Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3020750249

FEI Number

3020750249

Entity Name

WITHNIX CO., LTD.

City/State/Country

Gwangju, KR

Establishment Address

Munhyung-ri 593-14 Opo-ro, Opo-eup, Gwangju 12774, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

WITHNIX CO., LTD. (Owner Number: 10094285)

Owner / Operator Contact Address

Munhyung-ri 593-14 Opo-ro, Opo-eup, Gwangju, KR-29 12774, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Centellian24 MADECA PRIME MAX Centellian24 MADECA PRIME RITUAL WHITE PEARL DERMAURA CORE DERMAURA 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	2025-11-21

Official Correspondent

Yoonseong Shin

US Agent Details

Wonpyo Hong Business: Wonpyo Hong Email: dean.baek@comvalis-usagent.com Phone: (415) 9809460

Related Public Records

Same Entity

WITHNIX 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 3020750249. Last updated year: 2026. Please use registration number 3020750249 when referencing this establishment in official correspondence.