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In the highly regulated and complex field of medical device manufacturing, having a partner who can provide comprehensive, end-to-end solutions is invaluable. At Cadence, we offer a complete suite of services that span the entire lifecycle of a medical device, from initial design and development to final assembly and after-market support. Our seamless integration of each phase ensures that we deliver high-quality, reliable products that meet the rigorous standards of the medical industry. Product Design and Development The journey of a medical device begins with a concept. At Cadence, our experienced teams work closely with clients to bring their ideas to life. We utilize advanced computer-aided design (CAD) software and simulation tools to create detailed models and prototypes. Our collaborative approach ensures that all aspects of the device, from functionality to manufacturability, are thoroughly considered. During the design phase, we focus on innovation and precision. Our engineers leverage their extensive knowledge of materials and processes to optimize the design for performance and cost-effectiveness. We also conduct rigorous testing and validation to ensure that the...

The medical device manufacturing industry continues to undergo a significant transformation, driven by advancements in technology, changing regulatory landscapes, and evolving patient needs. As we move forward, the focus is increasingly on precision, customization, and efficiency. Companies like Cadence, a leading Medical Device Contract Manufacturing Organization (CMO), are at the forefront of this change, leveraging their vertically integrated capabilities to provide complex, end-to-end manufacturing solutions. Trends Shaping the Future of Medical Device Manufacturing 1. Technological AdvancementsThe integration of advanced technologies such as artificial intelligence (AI), machine learning (ML), and the Internet of Things (IoT) is revolutionizing medical device manufacturing. These technologies enable better predictive maintenance, quality control, and supply chain management, ensuring higher precision and reliability in the production process. 2. Regulatory ChangesThe regulatory landscape for medical devices is becoming more stringent, with increased emphasis on patient safety and product efficacy. This requires manufacturers to adopt more rigorous testing and validation...

At Cadence, our work in medical device manufacturing goes beyond precision engineering and innovative solutions; it touches lives in the most profound ways. While we often focus on the global impact of our devices, today, we want to share a personal story from our own employees. We celebrate the incredible contributions of our team members who embody our commitment to innovation and excellence. Today, we honor Susie Weber, whose dedication and hard work have left an enduring legacy at Cadence and within the medical device industry.   A Life of Purpose Susie joined Cadence with a heart full of dedication and a work ethic that inspired everyone around her. Working in our secondary operations department, she took on some of the most challenging and physical tasks in our facility, demonstrating a relentless commitment to her work and to the people who would ultimately benefit from it. Despite the demanding nature of her job, Susie's spirit and determination never wavered.   Impact Through Innovation One of Susie's most significant contributions was her work on a crucial project – a staple remover and suture remover. These devices, which are essential for post-surgical care,...