The end of an earnings season can be a great time to discover new stocks and assess how companies are handling the current ...

Medtech developers incorporating AI or machine learning into medical devices need to recognize if and how FDA will regulate ...

Medical device equipment manufacturers work in an environment where product quality isn't just a competitive advantage, it's a regulatory necessity with direct implications for patient safety. As ...

Food and Drug Administration (FDA) regulations mandate that all medical device vendors tighten their security features with processes to find and mitigate vulnerabilities. The FDA mandate is a step in ...

Ransomware attacks on the healthcare sector surged by 30 percent in 2025, frequently disrupting operational technology and medical devices. FDA Section 524B mandates that manufacturers provide a ...

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 ...

Implantable medical devices are introduced into the human body through surgery or other medical interventions to serve specific functions. The most common examples of implantable medical devices ...

Multiple sclerosis (MS) can affect a person’s vision, balance, muscle strength, and coordination. Some assistive devices, such as wheelchairs, canes, and motorized scooters, can help improve mobility ...

The World Health Organization (WHO) states that over 2.5 billion people worldwide use assistive devices, and that number is likely to rise as the older population grows. Older people face unique ...