The company provided an update on its efforts to win market share, revealing that Maestro has been used to treat over 2,300 ...

The Houston-based startup is developing capabilities for endovascular aneurysm repair and stroke treatment that it hopes can ...

Medtronic and CMR Surgical got the FDA’s green light this month, while SS Innovations applied for clearance. Catch up on the ...

As competition intensifies among surgical robot makers, CMR said its soft tissue platforms are the second most used systems ...

X9 is building an ultrasound-guided device used to simplify the process of inserting a needle for cannulation.

Medicare reimbursement for aortic stenosis patients without symptoms could accelerate procedure growth for Edwards ...

SpectraWAVE makes technologies to help diagnose and guide treatment decisions for coronary artery disease.

Medtech industry groups said the FDA should use existing regulatory and quality tools to monitor performance, while medical ...

Combining pulsed field ablation and a radiofrequency technique in one platform is expected to reduce procedure times.

An FDA warning letter about the wearable company’s blood pressure feature raises questions as the lines between medtech and ...

Companies can ask the FDA to waive premarket authorization and investigational device requirements while they collect ...

FDA's challenges — such as insufficient staffing — can create inefficiencies in the process and potentially put lives at risk ...