Edwards’ device, dubbed Sapien M3, is the first approved system to use a transfemoral approach to treating mitral ...

In obtaining CE marking, Avatar Medical strengthens its ... Intended use: Software medical device for examining medical images in 3D format and/or through a virtual reality interface to assist ...

Roche has secured CE mark approval for its immunohistochemistry (IHC) companion diagnostic test, VENTANA FOLR1 (FOLR1-2.1) RxDx Assay, for the identification of epithelial ovarian cancer (EOC ...

“Impulse Dynamics has established leadership and commitment to significantly changing the treatment options available for HF patients,” said Jason Spees, CEO of Impulse Dynamics. “The expanded ...

Elixir trails J&J’s Shockwave but has outpaced Bolt Medical to the European market with its mechanical IVL system.

Medtronic, Abbott and Boston Scientific had updates on their devices used in heart valve disease treatment at the event.

Abbott took "a deliberately very different development path ... for the waveform" behind its Volt PFA system, said Dr.

"Prof. Valmed" was the first company to receive approval from the European Union for its co-pilot of the same name.

Key Milestone Signals Readiness for European Market Entry and Commitment to Quality ExaStim® ExaStim® Stimulation System Los ...

Elixir Medical announced today that it received CE mark for its LithiX hertz contact (HC) intravascular lithotripsy (IVL) ...