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2025.02High-frequency surgical equipment was approved for Class III medical device registration certificate2025
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2025.02Ophthalmic phacoemulsification surgical equipment was certified by ANVISA (Agência Nacional de Vigilância Sanitária)2025
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2025.01Disposable multiple clip applier and ligating clip were officially approved for Class III medical device registration certificate2025
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2025.01Disposable powered circular stapler was approved for Class II medical device registration certificate2025
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2025.01EndoSure disposable powered endoscopic liner cutter stapler and cartridge were officially approved for Class III medical device registration certificate2025
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2024.10High-frequency surgical equipment was certified by ANVISA (Agência Nacional de Vigilância Sanitária)2024
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2024.10Ultrasonic high-frequency integrated surgical equipment and 7mm ultrasonic scalpel were officially approved for Class III medical device registration certificate2024
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2024.09Ultrasonic scalpel (including 7 mm tip) and phacoemulsification surgical equipment had obtained MDR (EU Medical Device Regulation) CE mark respectively2024
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2024.08EndoSure disposable powered endoscopic liner cutter stapler and cartridge were officially approved for medical device registration by the Provincial Medical Products Administration2024
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2023.10Innolcon's handpiece-integrated scalpel was officially approved for medical device registration certificate by the National Medical Products Administration2023
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2023.08Ophthalmic phacoemulsification surgical equipment was officially approved for medical device registration certificate by the National Medical Products Administration2023
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2023.05The new site of Lianchuang Industrial Park was officially put into operation2023
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2022.06The Advanced Bi-polar Surgical Instruments and the second generation of Ultrasonic Surgical System formed prototype2022
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2021.12Innolcon Hefei manufacturing base was founded2021
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2021.04Innolcon Phaco-emulsification Surgical System is the first Chinese brand that obtained CE Certification2021
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2021.04The Ultrasonic Surgical System obtained ANVISA Certification（Brazilian Health Regulation Agency）2021
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2021.01The Ultrasonic Surgical System obtained KFDA Certification（Korea Food and Drug Administration）2021
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2020.08The Ultrasonic Surgical System obtained the 5mm vessel sealing and cutting NMPA Certification2020
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2019.08The Ultrasonic Surgical System obtained CE Certification2019
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2018.09The manufacturing base in BioBay Phrase II was completed2018
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2017.07The Ultrasonic surgical instrument successfully passed the type inspection2017
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2016.12The first ultrasonic scalpel passed registration testing.2016
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2014.06The company was founded2014
