Abstract: An anti-snoring mouth guard for insertion into a mouth of a user for decreasing snoring and the effects of sleep apnea includes a mouthpiece portion having a bottom wall and a pair of upstanding side walls displaced and opposite one another and extending upwardly from the bottom wall, said mouthpiece having a hemispherical configuration that is complementary to a shape of the user's teeth. Collectively, the bottom wall and pair of side walls define a channel operable to receive teeth of a user's upper pallet. The anti-snoring mouth guard includes tongue depressor portion having a proximal end coupled to the mouthpiece and having a body extending rearwardly at a generally downward angle. A brace may extend between rear ends of the mouthpiece portion and define levels by which the tongue depressor may be inserted such that the tongue depressor may be adjusted vertically and front-to-back.

Abstract: A mandibular advancement splint)MAS) including dentition engagement units, each having a face for operatively abutting a complementary face of the other, and an opposed dentition engagement face which is adapted to positively engage the maxillary or mandibular dentition. A plane of abutment of the faces is approximately normal to the sagittal plane to facilitate sliding displacement of one engagement unit relative to the other. The MAS further includes at least one elastic element configured to operatively exert a user-configurable urging force between said dentition engagement units, so that the mandibular dentition is biased forward and along said abutment plane relative to the maxillary dentition when the splint is in use.

Abstract: The present disclosure provides generally for a therapeutic oral device for sleep apnea and associated methods for using the device. According to the present disclosure, the device may comprise a hard palate portion, mouth guard portion, and a tongue retainer portion. The hard palate portion may comprise one or more materials. The hard palate portion may also comprise a composite of materials, including but not limited to embedded materials. The mouth guard portion may comprise one or more components that provide stability and maintain the position of the therapeutic oral device within the mouth. The tongue retainer portion may comprise an airway and a predetermined length. A method of use may comprise the utilization of one or more incremental oral devices to overcome a gag reflex. When the oral device is formed from a mold, the mouth guard portion and the hard palate portion may be custom fit to the dimensions of the intended mouth.