Articles related to MEDICAL DEVICES

Hypoglossal nerve stimulation, a newer surgical option for obstructive sleep apnea, shows high adherence and durable benefits, significantly reducing AHI and improving patient outcomes.

The FDA has recalled Abbott’s HeartMate 3 LVAD after reports of severe complications during implantation, including blood leakage and air entry, which can lead to serious surgical risks.

Nozomi Networks Labs identified 11 cybersecurity vulnerabilities in GE Healthcare’s ultrasound devices, posing significant risks to patient data and medical equipment functionality. Mitigation strategies are crucial to safeguard against potential attacks.

A case of pacemaker-lead dislodgement with cardiac perforation in a 96-year-old patient highlights the importance of recognizing and addressing complications swiftly to prevent severe outcomes.

Explore the FDA-cleared Modius Stress, offering groundbreaking ease in managing generalized anxiety with daily 30-minute sessions, showing significant reductions in GAD-7 scores in international clinical trials.

Philips Respironics has established a consent decree with US regulators to ensure the safety and compliance of their sleep and respiratory care devices, focusing on stringent remediation and continued patient support amidst ongoing sales restrictions.