LifeTech Scientific Corporation Announces 2026 Interim Results
- The Group achieved revenue of approximately
RMB600.8 million during the Reporting Period.
- Gross profit was approximately
RMB465.9 million , while gross profit margin increased 3.9 percentage points to approximately 77.5% for the six months ended30 June 2026 . Excluding certain non-recurring items[1], net profit attributable to owners of the Company was approximatelyRMB114.8 million , during the Reporting Period.
- As at
30 June 2026 , the Group's cash and cash equivalents amounted to approximatelyRMB953.8 million , representing an increase of approximately 32.6% compared with31 December 2025 .
Note [1]: Such non-recurring items include (i) the other losses arising from financial assets at fair value through profit or loss; (ii) the share-based payment expenses; and (iii) the transaction expenses in connection with a proposed transaction involving the conditional acquisition of equity interest in Starway Medical Technology, Inc. and the issue of convertible bonds, which the Board has resolved not to proceed with. |
Tackling Domestic-market Challenges, Fueling Overseas Revenue Growth
In the first half of 2026, the Group maintained a sharp focus on addressing unmet clinical needs worldwide, leveraging its synergies in branding, intellectual property, distribution networks, clinical registration, and global operations. With an increasingly diversified and refined innovative product portfolio, complemented by professional academic services, the Group steadily consolidated its foundation for long-term growth.
Meanwhile, our overseas business maintained its upward momentum. The overseas sales of the Group grew by approximately 4.1% (approximately 8.2% in USD) year-on-year.
Long-term Focus,
Structural Heart Diseases Business
The Group has established a diversified product portfolio in the Structural Heart Diseases (SHD) business, mainly including LAA occluders and three generations of congenital heart diseases occluders, aiming to address various market demands through differentiated product strategies.
During the Reporting Period, the sales contributed by the SHD business were approximately
Continuous technological innovation and product upgrades will further enrich the SHD product portfolio of the Group and enhance its global sales layout.
Peripheral Vascular Diseases Business
The Group is committed to providing patients worldwide with technology-leading systematic and comprehensive interventional medical devices solutions to treat Peripheral Vascular Diseases (PVD).
The products offered by the Group in the PVD business mainly include vena cava filters, thoracic aortic aneurysm stent grafts, abdominal aortic aneurysm stent grafts, iliac artery bifurcation stent grafts, aortic stent graft systems, aortic arch stent graft systems and thoracoabdominal aortic stent graft systems.
During the Reporting Period, the sales contributed by the PVD business were approximately
Cardiac Pacing and Electrophysiology Business
The Group recorded no sales contribution from its cardiac pacing and electrophysiology business during the Reporting Period.
R&D and Commercialization Progress
The Group adheres to independent innovation, aiming to provide medical devices that deliver outstanding clinical value for physicians and patients worldwide, while continuously enhancing its long-term competitiveness.
During the Reporting Period, the Group invested approximately
During the six months ended
- Iliac Bifurcation Device (consisting of the G-iliac™ Pro Iliac Bifurcation Stent Graft System and SilverFlow™ Pro Internal Iliac Stent Graft System) and Peripheral High Pressure Balloon Dilatation Catheter have obtained the National Medical Products Administration ("NMPA") certification;
- G-iliac™ Iliac Bifurcation Stent Graft System and SilverFlow™ Internal Iliac Stent Graft System have obtained the CE MDR (Medical Device Regulation) certification;
- Cera™ PFO Occluder, CeraFlex™ PFO Occluder, FuStar™ Steerable Introducer, SeQure™ Snare System and SteerEase™ Introducer have obtained the CE MDR certification. Such products have previously obtained the CE MDD (Medical Device Directive) certification;
- Cera™ PFO Occluder, Yuranos™ Pro Abdominal Aortic Stent Graft System and Constraining Structure PTA Balloon Catheter, etc. are pending registration approval in
China ;
