The creation of medical devices in the biomedical and implant industry presents a challenging and complex environment for attorneys and physicians who must deal with medical product liability issues. Such medical devices and implants can effect patient’s health in a number of different ways and the FDA has developed three levels of classification for regulatory purposes-Class I, Class II and Class III. These are what amounts to a quality control program to guarantee that new devices have undergone extensive testing and trials to establish their effectiveness and safety before being released into the marketplace. This development process for medical products can indeed be a complicated one especially for products classified under Class II or III.