News

Two rival medical device companies specialising in scalp cooling technologies for cancer patients are merging to form a ...
MicroTransponder has posted one-year follow-up data for its FDA-approved device, two months after securing $65m in Series F ...
The IRB has granted approval for FastWave to initiate a coronary feasibility study leveraging its Sola L-IVL system.
Eye health company Bausch + Lomb has received the CE Mark approval in Europe for its LuxLife full range of vision intraocular ...
The National Institutes of Health (NIH) and the Centers for Medicare & Medicaid Services (CMS) are partnering to develop a ...
The US Food and Drug Administration (FDA) has set an "aggressive" timeline to implement genAI across the agency by 30 June ...
GeneDx has completed the acquisition of Fabric Genomics, a US-based company focused on AI-driven human genomic interpretation ...
HeartBeam has secured two new US patents, strengthening its intellectual property (IP) portfolio in cardiac monitoring ...
LumiThera has released new topline data for its Valeda Light Delivery System to slow the progression of dry age-related macular degeneration.
The FDA designation is a step forward for Neuralink as owner Elon Musk faces increasing scrutiny. The US Food and Drug ...
Endogenex has shared results from its REGENT-1 clinical study during the Digestive Disease Week (DDW) 2025 event held in San ...
MedTech reveals that Europeans are generally willing to share their healthcare data in exchange for personalised treatment ...