Shoulder Innovations has secured $40m in a Series E equity financing round, to mainly progress the commercialisation of ...

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

Ophthalmology specialist BVI Medical has completed a $1bn capital raise as it positions itself to challenge the might of ...

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.

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

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

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

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

Post-authorisation safety studies (PASS) are often seen simply as a regulatory necessity, a checkbox that ensures ongoing ...

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

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