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2026.04Integrated Ultrasonic and High Frequency Surgical Generator and Ultrasonic Surgical Scalpel (Built-in Hand Piece) were marked by EU MDR Certification2026
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2026.03-04High Frequency Equipment have been approved for market launch in Hong Kong (China), Malaysia, Kyrgyzstan, and Ukraine2026
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2026.03Ophthalmic Phacoemulsification Equipment have obtained market approved in India2026
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2026.02Ultrasonic Surgical Scalpel (Reusable) Obtained Class III Medical Device Registration Certificate in China2026
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2026.02Absorbable Surgical Sutures Obtained Class III Medical Device Registration Certificate in China2026
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2026.01Disposable Endoscopic Trocar Obtained Anhui Province Class II Medical Device Registration Certificate2026
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2025.12Ultrasonic Surgical Scalpel (7mm, Built-in Hand Piece) Obtained Class III Medical Device Registration Certificate in China2025
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2025.12Disposable Powered Articulating Endoscopic Linear Cutter Stapler and Reload Obtained Class III Medical Device Registration Certificate in China2025
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2025.11Disposable Polyurethane Closed Negative Pressure Drainage Set Obtained Anhui Province Class II Medical Device Registration Certificate2025
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2025.11Ultrasonic Surgical Scalpel (7mm) Obtained Class III Medical Device Registration Certificate in China2025
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2025.11Medical Vacuum Suction Device Obtained Anhui Province Class II Medical Device Registration Certificate2025
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2025.11Disposable Endoscopic Linear Cutter Stapler and Reload Obtained Anhui Province Class II Medical Device Registration Certificate2025
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2025.10High Frequency Equipment have obtained market approved in South Korea and Australia2025
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2025.10Disposable Neutral Electrode Obtained Jiangsu Province Class II Medical Device Registration Certificate2025
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2025.08IPO Launched2025
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2025.08High Frequency Equipment have obtained market approved in Saudi2025
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2025.08Type Testing of Thoracic and Laparoscopic Minimally Invasive Surgical Robotic System2025
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2025.07Ultrasonic Surgical Scalpel Obtained Class III Medical Device Registration Certificate in China2025
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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 Equipment marked by ANVISA (Brazil)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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2024.10Integrated Ultrasonic and High Frequency Surgical Generator and Ultrasonic Surgical Scalpel (7mm) were officially approved for Class III medical device registration certificate2024
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2024.09Ultrasonic Surgical Equipment (including Ultrasonic Surgical Scalpel) and Phacoemulsification Surgical Equipment were marked by EU MDR Certification2024
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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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2023.10Ultrasonic Surgical Scalpel (Built-in Handpiece) 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 Bipolar Surgical Equipment and the second generation of Ultrasonic Surgical Equipment (with RF energy) 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
