News

The US FDA has granted IDE approval for Dymicron to commence a pivotal trial of its Triadyme-C cervical artificial disc ...
The US Patent and Trademark Office has granted a patent to Geneticure for its genetic test to predict response in renal denervation.
Ablation therapy represents a significant innovation in cancer care. Advanced thermocouple wires are helping to deliver ...
BVI is a winner in the Research and Development, Investments, and Product Launches categories in the 2025 Medical Device ...
ClearNote Health has secured the UK Conformity Assessed (UKCA) marking for the company's Avantect Pancreatic Cancer Test.
The US FDA has approved Boston Scientific’s expanded instructions for use (IFU) labelling of the Farapulse Pulsed Field Ablation (PFA) System.
A court has approved the $305m sale of 23andMe’s assets to a nonprofit led by former 23andMe CEO Anne Wojcicki.
Neuros Medical has raised $56m to support the US commercialisation of Altius direct electrical nerve stimulation system.
Philips has announced the expansion of its collaboration with Medtronic, focusing on advancing patient monitoring ...
The US FDA has granted 510(k) clearance for Exactech’s Equinoxe Scapula Reconstruction System for acromial and scapular spine fractures.
Carmat has filed for insolvency and requested that the Versailles Economic Affairs Court place it in a receivership.
The US FDA has granted 510(k) clearance to PathAI for its digital pathology image management system, AISight Dx.