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CCB Medical Devices has been recognized by Medtech Business Review Magazine as the exclusive recipient of “Top Medical Device Contract Manufacturer in APAC - 2025,” based on our proprietary methodology, reflecting its position in the industry. This profile has been developed by the Medtech Business Review research and editorial team based on insights from an interview with Dr. JS Khaw, Director.
Dr. JS Khaw, DirectorCCB 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.
CCB’s comprehensive manufacturing expertise, paired with diverse capabilities spanning plastic and silicone extrusion or molding techniques, and assembly processes, forms the foundation of a full-cycle manufacturing model rooted in material intelligence. This model delivers strong right-first-time performance, greater predictability, and streamlined outcomes across every stage, with its influence taking hold as early as the concept phase. From this early phase, CCB helps clients avoid costly rework by optimizing material selection, product and component design, and toolmaking strategies, ensuring efficiency and reliability are built in from the very start.
With a deep understanding of the medical industry’s strict requirements, CCB places compliance at the forefront of its manufacturing process. It adheres strictly to the ISO 13485 Quality Management System, U.S. FDA regulations, and EU MDR standards, prioritizing quality and precision across every stage of the product lifecycle.
The company also strongly emphasizes on sustainability, talent development and future readiness. Its green and lean manufacturing initiatives reflect a commitment to environmental responsibility without compromising efficiency or quality. In parallel, ongoing investment in talent development ensures that its engineers, operators and quality specialists stay ahead of technological shifts and regulatory changes.
More than a contract manufacturer, CCB Medical Devices offers long-term support to help clients adapt, scale and succeed in one of the world’s most regulated industries.
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