Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3039388306

FEI Number

3039388306

Entity Name

JION MEDITECH CO.LTD

City/State/Country

Anyang-si Gyeonggi, KR

Establishment Address

12-18, Simin-daero 327beon-gil, Dongan-gu, Anyang-si Gyeonggi 14056, KR

Establishment Type(s)

Repack or Relabel Medical Device,Manufacture Medical Device,Foreign Private Label Distributor

Owner / Operator

JION MEDITECH Co.Ltd (Owner Number: 10093749)

Owner / Operator Contact Address

12-18, Simin-daero 327beon-gil, Dongan-gu, Anyang-si, KR-41 14056, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Dualsonic Professional Gold Dualsonic Maximum Dualsonic Professional Alpha Dualsonic Fit Up Belt Dualsonic Effect Dualsonic Alto

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	2025-07-02

Official Correspondent

Kate Kim

US Agent Details

Drew Ye Email: kcosrp.us@gmail.com Phone: (323) 7491964

Related Public Records

Same Entity

JION MEDITECH Co.Ltd

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 3039388306. Last updated year: 2026. Please use registration number 3039388306 when referencing this establishment in official correspondence.