MicroPort Orthopedics Inc.
1998-05-15
China
Robotic surgical systems for orthopedics
Clinical education and training services
Customer support and clinical assistance
interventional treatment of coronary artery-related diseases
coronary stent systems
balloon catheters
OCT imaging catheters
research and development
production
marketing
services
Zhangjiang Science City, Shanghai, China
会社名
Group 親会社 子会社 得意先 仕入先 業務提携 銀行等 株主等

105 件
日付概要
1998年 MicroPort® was founded in 1998 in a small office in ZJ Hi-Tech Park in Shanghai, by a group of dedicated individuals who shared the belief that advancements in medical technology could transform patients’ lives.
1998-05-15 Founded on May 15, 1998 at an incubation center in Zhangjiang Hi-Tech Park, Shanghai.
1999年 PTCA balloon dilatation catheter received SFDA approval, very first sale made.
2000年 Mustang™ bare metal stent received SFDA approval.
2002年 Received major funding from National Development and Reform Commission.
2003年 Officially entered Japan market with PTCA Balloon dilatation catheters.
2004年 Firebird™ drug eluting stent system received SFDA approval.
2004年 Mustang™ coronary stent system received CE mark.
2005年 Aegis Bifurcated Stent-Graft System was named National key new product.
2005年 Annual sales exceeded 100 million RMB.
2006年 Hercule® Thoracic Stent-Graft System received SFDA approval.
2006年 Coronary drug eluting stent implants reached over 100,000 units.
2007年 Firebird™ coronary drug eluting stent system won State Science and Technology Advancement Award.
2008年 Shanghai MicroPort Lifesciences Co., Ltd. was established, officially entered diabetes business; diversified business strategy implemented.
2008年 Began experimental implementation of "Vertical Integration & Horizontal Connection" management model.
2009年 Firebird2™ coronary drug-eluting stent system received registration approval from SFDA.
2009年 Shanghai MicroPort Orthopedics Co., Ltd. was established.
2010年 MicroPort Scientific Corporation listed on Hong Kong Stock Exchange (00853.HK).
2010年 Annual sales exceeded 100 million USD.
2010年 Shanghai MicroPort EP MedTech Co., Ltd. was established.
2011年 MicroPort Medical (Jiaxing) Co., Ltd. was established.
2011年 Undertook national R&D projects accumulating to more than 100 million RMB.
2011年 Shanghai MicroPort Orthopedics Co., Ltd. acquired Suzhou Best Co., Ltd.
2012年 Initiated “10+5” Operating Model.
2012年 Shanghai MicroPort® NeuroTech Co., Ltd., Shanghai MicroPort Endovascular MedTech Co., Ltd. and MicroPort Surgical (Shanghai) Co., Ltd. were established.
2012年 Acquired D-Pulse Medical (Beijing) Co., Ltd. and Dongguan Kewei Medical Instrument Co., Ltd.
2013年 MicroPort® Orthopedics Global Headquarter was established in Arlington, TX, USA.
2013年 Globalization Strategy Implemented.
2014年 Firehawk® rapamycin target eluting coronary stent system received CFDA approval.
2014年 WILLIS® clinical application project won State Science and Technology Advancement Award.
2014年 Signed joint venture agreement with Sorin Group for China's cardiac rhythm management business.
2014年 Acquired drug eluting stent related assets and intellectual properties from Cordis.
2014年 Moved into new headquarter on at 1601 Zhangdong Rd, Zhangjiang Hi-tech Park.
2014年 Annual sales exceeded 2 billion RMB.
2015年 MicroPort® Innovation Platform won State Science and Technology Advancement Award.
2015年 Firehawk® Rapamycin Target Eluting Coronary Stent received CE mark.
2015年 EVOLUTION® medial-pivot knee system received CFDA approval.
2015年 MicroPort Sorin CRM (Shanghai) Co., Ltd. launched China's first domestic pacemaker production line.
2015年 MicroPort Suzhou OrthoRecon Co., Ltd. and MicroPort Suzhou Orthopedic Instruments Co., Ltd. were established in Suzhou Industrial Zone.
2015年 MicroPort Surgical Robotics Co., Ltd. and MicroPort Online Co., Ltd. were established.
2015年 Founded in 2015, MicroPort
2016年 New Technology and Clinical Application of Minimally Invasive Cardiac Surgery project won the State Science and Technology Advancement Award.
