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KIM JONG SOOK

DAEJU MEDITECH ENGINEERING CO.,LTD.

808nm Diode Laser for hair removal Laser, Co2 Fractional Laser, HIFU for skin lifting & tightening

DAEJU MEDITECH ENGINEERING CO., LTD. is an aesthetic medical device manufacturing company providing optimum quality products including all services not only internally in Korea, but throughout Japan, Southeast Asia, Middle East, Europe, Australia, and other countries. we that leads exports to more than 40 countries with own technology have accumulated know-how in technology development, manufacturing, export, and maintenance etc. with more than 15 years of experience. As the result, we have gained satisfactory trust from customers until now. For your references, our medical devices have been certified with KFDA, TGA, CE, TFDA, GOST, ANVISA approvals and our aesthetic devices have been certified with KC approval in Korea. We are manufacturing the Aesthetic Medical & Beauty Device products as follows; ⓐQ-S/W Nd YAG laser(ACTIVO), ⓑ4 types of HIFU devices(cartridge type HIFU: HIPRO and HIPRO-S / one handpiece type HIFU: HIPRO-V / home care type HIFU: HIPRO-Q), ⓒ808nm diode laser for hair removal(AROMA GRAND), ⓓCO2 Fractional Laser for skin rejuvenation(PENTAGON GRAND), ⓔ405nm & 635nm Diode laser for Onychomycosis treatment(TINEA), ⓕUltrasound Local Dynamic Micro-Massage device for crystal shining skin(HIPRO-L).

▶ Feb. 2006: Establish a company DAEJU MEDITECH ENGINEERING
▶ Oct. 2007: License for medical manufacturing by KFDA
▶ Mar. 2008: Laser surgical apparatus approved by KFDA(PENTAGON)
▶ Jul. 2008: Certificate of KGMP by KFDA
▶ Feb. 2010: Laser surgical apparatus approved by KFDA(AROMA)
▶ Jun. 2011: Certificate of CE Laser surgical apparatus by ITC
(AROMA GRAND, PENTAGON GRAND)
▶ May. 2012: Laser surgical apparatus approved by KFDA(PENTAGON GRAND)
▶ Jan. 2013: Certificate of EN ISO 13485:2012 by ITC
▶ Jun. 2014: High intensity focused Ultrasound surgical unit approved by KFDA(HIPRO)
▶ May. 2015: Transition of corporation DAEJU MEDITECH ENGINEERING CO., LTD.
▶ Oct. 2016: Certificate of CE by KIWA(HIPRO)
Certificate of EN ISO 13485:2016 by LL-C
▶ Dec. 2016: Registration of patent(by Korean Intellectual Property Office)
▶ Apr. 2019: Certificate of CE by MTIC(AROMA GRAND)
▶ Dec. 2019: HIFU approved by TGA(HIPRO)
▶ Jan. 2020: Renewal of EU Representative Contract
(AROMA GRAND, PENTAGON GRAND, HIPRO)
▶ Feb. 2020: Nd’Yag Laser approved by KFDA(ACTIVO)
▶ Feb. 2020: Change of Factory
(#501-504, HausD Sejong Tower, 26, Seongsu-il-ro 10-gil, Seongdong-gu,Seoul, Korea)
▶ Nov. 2020: Laser surgical unit, diode approved by GOST(AROMA GRAND)
▶ Dec. 2020: Registration of patent (by Korean Intellectual Property Office)
▶ Feb. 2021: Certificate of CE by MTIC (PENTAGON GRAND)
▶ Apr. 2021: Diode Laser unit approved by KFDA(AROMA GRAND)
Renewal Certificate of CE by KIWA(HIPRO)
▶ Aug. 2021: Medical Laser Irradiation System approved by KFDA(ATOM Laser)

KIMES 2019
IMCAS ASIA 2019
Cosmobeauty Malaysia 2019
Consumer Goods Showcase Korea 2019
Intercharm UKRAINE 2019
MEDICA Germany 2019
Cosmoprof 2019 in Hong Kong
Arab Health Dubai 2020
KIMES 2020
Beauty World JAPAN 2020
KIMES 2021, KOREA
Global Business Sourcing Fair 2021, KOREA
PHARMEDI 2021, VIETNAM
Intercharm 2021, Korea
MEDICA 2021, GERMANY
ASEAN & INDIA Business Week 2021
SBA TRADE WEEK 2021, KOREA
Medipharm EXPO 2021, VIETNAM

Certificate of EN ISO 13485:2016
Certificate of CE by MTIC(AROMA GRAND)
Certificate of CE by MTIC (PENTAGON GRAND)
Certificate of CE by KIWA (HIPRO)