Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3005290074

FEI Number

3005290074

Entity Name

EssilorLuxottica (Jiangsu) Optical Manufacturing Co., Ltd.

City/State/Country

Danyang Jiangsu, CN

Establishment Address

Optical Industrial Park, Situ Town, Danyang Jiangsu 212331, CN

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

EssilorLuxottica (Jiangsu) Optical Manufacturing Co., Ltd. (Owner Number: 10039752)

Owner / Operator Contact Address

Optical Industrial Park, Situ Town, Danyang, CN-JS 212331, 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	2012-02-07
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2018-12-06
HQG	Lens, Spectacle, Non-Custom (Prescription)	Ophthalmic	Class 1	886.5844	2012-02-07

Official Correspondent

No official correspondent registered.

US Agent Details

Jessie Yao Email: info@medright-tech.com Phone: (718) 2169957

Related Public Records

Same Entity

EssilorLuxottica (Jiangsu) Optical Manufacturing 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 3005290074. Last updated year: 2026. Please use registration number 3005290074 when referencing this establishment in official correspondence.