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2. Tasimelteon - Wikipedia

   en.wikipedia.org/wiki/Tasimelteon

   Tasimelteon, sold under the brand name Hetlioz, is a medication approved by the U.S. Food and Drug Administration (FDA) [3] in January 2014, for the treatment of non-24-hour sleep–wake disorder (also called non-24, N24 and N24HSWD). [4]

3. Hypoglossal nerve stimulator - Wikipedia

   en.wikipedia.org/wiki/Hypoglossal_nerve_stimulator

   Certain patients with obstructive sleep apnea who are deemed eligible candidates may be offered the hypoglossal nerve stimulator as an alternative. FDA-approved hypoglossal nerve neurostimulation is considered medically reasonable and necessary for the treatment of moderate to severe obstructive sleep apnea when all of the following criteria are met: [4]

4. What to Do If You Have Sleep Apnea - AOL

   www.aol.com/sleep-apnea-182844308.html

   Sleep apnea and CPAP. Although CPAP machines work well for tens of millions, many other people struggle with them. Some of these challenges can be addressed with the right guidance and strategies.

5. Sleep apnea: causes, symptoms, treatments, and how it ... - AOL

   www.aol.com/lifestyle/sleep-apnea-causes...

   "To diagnose sleep apnea on a home or in-lab sleep test, we count the number of disturbances in a patient's breathing and divide it by the amount of time they slept to come up with a per-hour ...

6. Melatonin receptor agonist - Wikipedia

   en.wikipedia.org/wiki/Melatonin_receptor_agonist

   The Food and Drug Administration (FDA) granted tasimelteon orphan drug designation status for blind individuals without light perception with non-24-hour sleep–wake disorder in January the same year, [citation needed] and final FDA approval for the same purpose was achieved in January 2014 under the trade name Hetlioz. [10]

7. FDA clears Tyler company’s device to treat obstructive sleep ...

   www.aol.com/fda-approves-tyler-company-device...

   The AIO Breathe Device is a “new mandibular repositioning device” that was designed by local sleep physician Dr. Raghavendra V. Ghuge, MD, MBA, DABSM, […] FDA clears Tyler company’s device ...