The end-stage kidney disease device performed as well in the study as in a pivotal trial that supported FDA approval.

CS Analytical Laboratory, the world's only cGMP, FDA-registered and inspected contract laboratory exclusively designed and ...

The ACC issued new guidance for managing common pediatric left-to-right shunts, including ASD, VSD, and PDA, in the ...

The Vascade MVP vascular closure device. [Image from Haemonetics] Haemonetics (NYSE:HAE) announced today that it received FDA approval to expand the labeling for its Vascade MVP XL system. Expanded ...

MARLBOROUGH, Mass. and NEW ORLEANS, March 28, 2026 /PRNewswire/ -- Boston Scientific Corporation (NYSE: BSX) today announced that the CHAMPION-AF global clinical trial met all primary and secondary ...

Data highlights the WATCHMAN FLX device provided statistically superior protection from bleeding, demonstrated similar efficacy compared to blood thinners in patients with non-valvular atrial ...

Pulmonary haemorrhage (PH) after hybrid ventricular septal defect (VSD) closure has not been documented in the literature and is rarely reported after pulmonary artery debanding. We presented a ...

EL CERRITO — A stretch of San Pablo Avenue in El Cerrito was closed for about an hour Monday after a suspicious device was discovered on a sidewalk, police said. Related Articles Suspected driver in ...