Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010508185

FEI Number

3010508185

Entity Name

UPDATE OPTICAL MANUFACTURER LIMITED

City/State/Country

Longgang District, Shenzhen City Guangdong, CN

Establishment Address

2F No.26-1 Baolong Road, Dakang Community, Henggang Sub-district, Longgang District, Shenzhen City Guangdong 518115, CN

Establishment Type(s)

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

Owner / Operator

Update Optical Manufacturer Limited (Owner Number: 10045095)

Owner / Operator Contact Address

2F No.26-1 Baolong Road, Dakang Community, Henggang Sub-district, LongGang District, Shenzhen City, 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 Frame

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2013-10-21

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: REGISTRAR CORP Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

Update Optical Manufacturer Limited

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 3010508185. Last updated year: 2026. Please use registration number 3010508185 when referencing this establishment in official correspondence.