Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010391227

FEI Number

3010391227

Entity Name

W-MEDICAL

City/State/Country

Namyangju-si Gyeonggi, KR

Establishment Address

4F, 402, Byeollae 3-ro, Namyangju-si Gyeonggi 12097, KR

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device,Manufacture Medical Device

Owner / Operator

W-Medical (Owner Number: 10044683)

Owner / Operator Contact Address

F4, 402, Byeollae 3-ro, Namyangju-si, KR-41 12097, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

MiracleWave Plus The Miracle wave HP50 The Miracle wave Shockwave F1 The Miracle wave Handywave

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2013-07-15

Official Correspondent

No official correspondent registered.

US Agent Details

JEAHWAN SON Business: CL MEDIX INC Email: clmedixinc@gmail.com Phone: (847) 6566795

Related Public Records

Same Entity

W-Medical

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

View Entity Profile →

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3030407739	CL MEDIX INC	Chantilly, VA, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010391227. Last updated year: 2026. Please use registration number 3010391227 when referencing this establishment in official correspondence.