Home Medical Device Weekly Highlights (May 25–31, 2026): Funding, Approvals, M&A, and Global Expansions

Medical Device Weekly Highlights (May 25–31, 2026): Funding, Approvals, M&A, and Global Expansions

Jun 02, 2026 08:00 CST Updated 08:00
Neuraic

Invasive Brain-Computer Interface Developer

ROBO Medical

Medical Robot Developer

LifeTech

Suppliers of Congenital Heart Defect Occluders

Starway Medical

Research and Development, Production of Cardiovascular Interventional Devices

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01


Neuraic Completes Angel Round Financing

Recently, Neuraic, a hard-tech startup focused on the clinical translation of brain-computer interfaces (BCI) and led by Dr. Gu Huidong, completed a tens-of-millions-yuan angel financing round. The round was led by Enran Venture Capital, with participation from Hangzhou Runmiao Fund and West Lake Photonics, and co-investment from Shanghai Angel Club. Behind this rush of capital lies a formidable technological moat. Neuraic has industrialized twenty years of technical accumulation from the Institute of Semiconductors, Chinese Academy of Sciences, overcoming two major hurdles in the field of invasive BCIs: excessive trauma from flexible electrode implantation and rapid signal decay within a short period. Its self-developed semiconductor hollow flexible electrodes, combined with a proprietary "physiological saline rigid adjustment" process and a 13-micron-level minimally invasive implantation pathway, have achieved dual breakthroughs in animal models: a 70% reduction in acute injury and stable neural signals sustained for six months.

02


ROBO Medical Completes Tens of Millions in FundingSeries B+ Financing

ROBO Medical, the company behind the approved digestive endoscopic surgical robot, has officially announced the successful completion of a financing round amounting to tens of millions of RMB. The round was led by Shuimu Ventures, with strategic investor Boyue Tiancheng participating, and Siche Consulting serving as the exclusive long-term financial advisor. The funds raised will be primarily allocated to the nationwide clinical deployment of its core product, the EndoFaster® (Su Yi Bi) digestive endoscopic surgical robot; the research and development of its next-generation product, EndoDreams; the construction of an intelligent manufacturing base and supply chain optimization; as well as international market certification and hospital adoption promotion.

03


Lifetech Scientific withAcquisition of Starway Medical for RMB 1.87 Billion

Lifetech Scientific Acquires Approximately 96.46% Equity Stake in Starway Medical for RMB 1.87 BillionLifetech Scientific, a company specializing in the research and development of interventional devices for cardiovascular, cerebrovascular, and peripheral vascular applications, has acquired approximately 96.46% of the equity interest in Starway Medical for RMB 1.87 billion. Lifetech Scientific reported revenue of RMB 1.37 billion in 2025. While its structural heart disease business experienced a decline, its peripheral vascular business became a key growth driver, although its vena cava filters were included in the volume-based procurement program.Starway Medical focuses on vascular interventional devices and possesses four core occluder products, with over 220,000 cumulative clinical implantations. The acquisition of Starway Medical will fill Lifetech Scientific’s gap in patent foramen ovale (PFO) occluders. Given the substantial potential market size for PFO occluders in China, this acquisition will provide Lifetech Scientific with mature products and strengthen its structural heart disease product portfolio.Starway Medical is effectively controlled by Hillhouse Capital. This transaction does not involve cash payments. Following the merger, Lifetech Scientific will integrate resources and optimize its strategic layout, which is expected to unlock new growth opportunities.

04


Shenzhen Ruixin Intelligent Medical Technology Co., Ltd. Completes Nearly 100 Million Yuan in FinancingSeries D Financing

Recently, Shenzhen Ruixin Intelligent Medical Technology Co., Ltd. completed a Series D financing round of nearly RMB 100 million, led by Guangzhou Health Industry Investment and followed by Yuefu Fund, with its operations established in Yuexiu District, Guangzhou. This financing round demonstrates recognition of Ruixin Medical’s core technologies, industrial value, and commercialization progress, and will inject momentum into the company’s overall pipeline development, business growth, and expansion into overseas markets. Following this financing, Ruixin Medical will deepen its layout of AI-driven vascular interventional surgical robot systems and build an integrated AI + robotics diagnosis and treatment platform. The company focuses on precise cardiovascular diagnosis and treatment and has built an integrated intelligent diagnostic and therapeutic platform. Its core product, AngioQFA, has become a benchmark for precise coronary artery diagnosis and treatment; Ruixin Fraction (CT-FFR) is continuously advancing clinical implementation; and its new deployment of intracardiac echocardiography (ICE) further completes the diagnostic and therapeutic closed loop. In the future, Ruixin Medical will continue to deeply cultivate the field of precise cardiovascular diagnosis and treatment.

