Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3040138099

FEI Number

3040138099

Entity Name

HAHO MEDI

City/State/Country

Wonju-si Gangwon, KR

Establishment Address

1003, 200, Gieopdosi-ro, Jijeong-myeon, Wonju-si Gangwon 26354, KR

Establishment Type(s)

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

Owner / Operator

HAHO MEDI (Owner Number: 10093840)

Owner / Operator Contact Address

1003, 200, Gieopdosi-ro, Jijeong-myeon, Wonju-si, KR-42 26354, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

#OOTD Derma Expert Pro HA-CAREME2024 mixsoon Derma Booster PRO

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	2025-08-04

Official Correspondent

Hayoung Kim

US Agent Details

Daniel Hwang Email: Regulatoryaffairs@jnmglobal.net Phone: (302) 2018886

Related Public Records

Same Entity

HAHO MEDI

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 3040138099. Last updated year: 2026. Please use registration number 3040138099 when referencing this establishment in official correspondence.