Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3003976094

FEI Number

3003976094

Entity Name

Createch Industrial (Shen Zhen) Limited

City/State/Country

BAO AN, SHENZHEN Guangdong, CN

Establishment Address

SECTION F.,3RD INDUSTRIAL ZONE, GONG HE CUN, SHA JING, BAO AN, SHENZHEN Guangdong 518104, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

CREATECH INDUSTRIAL LIMITED (Owner Number: 9048614)

Owner / Operator Contact Address

FLAT 2, 1/F, BLOCK 2, WAH FUNG IND. CTR., 33-39 KWAI FUNG CRESCENT,, KWAI CHUNG,, HK-NOTA --, HK

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	2005-10-12

Official Correspondent

LEO CHAN

US Agent Details

Kevin Walls Email: kevin@reginsight.com Phone: (720) 9625412

Related Public Records

Same Entity

CREATECH INDUSTRIAL 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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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 3003976094. Last updated year: 2026. Please use registration number 3003976094 when referencing this establishment in official correspondence.