Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3032010300

FEI Number

3032010300

Entity Name

TIANJIN MASTERVISION TECHNOLOGY CO., LTD.

City/State/Country

Wuqing District Tianjin, CN

Establishment Address

1st Floor No.15 Building. No. 89 Heyuan Road, Jing-jin Technology Valley, Wuqing District Tianjin 301700, CN

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Tianjin MasterVision Technology Co., Ltd. (Owner Number: 10092434)

Owner / Operator Contact Address

1st Floor No.15 Building. No. 89 Heyuan Road, Jing-jin Technology Valley, Wuqing District, CN-TJ 301700, CN

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K241398

PMA Number

N/A

All Registered Proprietary Names

EyeSpace Scleral EyeSpace Bespoke SDJMASTERVISION

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HQD	Lens, Contact (Other Material) - Daily	Ophthalmic	Class 2	886.5916	2025-01-07

Official Correspondent

Delia Ke

US Agent Details

Bret Andre Business: EYEREG CONSULTING INC. Email: bandre@fdapproval.com Phone: (503) 3725226

Related Public Records

Same Entity

Tianjin MasterVision Technology 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
K963512	Benz Research and Development Corp.	BENZ B17 (KOLFOCON A) RIGID GAS PERMEABLE (HYDROPHOBIC DAILY WEAR CONTACT LENS (CLEAR AND TINTED, LATHE-CUT FROM LENS BL	1997-07-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3032010300. Last updated year: 2026. Please use registration number 3032010300 when referencing this establishment in official correspondence.