The device’s continuous monitoring can give doctors an understanding of a person’s condition without the requirement of ...

Scientists from Kaunas University of Technology (KTU), Lithuania, have developed a system for integrated post-stroke ...

British healthtech company Huma Therapeutics has partnered with Eckuity Capital to lay the foundations for an ‘aggressive’ ...

The FDA has awarded 510(k) clearance to Fujirebio’s Lumipulse G pTau 217/β-Amyloid 1-42 Plasma Ratio in vitro diagnostic (IVD ...

Intravascular lithotripsy is quickly gaining the attention of the medtech industry’s giants. Yet distinguishing its true clinical promise from the financial buzz is no easy task.

Implantable lens developer STAAR will fund the repurchase using cash on hand and money generated from business operations.

GE HealthCare has gained 501(k) clearance from the US Food and Drug Administration (FDA) for its CleaRecon DL technology.

Ophthalmic technology developer Intalight has received the CE mark for its DREAM OCT (optical coherence tomography) platform ...

The Final Rule was mooted for implementation over a staged transition period, determined by a service’s risk level, by 2028.

New research has revealed that UK adults feel "let down" by mental health services provided by the UK's National Health ...

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

The FDA has granted breakthrough device designation for Elucent Medical’s EnVisio X1 In-Body Spatial Intelligence System.