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

Abbott's REFLECT studies indicate that FreeStyle Libre use is linked to a decrease in hospitalisation risk for heart ...

The US Food and Drug Administration (FDA) has granted approval for Roche's VENTANA MET (SP44) RxDx Assay for NSQ-NSCLC.

A new report by Royal Philips warns that the ‘trust gap’ around deploying artificial intelligence (AI) in healthcare systems ...

The request comes at a time when the medtech industry is facing tariff-induced headwinds of up to $500m in 2025.

Zynex has announced the submission of a 510(k) application to the FDA for its laser pulse oximeter, the NiCO non-invasive ...

Health Canada has granted approval to Subtle Medical’s magnetic resonance imaging (MRI) enhancement software, SubtleHD.

The German multinational joins the long list of companies boosting US manufacturing to counter Trump’s tariffs.

Artificial Intelligence (AI) is now used throughout clinical trials, from recruitment to analysis – but are regulators ...