Medtech design engineers these days are challenged to make medical and dental devices that are smaller and portable yet do much more than ever before—process data, connect to the cloud, and utilize AI ...

Engineers could avoid expensive redesigns by planning medical device testing early in development with expert guidance.

Small medtech companies can leverage AI without huge investments to compete with major manufacturers using targeted approaches.

Successful new medical devices hinge on the designer’s understanding of the specific requirements of the procedures they support, including factors like usage frequency and duration. This is ...

The pandemic has forced remote product development in many fields, and the medical device arena has seen rapid growth in the use of virtual reality (VR). Studying the potential outcomes for individual ...

The world is changing. Oil prices have surpassed $140 per barrel and phrases such as climate change, carbon footprint, and going green have become fixtures in the daily vernacular. Environmentally ...

Become part of the tremendous growth in medical technology sectors. Learn the basics of medical imaging. Understand regulatory aspects of medical device packaging and miniaturization. Apply principles ...

With Covid accelerating time-to-market for medical devices, digital tools play a key role in managing converging priorities ...

Medical device design and development has evolved over the years, notably influenced by market demands and regulatory requirements. Traditional design practices, beginning with a reliance on generic ...

The integration of optical systems in medical devices is a rapidly growing area of focus and investment within the medical technology sector. From surgical lasers and diagnostic imaging tools to ...

Robert Bubencik, Jr., the president of Eagle Stainless Tube and Fabrication Inc., gave Machine Design an overview of stainless steel instruments at MD&M West 2025. Eagle Stainless, located in Franklin ...

In the unforgiving landscape of medical device development, where regulatory deadlines intersect with clinical imperatives and patient safety requirements, the successful navigation of a 510(k) ...