Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009780106

FEI Number

3009780106

Entity Name

ID EYEWEAR

City/State/Country

Hong Kong, HK

Establishment Address

19/F, LEE GARDEN ONE, 33 HYSAN AVENUE, CAUSEWAY BAY,, Hong Kong N/A, HK

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Export Device to the United States But Perform No Other Operation on Device,Develop Specifications But Do Not Manufacture At This Facility,Manufacture Medical Device

Owner / Operator

ID Eyewear (Owner Number: 10044157)

Owner / Operator Contact Address

5/F MANULIFE PLACE, 348 KWUN TONG ROAD, KOWLOON, Hong Kong, HK-NOTA 852, HK

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ID eyewear

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2013-05-08

Official Correspondent

Alex Tse

US Agent Details

Daryl Williams Business: MODO Eyewear Email: dwilliams@modo.com Phone: (212) 9654922

Related Public Records

Same Entity

ID Eyewear

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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3009554831	ROGER EYE DESIGN	Etten-Leur Noord-Brabant, NL
3013507321	DEM FACTORY S.R.L.	Limana Belluno, IT
3015243992	L.G.R SRL	Roma, IT

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009780106. Last updated year: 2026. Please use registration number 3009780106 when referencing this establishment in official correspondence.