATE LABEL Private label

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2013-12-30
NJH	Lens, Spectacle (Prescription), For Reading Discomfort	Ophthalmic	Class 1	886.5844	2013-12-30

Official Correspondent

No official correspondent registered.

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
3010119835	Wal-Mart Optical Lab #9065	Crawfordsville, IN, US
2316750	WALMART INC.	BENTONVILLE, AR, US

Similar Registrations

Registration Number	Establishment Name	Location
3006755718	DONGGUAN YUEHENG OPTICAL CO. LTD.	Dongguan Guangdong, CN
3015534032	BOLLE SAFETY INC	Carlsbad, CA, US
3007675955	Carl Zeiss Vision Canada, Inc.	Toronto Ontario, CA
1000428458	GKB OPHTHALMICS LIMITED - UNIT II	North Goa Goa, IN
3038136215	MEIVISION (VIETNAM) CO., LTD	Ho Chi Minh City, VN

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3003512352. Last updated year: 2026. Please use registration number 3003512352 when referencing this establishment in official correspondence.