A lip sealing tape for preventing a user's mouth from opening in daily life and during sleep is proposed. The lip sealing tape adds a mouth-closing vector to assist a vector that displaces a position of a user's tongue forward and upward, thereby forming a closed vector system of muscles of the entire body to increase physical stability and induce nasal respiration (breathing through a user's nose) to gradually reduce oral respiration while promoting nasal respiration. The lip sealing tape is characterized by simply adding the mouth-closing vector to prevent opening of the user's upper and lower lips, by means of horizontal and vertical adhesive tape portions, thereby minimizing a contact area with a user's facial skin when worn and thus minimizing discomfort due to stuffiness while maximizing safety when worn.

An oral training appliance for training the tongue and lips of a person is disclosed. The appliance comprises a U shaped body comprising a front section and two arms, an inner wall and an outer wall. A tongue training member extends from the inner wall and is moveable in response to movement by the user's tongue from a rest configuration to a training configuration. The appliance also comprises a lip training member and is moveable in response to movement of a user's lower lip from a rest configuration to a training configuration and the lip training member is biased towards the rest configuration.

An oral orthotic device includes a body having a left portion including an upper surface and a right portion including an upper surface. The upper surface of the left portion and the upper surface of the right portion define a plane positioned to extend above an irregular surface defined by teeth of a user. A bite block extends from the upper surface of one of the left portion or the right portion a distance above the plane such that the bite block is disposed on the oral orthotic device exclusively on either the left portion or the right portion. One or more springs extend from the body and are configured to buffer the body from the teeth of the user. A lingual portion is coupled to the left portion of the body and to the right portion of the body. The lingual portion encloses a helical wire.

A medical appliance for the treatment of one or more sleep disorders such as obstructive sleep apnea in a patient, the appliance comprising: a biasing member for inserting behind and exerting a force upon the patient's soft palate or tongue, wherein the biasing member is inserted in a reduced or minimized form and then expanded or firms once in place to exert the force. The appliance may be nasally inserted or be placed through the mouth. In a particular configuration, both the soft palate and tongue are biased to prevent obstruction of the flow of air in the nasopharyngeal airway.

A medical appliance for the treatment of one or more sleep disorders such as obstructive sleep apnea in a patient, the appliance comprising: a biasing member for inserting behind and exerting a force upon the patient's soft palate or tongue, wherein the biasing member is inserted in a reduced or minimized form and then expanded or firms once in place to exert the force. The appliance may be nasally inserted or be placed through the mouth. In a particular configuration, both the soft palate and tongue are biased to prevent obstruction of the flow of air in the nasopharyngeal airway.

An anterior guidance package (AGP) including: a mandibular guidance component attachable to a mandibular retentive piece configured to be placed about a mandibular arch of a user; and a maxillary guidance component attachable to a maxillary retentive piece configured to be placed about a maxillary arch of a user, the maxillary guidance component configured to mate with the mandibular guidance component for guiding a movement of the mandibular guidance component relative to the maxillary guidance component, wherein the mandibular guidance component is maintained in a correct orientation relative to the maxillary guidance component.

Embodiments described herein to a device for improving respiration comprising at least one nasal insert provided to be inserted into a nostril of a user, wherein the at least one nasal insert comprises a conical base body, a through-hole extending along the main axis of the base body, and a spiral element arranged on the inside of the base body and extending from the base of the base body to the tip of the base body.

A device and method for creating and/or maintain an obstruction free upper airway passage. The device configured to fit under the chin of a subject adjacent to the subject's at an external location corresponding approximately with the subject's internal soft tissue associated with the neck's anterior triangle. The device including structural elements designed to optimize comfort, compliance and seal achieved through minimizing the pressure variation along the contact surface of the cushion element. The structural elements of the cushion may include a fluidly sealed chamber that may vary in thickness and width, a compressible elastic foam contained within the fluidly sealed chamber a ribbon layer backing the elastic foam contained within the fluidly sealed chamber and an adhesive layer disposed on the outer surface of the fluidly sealed chamber of the therapy device designed to contact the skin of the subject.

A device and method for creating and/or maintain an obstruction free upper airway passage. The device configured to fit under the chin of a subject adjacent to the subject's at an external location corresponding approximately with the subject's internal soft tissue associated with the neck's anterior triangle. The device including structural elements designed to optimize comfort, compliance and seal achieved through minimizing the pressure variation along the contact surface of the cushion element. The structural elements of the cushion may include a fluidly sealed chamber that may vary in thickness and width, a compressible elastic foam contained within the fluidly sealed chamber a ribbon layer backing the elastic foam contained within the fluidly sealed chamber and an adhesive layer disposed on the outer surface of the fluidly sealed chamber of the therapy device designed to contact the skin of the subject.

A breathing sound measurement device includes a measurement section configured to be brought into contact with a skin of a front neck of a subject and measure breathing sound of the subject and a wearing section configured to have a first end connected to the measurement section and have elasticity to extend in a circular arc shape along an outer circumference of the subject's neck. The wearing section has a second end provided with a pressing portion configured to be pressed against a skin of a rear neck opposite a right front neck with respect to a midpoint between right and left halves of the subject's neck.