The U.S. Food and Drug Administration (FDA) categorizes medical devices into three classes based on the level of risk the devices pose to patients and users. Image Credit: IGORdeyka/Shutterstock.com ...

A new display prototype for high-end medical equipment employs a simple and highly resistant technology to incorporate a permanent status indicator; it serves as an additional safety feature by ...

A medical device is any appliance, apparatus, software, material, or other articles, which may be used in isolation or combination (as defined by the manufacturer) by individuals for a medical purpose ...

In conversations about medical device cybersecurity, attention focuses on the Food and Drug Administration’s (FDA) rules and guidelines. With a refresh in 2023 that emphasized new protocols for ...

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 ...

Fueled by convenience, fashion, size and technical innovation, medical devices have evolved from clinical settings to daily consumer use. Today’s highly personalized devices are being embedded into ...

Ahead of Display Week 2025, CEO Robert Ramsey, Ph.D., and Chief Scientist Michael Robinson, Ph.D., of Rain Technology today shared domain expert commentary and video explainers about the future for ...

The medical device contract manufacturing industry is continuing to transform through 2024. A decade before COVID highlighted the critical nature of manufacturing infrastructure, there were investors ...

Medical device lifetime expectancy is currently a hot topic in the industry, given the European medical device regulations requirement, EU MDR 2017/745, Article 18 1(c). Article 83 Post Market ...

The Food and Drug Administration (FDA) development and approval process for drugs and medical devices involves multiple phases that ensure the safety and effectiveness of products before and after ...