05


Medprin Medical plans toAcquisition of Yijie Medical for RMB 335 Million

On May 25, Medprin Regenerative Medical Technologies Co., Ltd. (“Medprin”), a leading domestic neurosurgical company, proposed to acquire 100% equity interest in Yijie Medical, a neurointerventional company, for RMB 335 million, thereby entering the high-growth neurointerventional sector. Established in 2020, Yijie Medical has a comprehensive pipeline of products under development and has built four major technology platforms. Medprin has long been deeply engaged in the neurosurgical field with stable performance growth; however, the growth potential of the neurosurgical medical device market is limited, and normalized volume-based procurement has narrowed profit margins. This acquisition will help Medprin expand its business into the neurointerventional field, strengthen strategic synergies, and integrate channel resources to broaden sales coverage. Medplin plans to leverage its biodegradable biomaterials technology platform, combined with trends in neurosurgical treatment, to develop therapeutic products for interventional procedures, with multiple projects currently planned for research and development. Furthermore, since the beginning of this year, mergers and acquisitions in China’s medical device market have continued unabated. For leading enterprises, entering new sectors or strengthening existing businesses through M&A has become an important strategic initiative.


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06


AI-Native Electronic Health Record System Receives EU Medical Device Certification

Recently, InterSystems announced that its IntelliCare electronic health record (EHR) solution has obtained Class IIa medical device certification under the European Union’s Medical Device Regulation (MDR), specifically Regulation (EU) 2017/745. IntelliCare is positioned as the first native AI-powered EHR system to achieve MDR Class IIa certification. Built on the interoperability foundation of InterSystems TrakCare, IntelliCare is designed as a next-generation EHR system with integrated artificial intelligence capabilities. Unlike systems that rely on third-party AI plug-ins, IntelliCare embeds AI directly into the platform’s data layer, enabling seamless integration of intelligent features throughout clinical workflows.

07


DesaiAI Medical Imaging Products Approved for Class III Medical Device Certification

Recently, Hangzhou DeShi Biotechnology Co., Ltd. announced that its independently developed AI AutoVision software for assisted diagnosis of chromosome karyotyping has officially received the Class III Medical Device Registration Certificate issued by the National Medical Products Administration (NMPA). By analyzing images of chromosomes in metaphase, and combining traditional image processing techniques with artificial intelligence algorithms, the product can automatically perform chromosome cutting, counting, identification, arrangement, and provide assisted alerts for abnormalities, thereby improving detection efficiency and offering more efficient assisted diagnostic services to patients. The product is powered by DeShi’s self-developed iMedImage, a foundational large model for medical imaging. Previously, traditional large models for medical imaging were often limited to single diseases, involving high development costs and lengthy approval cycles. In contrast, the iMedImage foundational large model possesses generalizable capabilities across imaging data for multiple disease types, requiring only approximately 200 cases and a training period of two to three months to adapt to various diseases.

08


Sentire® Endoscopic Surgical Robot Receives Dual Certification from EU CE and Singapore HSA

May 25, 2026 – Coronostem’s independently developed Sentire® laparoscopic surgical robot has received dual certification from the European CE and Singapore’s Health Sciences Authority (HSA), making it suitable for endoscopic surgeries across multiple specialties. This breakthrough marks its official approval to enter the core healthcare markets of Europe and the Asia-Pacific region. Previously, the robot completed clinical trials in the UK, validating its clinical application capabilities. By deeply integrating multiple technologies, the Sentire® system’s CE certification demonstrates that its safety, efficacy, and quality management systems fully comply with stringent international regulatory standards, equipping it with the strength and qualifications to serve patients and healthcare providers worldwide. The company had earlier established a branch in the UK, leveraging its global R&D center to absorb resources, and partnered with British hospitals to launch clinical evaluation projects, accumulating real-world data. Furthermore, Coronostem has established a strategy of “being rooted in China while keeping a global perspective,” building a full-lifecycle, one-stop localized service system in Europe.

09


Ruichu Robotics Plans to List in Hong Kong

On May 22, 2026, Shanghai Ruichu Robotics received the filing notice for overseas listing from the China Securities Regulatory Commission (CSRC), indicating its intention to list in Hong Kong within 12 months. Founded in 2019, the company focuses on CT-guided percutaneous puncture robots, with a team largely drawn from medical imaging enterprises and a technical approach centered on the integration of “medical imaging + robotics.” Currently, R&D personnel account for approximately 50% of the workforce. The company has filed over 80 patents across multiple areas, with its flagship product being the RC120 lung puncture robot, which obtained Class III medical device registration certification from the National Medical Products Administration (NMPA) in February 2024. Lung puncture procedures have long relied on physicians’ experience, often requiring repeated adjustments to the puncture path in complex cases. While current market solutions commonly depend on optical or electromagnetic navigation systems, the RC120 attempts to achieve coordinate localization and path guidance directly based on CT images, thereby reducing the need for external sensor deployment and manual registration processes.


