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

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

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

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

Teleflex (NYSE: TFX) + Teleflex Incorporated $121.59 0.16% Open 118.41 Day High 124.024 52 Week High 257.04 52 Week Low ...

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

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

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

Field Medical announced today that it has closed a Series B funding round worth proceeds totaling $35 million.

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

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

Moon Surgical today announced it received FDA 510(k) clearance for two new features on the Maestro robotic surgical assistant ...