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

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 ...

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 ...

Buoyed by $110m in funding three months ago, Capstan Medical has reported the first-in-human cases with the mitral technology ...

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 ...

The European orphan drug market is growing and is already comparable in size and scope to the US market. The European Union ...