Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010890287

FEI Number

3010890287

Entity Name

MAXSTAR INDUSTRIAL CO LTD

City/State/Country

Gimpo Gyeonggi, KR

Establishment Address

152-12 Hwanggeum-ro 23beon-gil, Yangchon-eup, Gimpo Gyeonggi 415843, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Maxstar Industrial Co., Ltd. (Owner Number: 10046491)

Owner / Operator Contact Address

152-12 Hwanggeum-ro 23beon-gil, Yangchon-eup, Gimpo, KR-41 10048, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K211460

PMA Number

N/A

All Registered Proprietary Names

AIR RELAX MODEL UAM-8100, UAM-8100N HAMMERZ, Model: HM-1 UAM-8100 AIR RELAX PRO MODEL AR-4 AIR RELAX MODEL AR-1 & MODEL AR-2 Air Relax Plus Model AR-3

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
IRP	Massager, Powered Inflatable Tube	Physical Medicine	Class 2	890.5650	2019-06-06
ISA	Massager, Therapeutic, Electric	Physical Medicine	Class 1	890.5660	2019-10-15
IRP	Massager, Powered Inflatable Tube	Physical Medicine	Class 2	890.5650	2014-03-28
IRP	Massager, Powered Inflatable Tube	Physical Medicine	Class 2	890.5650	2021-10-05
IRP	Massager, Powered Inflatable Tube	Physical Medicine	Class 2	890.5650	2021-03-17
IRP	Massager, Powered Inflatable Tube	Physical Medicine	Class 2	890.5650	2021-06-17

Official Correspondent

John Kim

US Agent Details

BEOMJOON LEE Business: DIODE ART ENGINEERING DBA AIR RELAX Email: sales@air-relax.com Phone: (323) 2854231

Related Public Records

Same Entity

Maxstar Industrial 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
K242140	Jiale Health Technology Shenzhen Co., Ltd.	Air Compression Leg Massager (K-705)	2025-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010890287. Last updated year: 2026. Please use registration number 3010890287 when referencing this establishment in official correspondence.