CG MedTech Corporation - Driving beyond the innovations

History

Approved by FDA for CBT Screw Fixation System 작성자 : 관리자 (IP: *.9.5.5) 작성일 : 2019-07-17 10:09 읽음 : 1,970

2024
- 11 Change of company name : CG MedTech
- 04 Approved by FDA for UniSpace® Stand-Alone C Cage
- 04 Approved by Korea MFDS for UniSpace® Stand-Alone C Cage
- 02 Approved by FDA for INNOVERSE™ Spinal System
- 02 Approved by Korea MFDS for INNOVERSE™ Spinal System
2022
- 06 Change of company name : innosys
- 05 Start of gel-type mask pack maker and nourisher business
- 05 Contract to purchase battery cell with LGES
- 03 Change of company name : Edisoninno
2021
- 04 Acquired ANVISA for Velofix SA Ti CAGE
2020
- 11 Acquired CE for ANAX™ 5.5 Spinal Systems including 8 items
- 04 Acquisition of Infinity Works
2019
- 08 Acquried COFEPRIS for Velofix SA Cervical CAGE and TLIF CAGE
- 07 Approved by FDA for VELOFIX TLIF CAGE
- 05 Acquried ANVISA for VELOFIX TLIF CAGE
- 04 Acquired MFDS for ASPIRON S
- 03 Approved by Japan MHLW for L'DISQ PLASMAX
2018
- 12 Approved by Korea MFDS for Polarfix™ Facet Screw System
- 12 Approved by FDA for CBT Screw Fixation System
- 12 Approved by FDA for ANAX OCT Spinal System FDA
- 09 Approved by FDA for SECULOK™ ACP System
- 08 Cleared by CE for resomet Bioresorbable Metal
- 07 Cleared by CE for Benefix Interspinous Fixation System
- 04 Cleared by CE for PLASMAX
- 01 Approved by FDA for Polarix Facet Screw Fixation System
2017
- 12 Approved by FDA for Velofix™ TLIF Cage
- 12 Acquisition of DM Power co., Ltd
- 11 Approved by FDA for Velofix SA Cervical Cage
- 08 Signed a distributor contract for Microport's Cardiovascular Stent
- 07 Approved by FDA for Velofix™ Interbody Fusion System
- 05 Approved by MFDS for Resomet Suture Anchor
- 02 Approved by MFDS for Resomet Interference screw
- 01 Signed a distributor contract for bone substitution product of Wright Medical Group
2016
- 03 Approved by MFDS for K-Wire, Pin Biodegradable (Bioresorbable MgCa Alloy Metal)
- 02 Approved by COFEPRIS, Mexico for L'disQ
- 01 Approved by ANVISA, Brazil for L'disQ
2015
- 11 Enlisted at Korea Stock Exchange (KOSDAQ)
- 04 Approved by MFDS for Orthopaedic Bone Screw, Biodegradable (Bioresorbable MgCa Alloy Metal)
2014
- 12 Awarded by World Intellectual Property Organization
- 03 Cleared by FDA 510(K) for Velofix™ PEEK Cage (Cervical, Lumbar)
2013
- 12 Cleared by FDA 510(K) for Perfix™ Iliac Screw system
- 11 Cleared by FDA 510(K) for ANAX 5.5™ Spinal System
- 08 Cleared by FDA 510(K) for Aspiron™ ACP System
- 08 Launched L’DISQ C.7
2012
- 07 Established a U.S. Branch Office
- 05 Cleared by CE Marking for L’DISQ C
- 05 Cleared by FDA 510(K) for Dyna Locking Ankle Nail
- 05 Launched L’DISQ C
- 01 Cleared by FDA 510(K) for Dyna Locking Cannulated Screw
2011
- 12 Launched Perfix MIS System
- 11 Launched Perfix Iliac Screw System
- 09 Cleared by CE Marking for Perfix Iliac Screw System
- 02 Launched Neo IC Peek Cervical Cage
2010
- 12 Cleared by FDA 510(K) for OtiGen Total Knee System
- 11 Cleared by CE Marking for Neo IC Peek Cervical Cage
- 08 Launched Neo IC Peek Lumbar Cage
- 06 Cleared by FDA 510(K) for Dyna Locking Trochanteric Nail
- 06 Cleared by CE Marking for Neo IC Peek Lumbar Cage
2009
- 11 Launched L’DISQ
- 11 Cleared by FDA 510(K) for Dyna Locking IM Nail
- 11 Cleared by FDA 510(K) for Perfix Spinal System
- 07 Cleared by CE Marking for Perfix Spinal System
- 06 Launched Perfix Spinal System in domestic market
- 05 Launched OPTIMA Transition Screw in domestic market
- 05 Cleared by CE Marking for L’DISQ
- 04 Cleared by CE for OPTIMA ZS Transition Screw
- 01 Launched Dyna Locking Telescopic Nail in domestic market
2008
- 07 Launched DREAM PLIF PEEK Cage in domestic market
- 03 Launched Dyna Locking Ankle Nail
2007
- 10 Launched BAE Offset HTO Plate in domestic market
- 10 Cleared by FDA 510(K) for the OPTIMA ZS Transition Screw
- 03 Launched the Dyna Locking Trochanteric Nail in domestic market
- 01 Launched the Periacetabular Osteotomy in domestic market
2005
- 11 Entered into Exclusive Distributorship Agreement OPTIMA, HOOK & OTS with Zimmer Spine.
- 09 Cleared by FDA 510(K) for the MAXIMA
2003
- 11 Awarded Five Million Dollar Export Company form MOCIE
2002
- 06 Cleared by FDA 510(K) for the OPTIMA
2001
- 11 Awarded Million Dollar Export Company form MOCIE
- 11 Designated as INNO-BIZ company from SMBA
2000
- 10 Cleared by FDA 510(K) for the GSFS
- 10 Moved to a new factory located at Younghyun Industrial Complex
- 07 Renamed as U&I Corporation
- 04 Designated as a Venture Company from SMBA, a High-tech Company from KTCGF
1999
- 10 Launched the GSFS in the domestic market
- 09 Acquired EN46001/ISO9001 Quality System Approval
1997
- 09 Incorporated as DKM Co., Ltd.
1993
- 09 Company Established & Introduced ‘Ring External Fixator’ [Ominifixator] in the market

About CG MedTech	Product	Quality Management	Contact us	CG MedTech Corp.
CG MedTech Corporation	resomet	Quality Policy	Inquiry receipt	1, Sangwon 12-gil, Seongdong-gu,
History	Spine	Patent	CG MedTech Corporation Headquarter	Seoul, Republic of Korea
Global Network	Trauma	Certificate	CG MedTech Seoul R&BD Center	Tel. +82 31 860 6800
	Pain Management		CG MedTech US Branch	Fax. +82 31 852 0107

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