Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008727534

FEI Number

3008727534

Entity Name

Aristar Company Ltd, China Factory

City/State/Country

Dongguan City Guangdong, CN

Establishment Address

Lu Cun Zone, Gao Bu Town, Dongguan City Guangdong PRC, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Aristar Company Ltd China Factory (Owner Number: 10034532)

Owner / Operator Contact Address

Lu Cun Zone, Gao Bu Town, Dongguan City, CN-GD PRC, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Aristar

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQZ	Frame, Spectacle	Ophthalmic	Class 1	886.5842	2010-12-09

Official Correspondent

Douglas Fryer

US Agent Details

Douglas Fryer Business: Charmant USA Email: dfryer@charmant.com Phone: (973) 5381511

Related Public Records

Same Entity

Aristar Company Ltd China Factory

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 3008727534. Last updated year: 2026. Please use registration number 3008727534 when referencing this establishment in official correspondence.