There is a significant unmet need for novel, effective, and well-tolerated acute migraine treatments. Remote electrical neuromodulation (REN) is a non-pharmacological, non-invasive, acute migraine treatment that stimulates...
The FDA has approved a remote feature for follow-up programming sessions for the Nucleus Cochlear Implant System, from Cochlear Corporation, through a telemedicine platform.
The twelve recommendations are intended to advise physicians on the use of imaging modalities when making a clinical diagnosis, and when to apply imaging for monitoring of disease activity and damage.
The purpose of this study is to determine the efficacy and safety of remote ischemic conditioning for essential hypertension.
Abbott announced that it received approval from the FDA to launch the Liberta RC DBS system, the world's smallest rechargeable deep brain stimulation (DBS) device with remote programming, to treat people living with movement disorders
For the first time, a panel of spinal cord stimulation (SCS) experts has developed best practices in the nascent field of remote SCS device management
Medtronic plc has announced that the FDA has granted 510(k) clearance for its PillCam Small Bowel 3 system for remote endoscopy procedures. The PillCam SB3 @HOME program combines Medtronic's PillCam technology with Amazon logistics, a combination intended to ensure both timely and accurate results for patients from the comfort of their homes.
Biotronik, a leader in cardio- and endovascular medical technology,has announced FDA approval of BioMonitor 2, an insertable cardiac remote monitor...