Sodium-ion batteries are an interesting alternative to lithium-ion, but they've been held back by complications due to their ...

Lockheed Martin has unveiled a new generation of undersea drones, which it says provides “ technological and strategic ...

Scientists have recognized snails’ regenerative abilities for centuries. In 1766, a researcher documented that decapitated garden snails could regrow their entire heads. Despite that long history, ...

Orthopedics was the most active area over the second half of calendar 2025, with the FDA issuing 13 breakthrough designations to devices in the therapeutic area.

The breakthrough therapy designation, established in 2012 by the US Congress to expedite the development of drugs that show promising early clinical evidence of benefit over available therapies, has ...

CHICAGO (CBS) – Kids and adults need a safe space where they can grow, face their fears, and learn to help others. CBS 2 found just the place called Breakthrough, a social service agency in East ...

The Nest video highlights growing unease around how much control the devices give law enforcement and tech companies.

The Food and Drug Administration (FDA) Breakthrough Devices Program was created by the Congress in the 21st Century Cures Act of 2016. The program is designed to accelerate the development, assessment ...

The technique is called Digital Incoherent Synthesis of Holographic light fields (DISH). Instead of assembling materials layer by layer, DISH projects a three-dimensional holographic light field ...

To date, the global coronavirus disease 2019 (COVID-19) vaccination campaigns have allowed for more than 3 billion doses of the various approved vaccinations to be administered around the world. This ...

John Smith was dead for an hour after falling into a frozen lake, but made a full recovery in a case that even doctors have described as a "bonafide miracle". The incredible true story has been made ...

The Food and Drug Administration Safety and Innovation Act (FDASIA), signed into law on July 9, 2012, introduced several reforms that are intended to streamline the FDA's premarketing approval process ...