Philips has announced it received FDA 510(k) clearance for its deep-learning reconstruction tool, SmartSpeed Precise.

The FDA alerted providers that Abiomed issued updated instructions for use related to all of its Automated Impella ...

CE mark represents the latest recent regulatory milestone for Intuitive. In May, the company won FDA clearance for a new ...

Kardium announced today that it raised $250 million in a new financing round to support the launch of its pulsed field ...

Philips (NYSE:PHG) and Medtronic (NYSE:MDT) today announced an expansion of their longstanding partnership with a multi-year ...

MiRus announced new early feasibility study results supporting the use of its Siegel transcatheter aortic valve replacement ...

Fasikl announced that it received FDA 510(k) clearance for its first-of-its-kind NeuroAI wristband for essential tremor.

Acutus announced at the end of 2024 that it planned a realignment of resources and operational downsizing. The company ...

CroíValve announced today that it received new funding from Horizon Europe’s European Innovation Council (EIC) Accelerator ...

Teleflex (NYSE: TFX) announced that it completed its previously announced acquisition of the Biotronik (VI) business.

Stereotaxis (NYSE:STXS) announced the publication of initial clinical results using its MAGiC robotic magnetic navigation ...

Onward Medical announced today that it submitted its ARC-EX system for expanded FDA indication and for CE mark approval.