2022
12
-
Packaging Validation Completed
11
-
KS P ISO 13485:2016 Medical device quality management system process certification
10
09
-
Product U.S. FDA Registration(Product Code KIZ, 510K Exempt ,Class 1, Certificate No. IRC-NF-202210)
-
Clean Room Validation Completed
-
Daegu Headquarters Sterilization Validation(in progress)
08
-
Establishment of KGMP-class facilities at Daegu Headquarters
06
-
Selection of TIPS Operation Support Project(CCEI.CREATIVEKOREA)
-
TIPS Selection
04
-
Selection of consulting support projects for commercialization of the health industry (licensing for production)(KHIDI)
-
Attracting investment from joint technology holding companies in Daegyeong area
2021
07
-
Selection of medical device convergence utility project based on intelligent machine(GIBF)
06
-
Quality Management System Certification (KS Q ISO 9001:2015/ISO 9001:2015)
-
Selection of Startup Leap Package selection(KHIDI)
2020
12
-
Selection of technology transfer commercialization business(INNOPOLIS)
-
Initial Start-up Package Selection(KHIDI)
11
-
Venture Business Certification(KIBO)
-
Selected for U-TECH Enterprise
-
Accreditation evaluation of excellent technology companies(KIBO)
2018-2019
2019
11
-
Establishment of a research institute affiliated with a company
2018
03
-
Establishment of corporate research institute
-
Lab Enterprise Registration
02
-
Establishment of a corporation