Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016603270

FEI Number

3016603270

Entity Name

SKINREX CO., LTD.

City/State/Country

Seongnam-si Gyeonggi, KR

Establishment Address

112 Sagimakgol-ro, Jungwon-gu, Seongnam-si Gyeonggi 13207, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

SKINREX CO., LTD. (Owner Number: 10090476)

Owner / Operator Contact Address

112 Sagimakgol-ro, Jungwon-gu, Seongnam-si, KR-41 13207, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

SKNLAB CLV-1000 SKNLAB SKNBAR

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
GFE	Brush, Dermabrasion, Powered	General, Plastic Surgery	Class 1	878.4820	2024-06-04
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2024-04-02

Official Correspondent

No official correspondent registered.

US Agent Details

UJU Krallum Business: Onbix Corp US Email: ONBIXUS@GMAIL.COM Phone: (843) 5828036

Related Public Records

Same Entity

SKINREX CO., LTD.

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

View Entity Profile →

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3005450640	EUNSUNG GLOBAL CORP.	Wonju-si Gangwon, KR
3012616488	BRERA MEDICAL INCORPORATED	Northborough, MA, US
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3016603270. Last updated year: 2026. Please use registration number 3016603270 when referencing this establishment in official correspondence.