Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013151253

FEI Number

3013151253

Entity Name

JIANGSU YOULI OPTICS SPECTACLES CO., LTD.

City/State/Country

Danyang Jiangsu, CN

Establishment Address

No.18 South to Reservoir, Yiwei Road, Economic Development Zone, Danyang Jiangsu 212300, CN

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

Jiangsu Youli Optics Spectacles Co., Ltd. (Owner Number: 10056597)

Owner / Operator Contact Address

No.18 South to Reservoir, Yiwei Road, Economic Development Zone, Danyang, CN-JS 212300, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2017-12-23
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2017-12-23

Official Correspondent

Thomas Pang

US Agent Details

Thomas Pang Business: kapo optik Email: kapo_optik@yahoo.com Phone: (626) 2266699

Related Public Records

Same Entity

Jiangsu Youli Optics Spectacles 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

Similar Registrations

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3013956081	RENEE'S READERS	New City, NY, US
3026270768	ASIASTAR INDUSTRY(HUIZHOU)CO., LTD	Huizhou City Guangdong, CN
3000180670	Dongguan Rijinyuehui Optical Co.,Ltd	Dongguan Guangdong, CN
3009206998	WORLDWIDE PACKAGING, INC	Livermore, CA, US
3013009176	HYUNDAI SAFETYWEAR CO.	Tainan City, TW

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013151253. Last updated year: 2026. Please use registration number 3013151253 when referencing this establishment in official correspondence.