- Aortic Stent Graft System (consisting of the Ankura™ Pro Aortic Stent Graft System and Longuette™ Aortic Branch Stent Graft System), Fitaya™ Vena Cava Filter System, Futhrough™ Stent Graft Balloon Catheter, Yuranos™ Abdominal Aortic Stent Graft System, Thoracoabdominal Artery Stent Graft System (consisting of the G-Branch™ Thoracoabdominal Aortic Stent Graft System, SilverFlow™ PV Peripheral Vascular Stent Graft System, G-Branch™ AE Main Body Extension Stent Graft System, G-Branch™ AAA Bifurcated Stent Graft System and G-Branch™ IE Iliac Extension Stent Graft System) and Aortic Arch Stent Graft System (consisting of the Ankura™ Plus Aortic Arch Stent Graft System and CSkirt™ Aortic Arch Branch Stent Graft System) are pending registration approval of CE certification;
- X-Clip™ Mitral Valve Clip System and Nitinol Patent Ductus Arteriosus Occluder are currently at the stage of pre-registration clinical enrollment in
China ;
- CS™ Concave Supra-arch Branched Stent-Graft System and SureCham™ Aortic Arch Single Branch Stent Graft System (consisting of the Aortic Arch Stent Graft System and Aortic Branch Stent Graft System) have completed pre-marketing clinical enrollment and are currently under clinical follow-up in
China ;
- IBS Titan™ Sirolimus-Eluting Iron Bioresorbable Peripheral Scaffold System is currently at the stage of clinical enrollment in
China and inEurope , and its CE registration application has been submitted;
- IBS™ Sirolimus-Eluting Iron Bioresorbable Coronary Scaffold System has successfully completed the five-year follow-up of the phase I clinical study and the three-year follow-up of the phase II and III clinical study, further confirming its safety and efficacy. Additionally, its CE and NMPA registration application have been submitted; and
- CS™ Concave Supra-arch Branched Stent-Graft System has been admitted into the NMPA Special Examination and Approval Procedure for Innovative Medical Devices, which is the 17th product of the Company to have obtained admission to the Procedure.
Intellectual Property Rights
Intellectual property is an important intangible asset of the Group and also an internal driving force to improve our core competitiveness in the medical device market. As at
The Chairman and CEO of LifeTech, Mr. XIE Yuehui Said:
In the first half of 2026, the global medical device industry continued to undergo profound transformation. Despite external volatility posing certain challenges to the Group's short-term operations, we remained steadfast in our strategic focus, deepened our presence in core markets, and drove differentiated competition through technological innovation. Our product sales mix continued to improve, and all operational activities proceeded in an orderly manner.
Guided by our two core development strategies of "innovation" and "internationalization", we will accelerate breakthroughs in key technologies through forward-looking initiatives, further refine our systematic disease solutions, and leverage a more complete, diverse, and efficient portfolio of innovative products to steadily expand our global footprint and consolidate our industry‑leading position, thereby maintaining robust resilience amid the ongoing transformation and evolution of the global medical device sector.
The global healthcare industry holds vast prospects. Looking ahead, we will continue to focus on technological advancement and operational efficiency optimization. Leveraging our strong R&D capabilities, robust industrialization capacity, and outstanding global operation and management expertise, we aim to seize opportunities and address challenges to pursue sustainable and high‑quality growth, creating long‑term value for patients, healthcare institutions, shareholders, and all other stakeholders with unwavering dedication.
About LifeTech Scientific Corporation
Established in 1999 in Shenzhen, China, LifeTech Scientific Corporation (Stock Code: 1302.HK) specializes in the R&D, manufacturing, and sales of minimally invasive interventional medical devices for the treatment of cardio-cerebrovascular and peripheral vascular diseases. The Company offers innovative solutions for structural heart diseases, peripheral vascular diseases, bradycardia, and neurovascular conditions. It also possesses the world's first innovative iron-based bioabsorbable material technology platform. Guided by the core strategy of "innovation" and "internationalization", LifeTech maintains a leading market position for its key products in the home country and has established 7 subsidiaries overseas, extending its sales network to nearly 120 countries and regions worldwide.
View original content:https://www.prnewswire.com/news-releases/lifetech-scientific-corporation-announces-2026-interim-results-302862975.html
SOURCE LifeTech Scientific Corporation
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