Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016856167

FEI Number

3016856167

Entity Name

SHENZHEN BAOJIE OPTICAL CO., LTD

City/State/Country

Shenzhen Guangdong, CN

Establishment Address

101/201/301, Building C, No.5 Liangyun street, Anliang Henggang Sub-district , Longgang District, Shenzhen Guangdong 518115, CN

Establishment Type(s)

Repack or Relabel Medical Device,Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

SHENZHEN BAOJIE OPTICAL CO., LTD (Owner Number: 10092098)

Owner / Operator Contact Address

101/201/301, Building C, No.5 Liangyun street, Anliang Henggang Sub-district , 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

Spectacle , Magnifying, Frame, Optical frame Reading glasses Protective glasses, Safety Goggles

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2024-12-04
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2024-12-04
HOY	Shield, Eye, Ophthalmic (Including Sunlamp Protective Eyewear And Post-Mydriatic Eyewear)	Ophthalmic	Class 1	886.4750	2024-12-04

Official Correspondent

SHUTAO TAN

US Agent Details

Yueting Zhu Business: SOUTH BAY INNOVATION LLC Email: southbayinnovation@southbayinnovation.com Phone: (424) 3769142

Related Public Records

Same Entity

SHENZHEN BAOJIE 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 3016856167. Last updated year: 2026. Please use registration number 3016856167 when referencing this establishment in official correspondence.