Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030970133

FEI Number

3030970133

Entity Name

K1MEDGLOBAL Co., Ltd.

City/State/Country

Seoul, KR

Establishment Address

1006, 1008, 1009, Woolim e-biz center II, 12, Digital-ro 33gil, Guro-gu, Seoul 08377, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

K1MEDGLOBAL Co., Ltd. (Owner Number: 10090497)

Owner / Operator Contact Address

1006, 1008, 1009, Woolim e-biz center II, 12, Digital-ro 33gil, Guro-gu, KR-11 08377, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K222400

PMA Number

N/A

All Registered Proprietary Names

MAGTUNE (MST-1001) COREVEX (MST-1002) COREVEX S (CSS-4002)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	Class 2	890.5850	2024-04-04

Official Correspondent

YounSoo Nam

US Agent Details

David Hyun Jun Paek Email: dpaek.rennes@gmail.com Phone: (818) 9030660

Related Public Records

Same Entity

K1MEDGLOBAL 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
K221200	Xbody Hungary Kft.	XBody Go USA, XBody Pro USA	2023-01-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3030970133. Last updated year: 2026. Please use registration number 3030970133 when referencing this establishment in official correspondence.