1883 results about "Mouth opening" patented technology

A protective cover for a device having a touch-sensitive screen, the cover being a substantially optically transparent flexible protective cover formed of a unitary combination of a mask portion substantially surrounded with a plurality of integrally interconnected curtain portions extending therefrom and forming therebetween a plurality of interconnected lip portions, the mask, curtain and lip portions forming a cavity therebetween with the lip portions surrounding a mouth opening thereinto; and the mask portion further having a relatively thicker frame portion surrounding a relatively thinner recessed integral window portion formed of a flexible membrane that is positioned over the device's touch screen.

A protective cover for a device having a touch-sensitive screen, the cover being a substantially optically transparent flexible protective cover formed of a unitary combination of a mask portion substantially surrounded with a plurality of integrally interconnected curtain portions extending therefrom and forming therebetween a plurality of interconnected lip portions, the mask, curtain and lip portions forming a cavity therebetween with the lip portions surrounding a mouth opening thereinto; and the mask portion further having a relatively thicker frame portion surrounding a relatively thinner recessed integral window portion formed of a flexible membrane that is positioned over the device's touch screen.

A device for directing a liquid onto a plurality of surfaces of the oral cavity, the device including a chamber for maintaining the liquid proximate the surfaces, where the chamber is defined by front, rear and base inner walls of the device and the front and rear inner walls each include a plurality of openings, the devices further including a first manifold and a second manifold, a first port and a second port; and means for providing an effective seal of the device within the oral cavity.

A medical instrument includes an elongate tubular introducer member, an elongate slider member disposed at least partially inside the tubular member, a loop provided at a distal end of the slider member, a pouch connected to the loop so that the loop defines a mouth opening of the pouch and so that the pouch is slidable along at least a proximal portion of the loop, and a tether connected to the pouch at a proximal side thereof. The tether extends into the tubular member and is fastened to the tubular member at a location spaced by a distance from a distal tip of the tubular member. The tether has a length from the fastening location to the pouch that is less than the distance between the location and the tip of the tubular member.

A method of placing a dental implant analog in a physical model for use in creating a dental prosthesis is provided. The physical model, which is usually based on an impression of the patient's mouth or a scan of the patient's mouth, is prepared. The model is scanned. A three-dimensional computer model of the physical model is created and is used to develop the location of the dental implant. A robot then modifies the physical model to create an opening for the implant analog. The robot then places the implant analog within the opening at the location dictated by the three-dimensional computer model.

A magnetic oral retractor assembly for distending the cheek of a patient undergoing an oral dental / surgical procedure comprises a gripper element mounted to a support structure external of the patient's oral cavity and an intraoral retractor device for contacting the inner surface of the patient's cheek. The gripper element and the retractor device each include a magnetic member, at least one magnetic member being a magnet and the other being either another magnet or a non-magnetized magnetically permeable member. The magnetic members are positioned on the gripper element and the retractor device for magnetically coupling the gripper element to the retractor device through the patient's cheek. The invention has application in surgical procedures to secure patient tissue magnetically in place during surgical procedures or to distend an opening in a patient's body wall during an open surgical procedure.

A medical cauterization snare includes a tubular member such as a catheter, a rod or wire disposed at least partially inside the tubular member, and a resilient loop of a first size attached to a distal end of the rod or wire. The loop includes a nose on a side of the loop opposite the wire. The loop further includes two loop sections each extending between the wire and the nose. The loop sections are each formed with a respective notch or dent for enabling a use of the loop in a second size smaller than the first size. Positioning the loop relative to the tubular member so that the notches or dents are disposed at a mouth opening of the tubular member generates this secondary deployment configuration.

Apparatuses and processes for aperturing and stretching a web are disclosed. In one embodiment, the method involves feeding a web into a nip that is formed between at least one pair of intermeshing rolls. The first roll is a raised ridge rotary knife aperturing roll and the second roll is a ring roll; both rolls comprise ridges and grooves. The first roll comprises a plurality of spaced-apart teeth extending outwardly from the top surface of the ridges, said teeth having tips, wherein the top surface of said ridges are disposed between the tips of said teeth and the bottom surface of said grooves. These apparatuses and processes enable a web to be formed which comprises apertures having greater open area than previously achievable with traditional processes and apparatuses.

A pinch bottom open mouth bulk material bag fabricated from polywoven material has closures at one or both ends that are non-sewn and which comprise a strip of tape running in the cross-bag direction. The tape is folded over the respective bag end, which may be modified, and is glued in place to close the end. The closure has no holes or other openings through which contaminants may enter the bag interior.

A nasal mask assembly that includes a seal member defined from a unitary piece of elastomeric material. The seal member defines a nose receiving cavity and has a first end portion and a second end portion generally opposite the first end portion. A first opening in the first end portion allows at least a portion of a nose to enter the nose receiving cavity such that the nares of the patient communicate with the nose receiving cavity. The seal member includes a neck portion defined in the second end portion and a second opening defined in the neck portion in communication with the nose receiving cavity. A reinforcement area is provided on the side walls of the seal member. The reinforcement area comprises a saddle shaped contoured area on each side of the seal member. Each saddle shaped area has an upper and a lower protrusion portion for providing supporting contact with the face.

