The Magazine for Sleep Professionals
Friday, July 31, 2026
Michigan Instruments is excited to introduce the Spontaneous Breathing Lung (SBL™)! The new and improved way to create spontaneous breathing with accurate stimulation of a breathing patient. Spontaneous breathing simulations are useful for testing, designing, and training on non-invasive and supportive modes of ventilation, as well as oxygenation. The SBL […]
Somnoware, the leading cloud-based platform for enhanced respiratory care management, announces the release of its Fax Intake Module. The Fax Intake Module transforms paper-based faxing into an all-digital experience. The module streamlines the fax intake process with easy-to-use functionality for patient referrals. “Somnoware’s intake module eliminates paper processes, saves time, and reduces […]
Nihon Kohden OrangeMed, Inc. received U.S. Food and Drug Administration (FDA) 510(k) clearance for its NKV-330 Ventilator System. The NKV-330 is a non-invasive ventilator that provides respiratory support to adult and pediatric patients. It offers not only non-invasive ventilation but also invasive ventilation as well as high-flow oxygen therapy. In […]
The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death. Recalled Product Product Name: SafeStar 55 Breathing System Filter Product Model Numbers: MP01790 Lot Number: LT2103 Devices Recalled in the U.S.: 35,950 Dates distributed: […]
Nyxoah SA announced that the U.S. Food and Drug Administration (FDA) has approved the use of Nyxoah’s next-generation Genio® 2.1 system for use in the Company’s DREAM U.S. IDE pivotal study. Genio® 2.1’s upgrades are entirely related to the external components of the Genio® system, as the implantable stimulator remains […]
LivaNova PLC has announced the first patient implanted in the investigational device exemption (IDE) clinical study, “Treating Obstructive Sleep Apnea using Targeted Hypoglossal Neurostimulation” (OSPREY). The randomized controlled trial (RCT) seeks to demonstrate the safety and effectiveness of the LivaNova aura6000™ System, an implantable hypoglossal neurostimulator intended to treat adult patients with […]
WatchPAT® with SleePATh® is a digital solution for clinicians which integrates automated subjective patient data with the WatchPAT® ONE home sleep study results for enhanced diagnosis, data management and analysis. It simplifies the patient journey, streamlines the clinical experience and enhances the diagnosis. It combines pre and post sleep study […]
Turn Medical has launched its first product, a prone positioning device, the Pronova-O2™ Automated Prone Therapy System. Substantial research has demonstrated the benefits of prone positioning for critically ill patients with respiratory distress. The Pronova-O2™ System provides an effective and efficient way for clinicians to move patients into the prone position and maintain […]
Masimo has announced Dual SET® Pulse Oximetry for Root®, a highly versatile patient monitoring and connectivity hub. The first application of Dual SET® Oximetry is a significant advancement to Masimo SET®-guided critical congenital heart disease (CCHD) screening, with the CE marking and European launch of the Masimo SET® MOC-9® module and the addition of […]
SoClean Inc. has filed a federal lawsuit in the United States District Court for the District of Massachusetts against Philips. According to the complaint, Philips has misled the public and engaged in acts of deliberate misdirection, placing blame on SoClean to divert attention away from obvious design flaws, including a poor choice […]
