Investors and analysts are getting antsy as AtriCure awaits word from FDA regarding its Convergent hybrid ablation procedure for atrial fibrillation

Cordis is recalling its Precise Pro Rx US Carotid System because of a risk of separation of the atraumatic distal tip of the sheathed delivery system in patients. There have been seven complaints, including five reported injuries, but no deaths...

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The company expands to offer 600,000 sq ft dedicated to designing, engineering, and manufacturing solutions for minimally invasive surgery and robotic surgery.

The Mountain View, CA-based company has filed the patent complaint with the U.S. International Trade Commission.

In addition to a previously reported HeartWare-related recall, Medtronic is also recalling HeartWare battery cables, data cables, adapter cables, and controller 2.0 Ports.

Medtronic is recalling seven of its implantable cardioverter defibrillators and cardiac resynchronization therapy devices due to an unexpected and rapid decrease in battery life. FDA said there have been 444 complaints about the devices, and 264...

The rates posted by Novitas Solutions, a Medicare Administrative Contractor, are higher than the rate set in late January, but still considerably lower than the reimbursement rate iRhythm was previously receiving for its wearable heart monitoring...