Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009981789

FEI Number

3009981789

Entity Name

SHENZHEN HUIMING OPTICAL CO.,LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

NO.4, Xihu Industrial, Xikeng Cun, Henggang street, Longgang District, Shenzhen Guangdong 518115, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Shenzhen Huiming Optical Co.,Ltd (Owner Number: 10047749)

Owner / Operator Contact Address

NO.4, Xihu Industrial, Xikeng Cun, Henggang street, Longgang District, 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

Lens, spectacle (prescription), for reading discomfort Lens, spectacle, non-custom (prescription) Frame, spectacle Shield, eye, ophthalmic (including sunlamp protective eyewear and post-mydriatic eyewear)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NJH	Lens, Spectacle (Prescription), For Reading Discomfort	Ophthalmic	Class 1	886.5844	2014-10-27
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2014-10-27
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2014-10-27
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2020-03-26

Official Correspondent

No official correspondent registered.

US Agent Details

shally dream Email: mljyangguang@msn.com Phone: (909) 2820679

Related Public Records

Same Entity

Shenzhen Huiming Optical Co.,Ltd

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
K910951	United Optical, Spa	OPTHLAMIC FRAMES	1991-05-06

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009981789. Last updated year: 2026. Please use registration number 3009981789 when referencing this establishment in official correspondence.