MedTech Business Review: Specials Magazine

A transcatheter route may be shared across procedures, but the anatomy is different in each valve position. Aortic stenosis, pulmonary regurgitation, mitral regurgitation and tricuspid regurgitation each place different demands on a replacement valve. Frame geometry, anchoring, sealing, coronary access and deployment behavior must also account for the anatomy. Venus Medtech [HKG: 2500] has built its structural-heart portfolio around those differences. Founded in 2009, the company develops transcatheter solutions across all four heart valves. It began with transcatheter aortic valve replacement (TAVR) and has since expanded into transcatheter pulmonary valve replacement (TPVR), as well as investigational transcatheter replacement programs for the mitral and tricuspid valves. The common thread is not one valve design repeated across indications. It is an approach that starts with the anatomical and procedural demands of each valve, then applies a different device design to address them. Control at the Aortic Valve VenusA-Valve established the TAVR pattern in the aortic space. Approved in China in 2017, it became the country’s first approved TAVR system. Its self-expanding frame was designed with enhanced radial force, which was intended to address the high incidence of bicuspid anatomy and heavy calcification among Chinese patients.

Technology alone does not change dentistry. Knowing how to use it does. At MV Dental Laboratory, every new digital tool, software platform and workflow is evaluated with one question in mind: will it help clinicians work more efficiently and deliver a better outcome for patients? That mindset has shaped a laboratory that is constantly testing, refining and adopting new ways of working rather than settling for yesterday's best practice. As a specialist Crown and Bridge laboratory with particular expertise in All-on-X, implant crowns and implant bridges, MV Dental Laboratory has built its reputation by combining advanced digital workflows with deep technical knowledge and close collaboration with clinicians across Australia. The result is a restorative process that saves valuable clinical time, reduces chairside adjustments and delivers predictable, natural-looking outcomes for patients. While many laboratories focus on investing in new equipment, owner Marc Meura believes the real competitive advantage lies elsewhere..

Medical Device Contract Manufacturer

CCB Medical Devices offers turnkey manufacturing solutions that empower medical innovators to navigate the complexities of global MedTech regulations, accelerating time to market by leveraging its integrated expertise in medical engineering and technical processing. Whether supporting startups with hands-on guidance or global healthcare brands with scalable and compliant solutions, CCB delivers tailored pathways to market success. Backed by two decades of technical expertise in manufacturing, CCB is actively expanding its robust capabilities beyond single-use airway management devices to include critical components for endoscopy, urology, and anesthesia. At the core of CCB’s mission is a steadfast commitment to high-stakes, high-precision manufacturing - where every detail carries the profound weight of human life and survival. To uphold this standard, its vertically integrated ecosystem spans the end-to-end supply chain, enabling seamless resolution of complex development challenges and ensuring the delivery of unwavering quality consistency. A key differentiator for CCB resides in its co-development model - a collaborative approach that transcends traditional contract manufacturing. Rooted in technology integrated with precision tooling development and flexible manufacturing automation, its facilities are highly adaptable, seamlessly supporting both high-mix, low-volume and high-volume production runs. “We view every customer as a partner and tailor our solutions to match the unique requirements and the complexity of each client’s needs,” says Dr. JS Khaw, Director. From early-stage prototyping and in-house tooling maintenance to full-scale cleanroom production, all stages are executed under one roof. This consolidated workflow minimizes vendor handoffs, enhances process control, and ensures complete traceability across development and production, speeding time to market while guaranteeing full regulatory compliance.

IN MY OPINION

Medical Suppliers and Distributors

From Activity to Impact: The New Standard in Healthcare Marketing

Mario R. Nacinovich Jr., MSc, Director of Marketing, Americas, BVI Medical and Host of The Spotlight Series Podcast, International Healthcare Media

LAST WORD

Medical Devices and Equipment Manufacturing

Medical Affairs in MedTech Is Increasingly Strategic: Here's Why

John B. Pracyk, MD, PhD, MBA, Chief Medical Safety Officer, Senior Vice President, Medical & Scientific Affairs, at Olympus Corporation

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EDITORIAL

Designing MedTech Around Clinical Needs

As medicine moves toward more personalized approaches, medical technology companies are rethinking how devices are designed and used. A valve cannot be built around a single anatomical model, and dental restoration workflows require tools that improve precision, planning and collaboration. This edition of MedTech Business Review APAC explores the companies and leaders developing solutions around these practical demands.

Our cover story features Venus Medtech [HKG: 2500], recognized as the Top Transcatheter Therapy Product in APAC 2026. Its structural heart portfolio spans all four heart valves, with different device designs developed around the anatomical and procedural demands of each. From the VenusA-Valve and VenusP-Valve to newer TAVR platforms and investigational mitral and tricuspid systems, the company has focused on deployment control, anchoring, sealing and future access rather than applying one design across every procedure.

Also recognized is MV Dental Laboratory, recognized as the Precision Dental Restorations Products Company of the Year in APAC 2026. Its digital workflows bring planning, design and manufacturing closer together for complex implant restorations, including All-on-X cases. The laboratory evaluates technology based on whether it improves clinical outcomes or efficiency, while its collaboration with dentists helps refine workflows around individual treatment needs.

The issue also features perspectives from leaders working across medical technology and clinical practice. Ana Bentancor, Dental Laboratory Technician at ClearChoice Dental Implant Centers, explores how digital imaging, CAD/CAM, photogrammetry and 3D printing are changing dental workflows and improving precision. Pasha Javadi, Global Head of Medical Affairs and Human Factors at Embecta, examines how medical affairs brings clinical evidence, patient and healthcare professional perspectives into product development, usability and lifecycle decisions.

Together, these stories show how the best medical technologies are shaped by a clear understanding of clinical challenges. We invite our readers to explore these perspectives and discover how engineering, digital capabilities and clinical expertise are influencing the future of medical technology across APAC.