# LifeTech Scientific Corporation Announces 2026 Interim Results

- Link: https://www.thailand-business-news.com/pr-news/lifetech-scientific-corporation-announces-2026-interim-results
- Published: 2026-08-28T23:23:00+07:00
- Author: PR Newswire

HONG KONG, Aug. 29, 2026 /PRNewswire/ — LifeTech Scientific Corporation ("LifeTech"
or the "Company", together with its subsidiaries, the "Group", stock code: 1302.
HK), a medical device company specializing in minimally invasive interventional 
solutions for cardio-cerebrovascular and peripheral vascular diseases, today announced
its unaudited consolidated results for the six months ended 30 June 2026 (the "Reporting
Period").

 ◦ 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 ended 30 June
   2026. Excluding certain non-recurring items^([1]), net profit attributable to
   owners of the Company was approximately RMB114.8 million, during the Reporting
   Period.

 ◦ As at 30 June 2026, the Group’s cash and cash equivalents amounted to approximately
   RMB953.8 million, representing an increase of approximately 32.6% compared with
   31 December 2025.

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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.

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**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.

China’s mainland remained the largest market of the Group, where the revenue generated
accounted for approximately 69.6% of the total revenue during the Reporting Period.

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.
Asia (excluding China’s mainland) and Europe were the two largest overseas markets
of the Group, which accounted for approximately 10.3% and 12.6%, respectively, of
the total revenue of the Group for the six months ended 30 June 2026.

**Long-term Focus, Deep Roots in Core Markets**

**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
RMB200.1 million.

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
RMB400.7 million, representing a year-on-year growth of approximately 2.3%, of which
the revenue generated from the sales of stent grafts and vena cava filters increased
by approximately 2.9% and 2.6% year-on-year, respectively.

**Cardiac Pacing and Electrophysiology BusinessThe 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 RMB167.1 million in
research and development (including capitalized expenditure). This investment will
further enhance our innovation capabilities, accelerate the development and commercialization
of our products, as well as to sustain our industry‑leading position.

During the six months ended 30 June 2026, we have achieved the following milestones
in the R&D field:

 ◦ 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 in Europe, 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 30 June 2026, the Group has filed a total of 2,608 valid patent applications,
of which 1,370 patents were registered and valid.

**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.

 

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