LAKE OSWEGO, Ore.-- (BUSINESS WIRE)--BIOTRONIK, a leading manufacturer of cardiovascular medical devices, announced today that the Food and Drug Administration (FDA) has granted approval for its ...

FDA has approved its single- and dual-chamber Entovis pacemakers for use in MRI environments, according to Biotronik Inc. The Lake Oswego, OR-based US subsidiary of Biotronik SE & Co. KG (Berlin) said ...

All new implants should be a fully MRI-compatible system. All new implants should at least be with MRI-compatible leads. No overwhelming need to implant an MRI-compatible device. Based on our daily ...

An electromagnetic therapy for depression shouldn't damage a person's pre-existing implantable cardioverter-defibrillator (ICD), multiple experiments indicated. There was a low risk of ICD damage or ...

LAKE OSWEGO, OR —The US Food and Drug Administration today approved the smallest magnetic resonance (MR)–conditional quadripolar cardiac resynchronization pacemaker available in the US, according to a ...