The Utah Supreme Court will decide whether to apply to medical devices a key legal doctrine that protects manufacturers of technologically-advanced products from the unfair application of strict liability.
News & Features
Bose Corp. has developed a hearing aid that FDA said is the first device that enables users to fit, program, and control without the assistance from a health care provider.
The agency is encouraging innovation in digital health. But is software really so fundamentally different from hardware that it can’t be regulated in the same way?
The Wayne, PA-based company is picking up Essential Medical to help bolster its presence in the structural heart market.
Industry and FDA are working together to promote actual quality improvement, not just compliance to regulations.
The MD&M Panel is titled Deep Brain Stimulation: How Will New Electrode Designs Improve Results and will be held Nov. 1.
Machines could learn like humans, offering quality and productivity benefits, among others, according to an automation and machine vision expert speaking at MD&M Minneapolis.
A Cleveland Clinic surgeon talks about the future potential of a new single-port robotic surgery system.
An industry expert said with the healthcare business model changing, providers need to implement the right tools for patient-centric care with access to the right information.
Designers should understand the commercial, technical, and compliance aspects of manufacturing to produce devices effectively while minimizing costs, says an expert speaking at MD&M Minneapolis’s MedTech Central.