A vacuum grooming tool is disclosed that includes a vacuum nozzle attachable to a vacuum source and has a hollow body with a mouth opening. A grooming device selected from a variety of standard animal grooming hand tools, such as a shedding blade, rake, or de-matting tool, may span the mouth opening. The grooming device is positioned such that the airflow created by the vacuum source flows over at least one side of the grooming device. A vacuum cleaning tool for removing any animal hair from a grooming tool is also disclosed. A vacuum plenum of the cleaning tool is attachable to a vacuum source and has an opening for cleaning the grooming tool in one pass. The cleaning tool can be mounted on a stationary support and may also include a pivot-action mechanism that connects the vacuum grooming tool or the cleaning tool to the vacuum source.

A nasal dilator comprises a laminate of vertical layers each consisting of one or more members or components. The laminated layers form a unitary, or single body, truss featuring horizontal regions adapted to engage outer wall tissues of first and second nasal passages and to traverse the bridge of a nose therebetween. When in use the dilator acts to stabilize and / or expand the nasal outer wall tissues and prevent said tissues from drawing inward during breathing. The dilator includes means to direct its resilient properties comprising one or more interior or exterior material separations, or discontinuity of shape of material, formed in at least one region of the truss and extending through at least one layer of the dilator. Said material separation or discontinuity of shape may comprise an opening, relief cut, slit or notch, and which may be configured to separate or vertically protrude, in part, from the truss when the dilator is in use on the nose of a wearer. Said separation or vertical protrusion changes the angle of focused delaminating spring biasing forces generated by the resilient layer, transforming said forces, at least in part, from primarily peel forces into primarily shear forces, and further redistributing or imparting said transformed forces to tissue engaging surface areas extending outward and beyond said material separation.

A nose hair trimmer with dual cutting edges which comprises a stationary blade with a plurality of teeth disposed on two opposite longitudinal sides thereof; a movable blade with a plurality of teeth disposed on two opposite longitudinal sides thereof, and the movable blade is driven by a driving unit to move in a linear reciprocating manner against the stationary blade so that the teeth on one side of the stationary blade and the teeth on one side of the movable blade cooperate with each other to define a first cutting edge, and the teeth on the other side of the stationary blade and the teeth on the other side of the movable blade cooperate with each other to define a second cutting edge; and a casing having a head portion in shape and size adapted to be inserted into a human nose, and the head portion is provided with two longitudinal openings disposed opposite to each other for exposing the first cutting edge and the second cutting edge respectively, so that the first cutting edge and the second cutting edge are positioned substantially parallel to a longitudinal axis of a nasal passage of a human nose when the head portion is inserted into the nose.

A trigger spray container that prevents dry firing and solves the problem of interupted spray as the containers contents are dispensed and reduced to a level that allows the end of straw tip of trigger spray apparatus to become disengaged with liquid as the container is tilted towards the users target. As the user inverts or rotates the container from a vertical position, downwardly, towards a horizontal plain and aims the spray tip output nozzel towards the intended target, the liquid level adjusts within the container. Therefore, it becomes advantageous for end of straw tip to be positioned at the lowest point on container base, side of container base nearest target. This is achieved by forming an integral straw guide molded into the container body that provides a ramp for the straw to be guided on, thereby directing the straw tip to this position. The straw length of the trigger spray apparatus is of sufficient length such that it travels on ramp of integral straw guide and engages with intended base corner as trigger spray apparatus becomes securably attached to the mouth opening of container. The liquid contents of the container can now be fully consumed, without pumping air during operation, as the consumer uses the product in its entirety.

Apparatus and methods for root canal treatments are provided. In some embodiments, an aiming element may be used to position a high-velocity liquid jet near a desired location in the tooth. Embodiments of the aiming element may include an interrupter that deflects or impedes the liquid jet when it is not desirable for the jet to propagate from the aiming element. Embodiments of the aiming element may include an elongated member that permits passage of the liquid jet through a channel. The elongated member may include one or more openings, for example, on sides and / or ends of the member. Some root canal cleaning techniques include one or more applications of the liquid jet followed by application of a disinfectant such as, for example, an aqueous solution of sodium hypochlorite.

A corner shelf assembly for corner walls using a flat shelf member with two perpendicularly disposed edges. Each of the edges includes at least one tongue member that extends coplanarly and is removably inserted within respective casing members that are cooperatively mounted within openings at the corner walls. The casing members accepting the tongues from one of the edges are wider so that the flat shelf member can be slid horizontally after this first set of tongues is inserted. A latching mechanism is used to keep the flat shelf member in place. Alternatively, corner the shelf assembly may include locking clips that are inserted in the casings after the user inserts the tongues in the wider casings. The locking clips prevent lateral movements of the shelf assembly. The corner shelf assembly can be removed upon the application of a predetermined amount of lifting force to the shelf member.

