Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042972690

FEI Number

3042972690

Entity Name

MAJUTECH INC.

City/State/Country

Geumcheon-gu Seoul, KR

Establishment Address

#1404, World Meridian 2-cha, 123, Gasan digital 2-ro, Geumcheon-gu Seoul 08505, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MAJUTECH Inc. (Owner Number: 10094851)

Owner / Operator Contact Address

#1404, World Meridian 2-cha, 123, Gasan digital 2-ro, Geumcheon-gu, KR-11 08505, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VeinVu (models: VeinVu 200, VeinVu 100+)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KZA	Device, Vein Location, Liquid Crystal	General Hospital	Class 1	880.6970	2025-12-29

Official Correspondent

NOWOONG KWAK

US Agent Details

Jung Ryun Ahn Business: KMC USA, Inc Email: kmc.usa@kmcerti.com Phone: (646) 3576058

Related Public Records

Same Entity

MAJUTECH Inc.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042972690. Last updated year: 2026. Please use registration number 3042972690 when referencing this establishment in official correspondence.