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Seismic Shifts in the Sleep Therapy Landscape

Tremblors from the Philips CPAP recall continue to shift the therapy landscape in sleep medicine. Impacts and a potential silver lining.

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ProSomnus Reports Successful Pilot Study Validation of Next Generation Remote Patient Monitoring Device for Obstructive Sleep Apnea

PLEASANTON, Calif., Feb. 22, 2024 ProSomnus, Inc. , the leading non-CPAP Obstructive Sleep Apnea therapy™, announced results of its pilot study for the Company’s Next Generation Remote.

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ProSomnus 510(k) Submission Under Review for Severe Indication

The FDA is in the process of reviewing ProSomnus' premarket notification for its ProSomnus EVO oral appliance for severe sleep apnea.

Len liptakJohn remmersDrug administrationProsomnus inc

ProSomnus Poised to Support Obstructive Sleep Apnea Patients Following Discontinuation of Philips Respironics OSA Devices

PLEASANTON, Calif., Jan. 29, 2024 ProSomnus, Inc. , the leading non-CPAP Obstructive Sleep Apnea therapy™, announced that the company is well-positioned to support patients with OSA and.

United statesLen liptakHeather whalenMarkt murphyPhilips respironicsKent smithMike cavanaughExchange commissionSecurities exchangeCompany annual report on formDrug administrationProsomnus incSleep apneaObstructive sleep apneaChief executive officerDental sleep medicine

Philips discontinues certain CPAP product lines after recall saga

Philips has discontinued several respiratory device product lines, including one from its much-maligned CPAP portfolio.

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