Abbott/Thoratec Corp. is recalling HeartMate II and HeartMate 3 Left Ventricular Assist System (LVAS) due to an issue called Extrinsic Outflow Graft Obstruction, (EOGO)
Medtronic, has announced launched the Powerease System, an innovative system of electronic instruments designed specifically for use in instrumented or...
Sumitomo has received US FDA 510(k) clearance for its Proton Therapy System, a radiation delivery system for treating Cancerous tissue....
Medtronic plc announced it has received CE Mark approval for the Valiant Navion thoracic stent graft system for the minimally...
The FDA cleared the Flex Robotic System from Medrobotics in July 2015. Now the company has raised $25 million to...
Following the recent CE approval of the Solia S lead for LBBAP (Left Bundle Branch Area Pacing), Biotronik announces the world’s first and only complete CSP system, now fully CE-approved for Left Bundle Branch Area Pacing
Greatbatch has received approval from the FDA for its Algovita Spinal Cord Stimulation (SCS) System to treat chronic intractable pain...
Roche announced the launch of the Digital LightCycler System, Roche’s first digital polymerase chain reaction ( PCR) system
St. Jude Medical has announced FDA approval of the new Proclaim Elite Spinal Cord Stimulation System, an upgradeable and recharge-free...
The FDA has granted Abiomed a 510(k) clearance for an all-in-one, compact cardiopulmonary bypass system called the Abiomed Breethe OXY-1 System.