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 ...

LumiThera has released new topline data for its Valeda Light Delivery System to slow the progression of dry age-related ...

The US Food and Drug Administration (FDA) has set an "aggressive" timeline to implement genAI across the agency by 30 June ...

A new AI model will be trained on a large set of NHS data in hopes of identifying early interventions for patient care.

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 ...

MedTech reveals that Europeans are generally willing to share their healthcare data in exchange for personalised treatment ...

The company slashed its 2025 earnings forecast due to the ongoing financial fallout from the US-China tariffs.

Endogenex has shared results from its REGENT-1 clinical study during the Digestive Disease Week (DDW) 2025 event held in San ...

BrightHeart has gained a further 510(k) clearance from the FDA for its AI-based prenatal congenital heart defect (CHD) ...

Health Canada has approved Merit Medical Systems’ Wrapsody cell-impermeable endoprosthesis (CIE) device for haemodialysis ...