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2022

함께 상단에

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, Packaging 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

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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

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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

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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

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