Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013091260

FEI Number

3013091260

Entity Name

WENZHOU FAITH IMPORT & EXPORT CO. LTD.

City/State/Country

Wenzhou Zhejiang, CN

Establishment Address

7th, Alfa Mansion, XINCHENG RD, Wenzhou Zhejiang 325000, CN

Establishment Type(s)

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

Owner / Operator

Wenzhou Faith Import & Export Co. Ltd. (Owner Number: 10052889)

Owner / Operator Contact Address

7th, Alfa Mansion, Xincheng Rd, Wenzhou, CN-ZJ 325000, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SPECTACLE, MAGNIFYING Lens, spectacle, noncustom (prescription) RGD-120 Magnifying Glasses Magnifier

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2016-10-19
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2016-10-19
HJF	Magnifier, Hand-Held, Low-Vision	Ophthalmic	Class 1	886.5540	2023-05-19

Official Correspondent

HONGTU ZHANG

US Agent Details

FDAIMPORTS.COM LLC Email: registration@fdaimports.com Phone: (410) 2202800

Related Public Records

Same Entity

Wenzhou Faith Import & Export Co. Ltd.

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

View Entity Profile →

Similar Registrations

Registration Number	Establishment Name	Location
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 3013091260. Last updated year: 2026. Please use registration number 3013091260 when referencing this establishment in official correspondence.