Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3018502801

FEI Number

3018502801

Entity Name

GHL CO., LTD.

City/State/Country

Namyangju-si Gyeonggi, KR

Establishment Address

6, Jinbeol-ro 119beon-gil, Jinjeop-eup, Namyangju-si Gyeonggi 12021, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GHL Co., Ltd. (Owner Number: 10095031)

Owner / Operator Contact Address

6, Jinbeol-ro 119beon-gil, Jinjeop-eup, Namyangju-si, KR-41 12021, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

GOG QIE-300

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	2026-01-16
IRT	Pad, Heating, Powered	Physical Medicine	Class 2	890.5740	2026-01-16

Official Correspondent

Ki Young Shin

US Agent Details

Ki Soo Kim Business: FKS Bio Science Email: fksbio02@gmail.com Phone: (213) 9999805

Related Public Records

Same Entity

GHL Co., Ltd.

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K881862	Thermo Body Wrap Systems, Inc.	THERMO-BODY-WRAP SYSTEM	1988-10-13

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3018502801. Last updated year: 2026. Please use registration number 3018502801 when referencing this establishment in official correspondence.