MedTech News
U.S. Food and Drug Administration Gives Huxley Medical 510(k) Clearance for SANSA Home Sleep Apnea Test
ATLANTA, Aug. 7, 2024 /PRNewswire/ — Huxley Medical, a developer of technologies that streamline cardiopulmonary care, has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for its groundbreaking, chest-worn, sleep apnea diagnostic patch, SANSA.
Natus introduces autoSCORE, an innovative AI solution capable of a new era of expert-level clinical EEG interpretation
MIDDLETON, Wis., Aug. 7, 2024 /PRNewswire/ — Natus Medical Incorporated has announced the launch of autoSCORE, the first-of-its-kind artificial intelligence model capable of automatic and comprehensive clinical EEG interpretation, providing accuracy on par with medical experts.
How supercharged silk could help heal the heart
UNSW researchers have developed a new microgel made of moth silk that is designed to assist with tissue regeneration and could help people recover from heart attacks.
Electric bandage holds promise for treating chronic wounds
Researchers have developed an inexpensive bandage that uses an electric field to promote healing in chronic wounds
Researchers develop a new vaccine additive that creates a stronger, tunable immune response
Researchers at Stanford Engineering have developed a nanoparticle platform that could make existing vaccines more effective, including those for influenza, COVID-19, and HIV.
Karl Storz’s AventaMed wins FDA nod for ear tube placement device
AventaMed, a Karl Storz company, announced that it received FDA 510(k) clearance for its Solo+ ear tube placement system.
Medtronic wins FDA nod for next-gen Simplera CGM
Medtronic (NYSE: MDT)+ got another boost for its CGM portfolio, adding to the collaboration with Abbott announced today.
Johnson & Johnson MedTech Announces Labeling Amendment of LINX™ Reflux Management System in the U.S.
CINCINNATI, OH August 7, 2024 – Ethicon*, a Johnson & Johnson MedTech company**, announced today that the U.S. Food & Drug Administration (FDA) has approved a label update to expand the availability of the LINX™ Reflux Management System to include patients with Barrett’s esophagus (BE) experiencing gastroesophageal reflux disease (GERD) symptoms.