React expands Luna’s scope beyond SDB
By HME News Staff
Updated 9:50 AM CST, Tue December 13, 2022
SARASOTA, Fla. - React Health has announced 510(k) clearance from the U.S. Food and Drug Administration for the Luna G3 Bilevel S/T 30Vt as a non-invasive ventilator. This expands the utilization of the device beyond the sleep disordered breathing (SDB) market into management of chronic respiratory conditions. “We are pleased the FDA has approved the expanded use of the Luna as a non-invasive ventilator,” said Clint Geffert, president of commercial operations. “React remains committed to the successful treatment of chronic sleep and respiratory diseases and this approval further strengthens our offerings to help improve the lives of millions of patients suffering from these conditions.” Geffert says Luna joins a growing portfolio of respiratory products at React and offers prescribers and providers options at a time when recalls and supply chain challenges have impacted equipment availability. React was formerly 3B Medical.
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