Shoulder Innovations has secured $40m in a Series E equity financing round, to mainly progress the commercialisation of ...
Ophthalmology specialist BVI Medical has completed a $1bn capital raise as it positions itself to challenge the might of ...
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.
Traditional screening methods rely on biochemical tests, such as tandem mass spectrometry, which detect metabolic imbalances ...
The US Food and Drug Administration (FDA) has issued an early alert over a ‘potentially high-risk’ issue with certain Baxter ...
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 ...
Inari Medical has launched the Artix thrombectomy system, engineered specifically for certain requirements of the peripheral ...
Post-authorisation safety studies (PASS) are often seen simply as a regulatory necessity, a checkbox that ensures ongoing ...
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