Unlike clinical-grade stimulators that require medical supervision or invasive procedures, Pulsetto is positioned within the ...

Neosoma, Inc. is excited to announce that it has received FDA 510(k) clearance for its Brain Mets software medical device. This clearance ushers in a new era in the assessment of brain metastases, ...

Women’s health neurotechnology applies brain stimulation using a wearable to PMS, menstrual pain, and mood—addressing gaps ...

SN Bioscience Inc. (CEO Young Hwan PARK) announced that the FDA had granted Orphan Drug Designation (ODD) on December 10 for gastric cancer (including gastroesophageal junction cancer) to SNB-101 (API ...

Twenty-six letters, twelve months, and more plot twists than a season finale. That was 2025 in technology—a year when Chinese ...

Introduction This article outlines the research protocol for a multicentre, randomised, controlled study designed to evaluate the therapeutic effect of a modified olfactory training (MOT) based on ...

The Sapien M3 device is the first approved mitral regurgitation treatment to use a transseptal approach, Edwards said.

Edwards Lifesciences announced today that its Sapien M3 mitral valve replacement system received FDA approval for mitral ...

Imagine a world where hackers can easily hijack the software controlling a ventilator or breach patient data. The ...

The Department of Health and Human Services (HHS) just issued a major Request for Information (RFI) on artificial intelligence in clinical care. Comments are due February 21, 2026. It is led by the ...

Two proposed rules released Monday would pare back government guardrails around health information technology software, including some put forward by the Biden administration.