The US Food and Drug Administration (FDA) has granted 510(k) clearance to Zimmer Biomet's Persona Revision SoluTion Femur.

Vygon claims its bedside monitoring devices can save hospitals thousands per year by cutting out calibration and consumables ...

The US Federal Trade Commission (FTC) has sued to block GTCR’s proposed $627m merger-acquisition of critical medical device ...

Medtronic has announced the SMART trial’s two-year outcomes of Evolut TAVR for aortic stenosis (AS) and small aortic annulus.

The US Food and Drug Administration (FDA) has issued an early alert over a ‘potentially high-risk’ issue with certain Baxter ...

Inari Medical has launched the Artix thrombectomy system, engineered specifically for certain requirements of the peripheral ...

The FDA has granted clearance to Qiagen’s QIAstat-Dx Gastrointestinal Panel 2 Mini B, expanding the company’s syndromic ...

Philips will no longer sell its Tack endovascular system in the US following a Class I recall by the US Food and Drug ...

Vitestro has unveiled Aletta, claimed to be the “world's first” Autonomous Robotic Phlebotomy Device (ARPD), designed for ...

Foresight Diagnostics has launched the PRECISE-HL trial, which will use the Foresight Clarity LDT to treat patients with ...

Closing the gap in health interventions between men and women could add $1tn to the global GDP, unlocking seven additional ...

C Medical Technologies has closed its Series D financing round. which was led by Boston Scientific, raising gross proceeds of ...