Device Events LLC is a Pennsylvania-based company that provides a cloud-based software service that extracts, consolidates and provides clear and comprehensive metrics and reports on the millions of complex medical device adverse event reports (MDRs) and recalls that have been filed with the FDA. Our service helps all organizations associated with healthcare by providing them with clear, comprehensive and cost effective access to the most up to date information on problem medical devices. We are committed to making information on problem devices easily accessible to our customers so they can improve health outcomes and patient safety while reducing risk for their organizations.
Facts & figures about dental implants – the second most reported medical device to the FDA.
Dr. Dirk Duddeck, CEO and Founder of the CleanImplant Foundation speaks with Madris Kinard-Tomes, FDA data analyst and CEO of Device Events (https://www.deviceevents.com). The interview sheds new light on implants of inferior quality. Factory-made contaminants have consequences, such as inflammatory processes, bone loss, and even implant failure. Uncontrolled foreign body reactions directly affect patients. Madris reports on breathtaking FDA data of adverse events related to dental implants. Click on the image or start the video here: https://youtu.be/sPMxcSc49pg