Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013688041

FEI Number

3013688041

Entity Name

AOKER EYEWEAR MANUFACTORY LIMITED

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

Xiandong,SiLian Industrial, HengGang, LongGang, Shenzhen Guangdong 518115, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

AOKER EYEWEAR MANUFACTORY LIMITED (Owner Number: 10055233)

Owner / Operator Contact Address

Xiandong,SiLian Industrial, HengGang, LongGang, Shenzhen, CN-GD 518115, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Sunglasses Magnifying Spectacle Reading Glasses Spectacle Frame

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQY	Sunglasses (Non-Prescription Including Photosensitive)	Ophthalmic	Class 1	886.5850	2020-03-08
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2020-03-08
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2020-03-08

Official Correspondent

Micro Zhang

US Agent Details

Wei Huang Email: weihuang1979@gmail.com Phone: (713) 5053208

Related Public Records

Same Entity

AOKER EYEWEAR MANUFACTORY LIMITED

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K940726	Jay-Y Enterprises Co., Inc.	NONE-GENERIC	1994-04-11
K934837	Simon Marketing, Inc.	SUNGLASSES	1993-12-08
K852902	Yours Enterprise Co., Ltd.	METALLIC SUNGLASSES	1985-08-12
K970895	Custom Optical Frames, Inc.	CUSTOM OPTICAL SUNGLASS FRAMES	1997-05-06
K853921	Winsburn Company , Ltd.	ALL KINDS OF SUNGLASSES	1985-10-15

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3009141079	STAGE	Sandy, UT, US
3013857947	FARFETCH ITALIA S.R.L.	MILAN Milano, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013688041. Last updated year: 2026. Please use registration number 3013688041 when referencing this establishment in official correspondence.