FDA adds five product codes to its premarket notification exemption list, expanding 510(k) exemptions for certain low-risk ...

Survey data shows 57% of U.S. adults own wearables or connected health devices, with 83% wearing them 5+ days weekly, 59% ...

Throughout his tenure at MD+DI, Omar has covered a wide array of topics, including medical technology innovations, regulatory ...

Here’s the list of some of the medical device companies that were slapped with FDA recall notices and corrections in May.

Four competing technologies race to solve radiation therapy's 2.5% range problem. Deep dive into radiacoustic imaging, prompt ...

The world's first dual continuous glucose and ketone monitor is designed to help prevent diabetic ketoacidosis (DKA).

Medtronic reports $36.4B FY26 revenue, up 8.4%, with Q4 beating estimates by $200M. Cardiovascular segment leads with 78% ...

The European Union’s Artificial Intelligence Act is being called one of the most comprehensive AI regulations in the world.

MD+DI Senior Editor Amanda Pedersen shares her experience as a parent whose son received treatment for an eye injury using ...

Federal appeals court reverses $59M Insulet verdict against EOFlow, citing statute of limitations on trade secret claims from ...

Sen. Tom Cotton calls for FDA review of Chinese-made medical devices cleared before 2023 amid rising cyberattacks and patient ...

Abiomed defeats Maquet in patent case over Impella heart pumps, marking second win since 2025—but recalls and FDA issues ...