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10


Unveiling of the Global Medical Device Training, Exhibition, Trading, and Innovation Center in the Shanghai Eastern Hub International Business Cooperation Zone

Recently, the unveiling ceremony of the Global Medical Device Training, Exhibition, Trading and Innovation Center and the operational launch of its first batch of projects, themed “Gathering Global Momentum, Innovating for the Future of Healthcare,” was officially held. The event was guided by the Administration Bureau of the Shanghai Oriental Hub International Business Cooperation Zone, jointly hosted by Waigaoqiao Group and Boston Scientific, and co-organized by Danaher and Siemens Healthineers. At the event, the Global Medical Device Training, Exhibition, Trading and Innovation Center was officially unveiled. As a key project of the center and Boston Scientific’s global open hub for medical technology innovation, the A3 International Medical Technology Innovation Exchange Center was simultaneously put into operation. This marks a critical step for the Shanghai Oriental Hub International Business Cooperation Zone in aggregating global healthcare innovation resources and promoting international collaborative innovation. It also signifies the exploration in Shanghai of a future-oriented model for collaborative medical innovation: accelerating the maturation of cutting-edge global innovations through rich and complex clinical practices, while leveraging frontline innovative experiences and clinical insights to provide new inspiration for global healthcare innovation.

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11


Gemdale Smart Services Ramps Up Investment in the Medical Device Sector

Recently, Gemdale Commercial Services, a subsidiary of Gemdale Smart Services, has fully entered Biomime Medical’s global headquarters to provide full-cycle integrated property and facility management services. This marks another significant strategic move by Gemdale Commercial Services in the intelligent manufacturing sector of medical devices, following its service engagement with Mindray Medical. It not only demonstrates the company’s comprehensive strength in serving national-level “Specialized, Refined, Differential, and Innovative” (SRDI) enterprises but also helps accumulate experience in providing full-cycle services for biomedical industrial parks. Having been rooted in Songshan Lake for 14 years, Biomime Medical has become a national high-tech enterprise, leading in vascular interventional device technology. The company has accumulated over 200 patents, with multiple technologies filling domestic gaps. Its global headquarters base, located in the core area of Songshan Lake, is a key construction project in Dongguan City. The relocation and occupancy were recently completed, with Gemdale Commercial Services’ team simultaneously commencing full-scale on-site operations.


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12


Liaoning Provincial Drug Administration Solicits Public Comments on the “Provisions for the Supervision and Administration of Automatic Vending Machines for Medical Devices in Liaoning Province (Trial) (Draft for Comment)”

Recently, the Liaoning Provincial Drug Administration publicly solicited opinions on the "Provisions on the Supervision and Administration of Medical Device Vending Machines in Liaoning Province (Trial) (Draft for Comments)," aiming to regulate the operation of medical device vending machines within the province, clarify their positioning as an extension of retail premises, implement corporate primary responsibilities, and prevent quality and safety risks. The draft applies to the sale of medical devices via vending machines and related regulatory activities throughout the province. It requires operating enterprises to possess corresponding qualifications (Class I devices and Class II devices exempt from filing do not require qualifications; Class II devices require filing, and Class III devices require licensing). Vending machines shall be subject to networked management with a unique identifier per machine, featuring unified filing, unified labeling, unified distribution, and unified after-sales service, and must be equipped with functions such as temperature and humidity monitoring, data upload, and issuance of sales receipts. The categories permitted for sale are limited to Class I devices, Class II devices exempt from filing, and certain commonly used Class II devices; the sale of Class III devices and high-risk products is prohibited. The draft specifies requirements for placement locations (specific areas such as medical institutions and elderly care facilities), quality management systems, regular inspection and maintenance, traceability and recall, and information disclosure. Furthermore, it details regulatory responsibilities, supervision and inspection, handling of violations, and legal liabilities.

13


European Medicines Agency Launches Pilot Project for Breakthrough Medical Devices

Recently, the European Medicines Agency (EMA) launched a two-year pilot project for breakthrough medical devices, implemented in three phases. The first phase, focusing on cardiovascular diseases, will run until the end of 2026. The second phase is scheduled to begin in the first quarter of 2027 and will be open to all therapeutic areas. The third phase, starting in the third quarter of 2027, will be accessible to in vitro diagnostic (IVD) manufacturers and notified bodies. The project aims to assist manufacturers of breakthrough medical devices in obtaining regulatory approval in the European Union, thereby supporting the faster market entry of novel diagnostic or therapeutic products. Coordinated by the EMA, the initiative provides free consultation through expert panels and national competent authorities of Member States, helping IVD manufacturers and notified bodies navigate the new approval pathway. Representatives of IVD manufacturers have expressed support for the initiative, noting that it will encourage more innovators to view Europe as a “launch region,” and that the inclusion of IVDs in the pilot represents a positive development.


Note: The information in this article is compiled and summarized from online news sources.



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