2017年 Proposed to acquire the cardiac rhythm management business of LivaNova for $190 million in cash.
2017年 AAA/TAA stent graft series product critical technical development and large-scale industrialization won State Science and Technology Award.
2017年 Rega® Family Implantable Pacemakers and Firefighter™ PTCA Balloon Catheters received CFDA approval.
2017年 The data of Firehawk® TARGET AC clinical trial showed the 3-month stent strut cover rate was of 99.9%, 5-year follow-up data of TARGET I RCT showed stent thrombus rate was 0.
2017年 Medial-Pivot Knee arthroplasty system demonstrated high survivorship (98.8%) and patient satisfaction (95%) in a 17-year follow-up study.
2017年 Firesorb® pivotal study FUTURE II trial completed first enrollment.
2017年 MicroPort® CardioFlow brought in strategic investors.
2017年 MicroPort® EP quoted on NEEQ.
2017年 MicroPort Urocare Co., Ltd. established, marking the company's official entry in urology and gynecology sectors.
2017年 MicroPort® Jiaxing park established.
2017年 Acquired Brazil distributors to implement localized management on the Brazil market.
2018年 Firehawk® clinical data from the Target AC European clinical trial has been accepted for publication in the prestigious medical journal The Lancet.
2018年 Tubridge® Vascular Reconstruction Device was launched.
2018年 Firehawk® and Firebird2® gained regulatory approval in Taiwan.
2018年 First implantation of Rega® Family Implantable Pacemakers.
2018年 Global aggregated implantations of coronary artery stent system, artificial joint implants and pacemakers reached 4.5 million, 1.1 million and 1 million respectively.
2018年 MicroPort® CRM global headquarter was established in Clamart, France.
2018年 MicroPort Orthopedics (Suzhou) Co., Ltd. was established.
2018年 Every 12 seconds, a MicroPort® product was used across the world.
2019年 SoSuperior™ Medial Stability Total Knee Replacement System and Aspiration™ Medial Pivot Total Knee Replacement System gained approval in China.
2019年 MicroPort® Obtained CE Mark for Firehawk Liberty™, a New Generation Rapamycin Target Eluting Coronary Stent System.
2019年 The 24 months results of the Firehawk® TARGET AC trial were announced in EuroPCR 2019, and would be published in the Journal of the American College of Cardiology (JACC).
2019年 Every 6 seconds, a MicroPort® product was used across the world.
2020年 The MicroPort Group and its associated companies introduced external financing of over US$1 billion accumulatively and widely recognized by the capital market.
2021年 MicroPort® CardioFlow Medtech was listed on the Main Board of the Hong Kong Stock Exchange
2021年 MicroPort® MedBot® was listed on the Main Board of the Hong Kong Stock Exchange
2021年 MicroPort® CRM introduced the Alizea™ and Borea™ pacemakers equipped with Bluetooth technology and the SmartView Connect™ home monitor in Europe.
2021年 MicroPort® CRM Navigo™ left ventricular pacing leads received CE mark approval in Europe
2021年 MicroPort NeuroTech™ U-track Intracranial Support Catheter System became commercially available in the market
2021年 EverPace Disposable Cardiac Mapping Leads became commercially available in the market
2021年 Firefighter™ and Foxtrot® Pro PTCA Balloon Dilatation Catheter approved for marketing in Pakistan and Bosnia and Herzegovina
2021年 HorizonMedical™ Daylily® Embryo Transfer Catheter approved for marketing in Thailand
2021年 Four products including Firehawk® Stent and Firefighter™ PTCA Balloon Dilatation Catheter received registration and marketing approval in Saudi Arabia
2021年 Firefighter™ NC received registration approval in Taiwan.
