A dental intraoral device that is worn within an oral cavity, the dental intraoral device comprising a resin tooth portion. At least a part of the tooth portion is formed into a mesh shape. The part of the tooth portion is preferably formed by approximately regularly arranging unit regions having holes.

A method to facilitate the growth of desired bacteria in a human's mouth by using a bioadhesive strip that has an encapsulated feature containing at least one bacteria that has one of a pathogenic or toxic element excised using a clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR associated protein (Cas) system or a CRISPR from Prevotella and Francisella 1 (Cpf1) system, and in particular, using oral strips that adhere to surfaces in the oral cavity and that include at least one of xylitol, Lachnospira, Veillonella, Faecalibacterium and/or Rothia bacteria.

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.

An edentulous mouth insert appliance for mounting upon the edentulous gum of a patient, comprises a u-shaped frame formed of a rigid flexible material, with a portion to embrace the gum and a portion extending beyond the gum with an exposed surface to replicate a bite aligned with the corresponding occlusal plane. The frame has a base supporting a pair of inner and outer side walls spaced apart by the base a distance allowing the frame to encircle and cover the edentulous gum with a space between inner surfaces of the frame and the gum. A fill within the frame fills the space between the frame and the gum upon which the appliance is fitted, providing a void-free seal between the apparatus and the gum.

Example embodiments of the present invention provide a multi-function oral appliance, comprising an elastomeric polymer, a hard non-elastic polymer, or a combination of the two fused together; formed using 3D printing or vacuum-forming; configured to engage all or part of the bottom and top teeth such that the lower jaw is advanced, e.g., 8 mm, anterior to its habitual resting position and opened, e.g., 8 mm, from its habitual resting position when the appliance is applied; and configured such that, e.g., 90%, or more, of airflow through the mouth is blocked by the appliance. In some embodiments, the appliance is configured to include gel-wells in the interior of the appliance.

A device including one or more preformed or customized eruption guidance appliances placed in an individual's mouth. The preformed appliances are vibrated with a pulsation device to encourage tooth eruption by increasing the force and efficiency of the eruption toward a preferred location and a preferred alignment as well as providing increased blood flow and blood oxygen flow to the muscles and tissues in and around the oral cavity of the individual. The preformed guidance appliance driven by the pulsation device is selected from a range of guidance appliances, each of which is selected by size and shape to fit an individual based on the individuals anticipated tooth and jaw size as well as the growth profile. The pulsation can increase the blood and oxygen flow to the many muscles that surround the appliances outside surfaces that can alter mouth breathing, prevent impingement of the oropharynx from the abnormal distalization of the tongue and mandible during sleep, the proper resting posture of the tongue, increased nasal breathing, prevent snoring, improve abnormal swallowing, correct thumb sucking and various abnormalities of speech.

Oral appliances that may include a supporting shell member having concave geometry for receiving at least a portion of a dental arch of a wearer into the concave geometry; and, a tongue guide member extending from said supporting shell member and into contact with an underside of a tongue of said wearer when the portion of the dental arch is received into the concave geometry. This oral appliance may be utilized in methods for treating various sleep and breathing disorders (“SBD”), for treating sleep apnea, treating airway obstruction, for upper and/or lower jaw reshaping, for airway reshaping, for mandibular advancement, for tongue-retaining, and for providing myofunctional therapy to encourage and help train the tongue to have the proper tongue posture for nasal breathing and discourage mouth breathing.

The diagnosed soft tissue or brain injury component of concussions is generally defined by the symptoms of the temporal lobe manifestations. However, there is an undiagnosed structural fractured component of concussions occurring within the jaw joint complex which is the focus of this invention. A precise imaging technique and the powerful 3D Cone beam scanning technology, together, have revealed fractures in temporal bones of the jaw joint space which supports the temporal lobe of the brain. These fractures are the results of the lower jaw impact forces that cause concussions and this mechanism account for a large percent of the concussions arising in sports and military operations. These fractures have never been considered, diagnosed, or treated in the management of concussions. Fracturing temporal bones in the jaw joint that supports the temporal lobe will certainly produce the symptoms of temporal lobe manifestations. With early detection, these fractures can be more rapidly healed, eliminating many temporal lobe symptoms of concussions. The device of the present invention reduces the risk of the lower jaw impact concussion and temporal bone fractures, while enhancing the ability to speak and orally communicate.