Medical technology innovators are pioneering new devices and technologies for one reason alone—to improve and save the lives of patients. To that end, patient safety is at the heart of what we do. The medical technology industry is committed to safety, effectiveness and quality for all devices. Medical technologies are thoroughly and rigorously tested by companies before they are submitted to FDA for exhaustive, science-based reviews.
Patient safety has always been and always will be our #1 priority. Over 49 million people live with implantable devices such as intraocular lens implants (IOLs), implantable cardioverter defibrillators (ICDs), pacemakers and artificial knees and hips. Patients turn to medtech to give them independence and opportunities, whether that means the ability to play with grandchildren or to return to work quickly. The medical technology industry puts patients’ needs first and creates innovative devices to improve lives around the world.
Throughout the lifecycle of a medical device, it is carefully tested, reviewed and modified to minimize risk. Rigorous testing, extensive FDA reviews and post-market reporting ensure medical devices are safe and effective for millions of patients.
Scientists. Physicians. Engineers. Quality Experts. Countless professionals thoroughly research and examine every aspect of a medical device. Every year the FDA subjects thousands of medical devices to intensive, scientific reviews based on extensive data to ensure that they meet their pre-determined specifications of safety and effectiveness. Industry and regulatory bodies work together to identify problems, create solutions and drive shared progress toward the shared goal of getting patients safe, effective products when they need them.
Thanks to lifesaving medical technology patients are living longer, happier, healthier and more productive lives. Five years added to U.S. life expectancy means more time with family, more birthdays and more life moments.