FDA Awards Marketing Clearance to Restorative Therapies’ Xcite FES System January 18, 2017 The device promotes movement in neurologically-damaged appendages via electrical stimulation. Read More
Medtronic Wins CE Mark for 34mm Heart Valve January 18, 2017 This valve was designed for patients with severe aortic constriction who have large arteries. Read More
FDA Grants Marketing Clearance to CyMedica Orthopedics’ Wireless Muscle Stimulation Device January 18, 2017 The device can be controlled with your smart phone. Read More
Medasense Biometrics Nabs CE Mark for Pain Monitoring System January 18, 2017 This device is used to measure efficiency of analgesics. Read More
FDA Clears SpineGuard’s DSG Integration Module to Market January 17, 2017 A DSG-enabled screw is a combination of a bipolar sensor and a pedicle screw in one device. Read More
MindChild Medical Acquires FDA Marketing Clearance for Fetal Monitoring System January 17, 2017 The device externally measures fetal heart rate, maternal heart rate and uterine contractions. Read More
European Union Grants CE Mark for Intact Vascular’s Tack Endovascular System January 17, 2017 The device can be used in arteries ranging from 1.5 mm to 4.5 mm in diameter. Read More
Ventripoint Submits Application to Health Canada for Complete Heart Analysis System January 17, 2017 The product is already licensed in Canada for use for the right ventricle. Read More
Abbott Launches EnSite Cardiac Mapping System with Catheter Attachment January 13, 2017 The device system allows physicians to map heart chambers with any electrophysiology catheter. Read More
Philips Reveals Augmented-Reality Surgical Navigation Technology January 13, 2017 The technology uses cameras mounted on a flat panel X-ray detector. Read More
Final Guidance Addresses Medical Device Cybersecurity Reports January 13, 2017 Companies must report of vulnerabilities within 30 days and eliminate it within 60 days. Read More
Cures Act Encourages Breakthrough Devices, Exempts Medical Software January 13, 2017 To participate in the program, a device must offer significant advantages over existing products. Read More