2022年 MicroPort NeuroTech was listed on the Main Board of the Hong Kong Stock Exchange
2022年 MicroPort MedBot Skywalker™ Orthopedic Surgical Robot received NMPA approval in China, FDA 510(k) approval in the US and CE mark approval in Europe
2022年 MicroPort NeuroTech Diveer® Intracranial Balloon Catheter, Neurohawk® Stent Thrombectomy Device, X-track® Intracranial Distal Access Catheter, and NUMEN Silk® 3D Electronically Detachable Coil received NMPA approvals in China
2022年 MicroPort MedBot Toumai® Laparoscopic Surgical Robot received NMPA approval in China and won several awards
2022年 MicroPort® CRM Invicta™ Defibrillation leads received CE mark approval in Europe
2022年 MicroPort Endovascular Talos® Thoracic Stent Graft System received NMPA approval in China
2022年 MicroPort Urocare Single-use Flexible Digital Ureteroscope received the NMPA approval in China
2022年 MicroPort Argus™ intravascular OCT system received NMPA approval in China
2022年 MicroPort® inaugurated a training Center in Brazil
2024年 MicroPort® obtained 4 FDA approvals, including: MicroPort® Orthopedics EVOLUTION® Tibial Cones
2024年 58 products obtained NMPA's approval in China, including: MicroPort® Orthopedics Evolution® CCK Knee Revision System
2024年 And 6 products entered NMPA's "Green Path", including: MicroPort® Orthopedics Wrist Arthroplasty System
2025年 MicroPort® CardioFlow completed a strategic merger with MicroPort® CRM, building a comprehensive heart failure management solution spanning all etiologies, stages, and treatment pathways.
2025年 MicroPort® obtained 7 FDA approvals, including: MicroPort® Orthopedics NEXUS® Femoral Stem.
2025年 MicroPort® obtained 23 CE approvals, including: MicroPort® Endovastec™ Hector® Multi-Branch Thoracic Stent Graft System (custom certification).
2025年 MicroPort® obtained 23 CE approvals, including: MicroPort EverPace™ IceMagic™ Cryoablation System.
2025年 MicroPort® obtained 23 CE approvals, including: MicroPort® CRM MR-Conditional Mixed Pacing System and VEGA™ M lead.
2025年 Over 30 products received NMPA Class III medical device registration, including: MicroPort® Coronary TomaHawk® Intravascular Lithotripsy Catheter and Firelimus® Drug-Eluting Balloon, MicroPort® CardioFlow AnchorMan® Left Atrial Appendage Closure System, MicroPort® CRM TEN Series 3.0T MRI-Conditional Pacemakers, MicroPort® Endovastec™ Cratos™ Thoracic Branch Stent Graft, MicroPort EverPace™ PulseMagic™ TrueForce® PFA Catheter, MicroPort® MedBot UniPath® Surgical Navigation System and Toumai® SP Single-Port Robot, MicroPort® VisionPower YINI® Cataract Phacoemulsification System, MicroPort® MicroVasive EZ-Eye™ 5100 GI Endoscopy System, MicroPort® Dentition YairDent® Dental Implant System.
2025年 41 products were accepted into the NMPA’s 'Green Path', including: MicroPort® Endovastec™ Hector® Multi-Branch Thoracic Stent Graft, MicroPort® UniFlow Streamliner™ Implantable Tibial Nerve Stimulator, MicroPort EverPace™ EasyEcho™ Intracardiac Ultrasound Catheter, MicroPort NeuroScientific StraitPass™ Disposable Hematoma Aspiration Device.
2025年 MicroPort® CRM VEGA™ M58 Pacing Lead approved in Australia, MicroPort® CardioFlow VitaFlow Liberty® Transcatheter Aortic Valve System approved in 15 countries, including Brazil and Morocco, MicroPort® MedBot Toumai® Remote Surgery System approved in 10 countries.
2025年 TARGET-FIRST Trial results for MicroPort® Coronary Firehawk® Stent published in The New England Journal of Medicine and presented at ESC 2025, demonstrating safety of 1-month DAPT in low-risk AMI patients with complete revascularization.
2025年 MicroPort® Coronary surpassed 10 million stent systems shipped and implanted globally.
2025年 MicroPort® MedBot Toumai® Surgical Robot achieved over 100 global commercial installations.
2025年 The Toumai® system also achieved multiple robotic surgery milestones, including: The world’s first commercial remote robotic surgery.
2025年 The Toumai® system also achieved multiple robotic surgery milestones, including: The first FDA-IDE approved remote robotic surgery.
2025年 The Toumai® system also achieved multiple robotic surgery milestones, including: The first remote robotic surgery in Europe.
2025年 The Toumai® system also achieved multiple robotic surgery milestones, including: The first ultra-remote 5G robotic surgery at over 4,500 meters altitude.
2025年 The Toumai® system also achieved multiple robotic surgery milestones, including: The first low-orbit satellite remote surgery.
2025-06-11 MicroPort® CardioFlow’s VitaFlow Liberty® Expands Global Presence with Key Milestones in Europe and Latin America
+ 開くと読み込みます
2026-06-30 17:40 (Model: ggml-org/gpt-oss-20b )
↑