ABOUT
HISTORY
2000
- APR : Establish of legal company
- May : Venture company technology
registration approval
2001
- Mar : Laboratory registered
- May : Begin of Stent study
- JUN : Capital increase
2002
- JUN : Chief executive officer change
- Dec : Moved company to Jayang-dong
2003
- JAN : Factory registration
- Aug : Venture company,
Laboratory approval
2008
-JUL : CE approval (Extension)
EGIS Biliary/Pyloric/Colorectal stent)
-Sep : TAA overseas technology license
2011
-JAN : Product manufacturing license acquired
-Mar : CE approval (EGIS Esophageal Stent
/Guide Wire/Micro Catheter)
- May : Vietnamese plant begins operation
- Oct : Dealership contracts in Russia, Belgium,
Czech, Vietnam, Philippines, Saudi
2012
- Feb : CE approval
- Aug : HQ moves to Seongnam
- Sep : KFDA approval
- Oct : Dealership contracts in Malaysia,
Spain, Estonia, Croatia, Indonesia
2013
-JAN∼Dec : KFDA approval
-Feb : China SFDA product registration
ISO 13485 approval: Class III Seal
-APR : New product launches in Russia
-Aug : Additional CE approval
(Microcatehter & Guide Wire)
-Dec : Japanese PMDA product registration
- JAN-Dec : Worldwide product registration
2014
- JAN∼Mar : Japanese QMS audit
and product launch
- Mar : CE extension review
- APR : China SFDA registration underway
2017
-JUL : Completed S&G Head Office Building
in Yongin city
