Stanley Bergman has worked at Henry Schein for 45 years, more than 35 of which he spent as CEO, and was due to retire at the ...

Executives at companies innovating a range of new robotic surgery platforms shared their progress and challenges in MedTech ...

The Sapien M3 device is the first approved mitral regurgitation treatment to use a transseptal approach, Edwards said.

The company received three complaints about patients who had perforation injuries linked to the devices.

The Food and Drug Administration clearance and CE mark position Abbott to sell its Amplatzer Piccolo Delivery System in the U ...

The request for information comes as the Trump administration has largely taken a deregulatory stance on AI, in a bid to ...

Abbott can now compete with Medtronic, Boston Scientific and J&J in the U.S. for the fast-growing pulsed field ablation ...

MiniMed is pitching the breadth of its portfolio as an advantage over more focused rivals such as Dexcom and Insulet.

Artificial intelligence has become a buzzword in the medtech industry as more medical devices incorporate the technology. Device companies are using AI to speed up imaging, triage CT scans for serious ...

The Environmental Protection Agency finalized new regulations in March that will enforce tighter regulations on ethylene oxide, one of the most common sterilants for medical devices. The final rule is ...

Employees at the Food and Drug Administration’s medical device center on Tuesday received notice that they would be cut amid massive layoffs at federal health agencies. The reductions included people ...

Michelle Tarver, the new leader of the Food and Drug Administration’s medical device center, faces significant challenges ahead. Patient advocates, who have called for stronger device standards and ...