A mask apparatus for a respiratory treatment can permit delivery of breathable gas to a user. In one example, the mask may employ a frame and cushion to form a seal for both mouth and nose. The frame may be adapted for coupling with a respiratory treatment apparatus so as to permit communication of a pressurized gas from the respiratory treatment apparatus. The cushion, which may be foam, may have a substantially under the nose configuration or over the nose configuration. The mask may have a common plenum chamber for both nose and mouth. The cushion may further define a centrally open lip superior region. The cushion may be adapted to couple with the frame directly or to the frame in conjunction with a cushion support clip. Various features of the cushion may further promote sealing and comfort for the under the nose design.

Surgical instrumentation and methods for performing a bypass procedure in a digestive system incorporate laparoscopic techniques to minimize surgical trauma to the patient. The instrumentation includes an outer guide member dimensioned for insertion and passage through an esophagus of a patient and defining an opening therein extending at least along a portion of the length of the outer guide member, an elongate anvil delivery member at least partially disposed within the opening of the outer guide member and being adapted for longitudinal movement within the outer guide member between an initial position and an actuated position and an anvil operatively engageable with the delivery member. The anvil includes an anvil rod defining a longitudinal axis and an anvil head connected to the anvil rod. The anvil head is at least partially disposed within the opening of the outer guide member when in the initial position of the delivery member and is fully exposed from the distal end of the outer guide member upon movement of the delivery member to the actuated position.

A ratchetable open-ended wrench having a slidable retractable jaw member in a slot in one of its jaws and having a cover plate, preferably two cover plates, welded to the jaw in a manner such that the cover plate forms a load-bearing structural member within the jaw.

A bottle assembly includes an inner vessel and an outer vessel. The outer vessel is adapted for holding a liquid, and has an open mouth through which the liquid is poured. The inner vessel is received within the open mouth of the outer vessel, and is adapted for storing contents separate from the liquid contained in the outer vessel. The bottom wall of the inner vessel is adapted for being ruptured when the inner vessel is positioned within the open mouth of the outer vessel, such that contents stored in the inner vessel can mix with the liquid contained in the outer vessel without removing the inner vessel from the outer vessel.

The invention is directed to a garment with an attached head-and-face cover, such as a ski mask, and a hood. The head-and-face cover has eye openings and a mouth opening. The garment has a body portion and a collar. When the head-and-face cover is not deployed on a head and face of the wearer, the head-and-face cover is inserted into a storage structure. The storage structure may be a pouch that dangles from the garment body portion by a connecting piece. In another embodiment, the storage structure may be a pocket sewn to the hood or to the front portion or back portion of the garment body portion.

An apparatus for communication between a site within a body and a source, depot, reservoir, device or machine external to the body via the mouth of the body, comprising an implant for placement in tooth-supporting bone, the implant having a first portion extending into the mouth external to the tooth-supporting bone, a second portion for being embedded in the tooth-supporting bone, and an opening extending along the implant from the first portion to the second portion. A sealing cap containing an antimicrobial substance may be provided to provide a seal when the apparatus is not in use. An external pump may infuse various medications or liquids, including those required by a person having a diabetic condition.

Systems and methods provide for automated, cyclic delivery and evacuation of a treatment or irrigation solution from a tooth root pulp chamber and pulp canals. A manifold has a base member sized and configured to rest on a crown of an instrumented tooth and a top member sized and configured to couple with the base member to define an inlet chamber and an outlet chamber. The distal end of a needle is passed through an opening between the inlet and outlet chambers and extended distally beyond the base member into a pulp canal. The proximal end of the needle includes an opening in fluid communication with the inlet chamber. A solution is transferred from a fluid supply source to the inlet chamber and through the needle into the pulp chamber and pulp canals. The spent solution is evacuated from the pulp chamber and pulp canals through the outlet chamber.

A plastic mouthpiece insert for allowing a wearer to whiten their teeth while getting a suntan, and have a generally oblong oval-rectangular opening with a curved rear end that abuts against the root surfaces of the frontal upper and lower teeth of the wearer. A raised front edge can protect the lips and separate in place about the opening to the mouthpiece. Whitening agents can be used to enhance the whitening effect so that ultraviolet light and heat source such as the sun or a sunlamp is all that it is needed. Reflective inner walls in the mouthpiece can magnify light to the teeth. The mouthpiece can include bite tables, and the side walls of the mouthpiece can be inwardly flared and funnel shaped for focusing and magnifying incoming light and heat. The mouthpiece can be colored to protect the inside of the wearer's mouth from receiving any light.

An aviation clamp device formed of a substantially rigid elongated jaw structure formed with an open throat portion formed between spaced apart and relatively angularly canted opposing drive and anvil plates and a backing plate and having an elongated mouth opening thereinto between the opposing drive and anvil plates and partially extending around peripheries thereof to the backing plate, the drive plate being formed with a pair of threaded apertures therethrough spaced adjacent to opposite ends thereof, and a ball-end coupler formed of a resiliently deformable part-spherical head projected from one of the drive and anvil plates on a substantially rigid reduced diameter stem relatively upstanding thereon; and a plurality of threaded thumb screws each structured for cooperating with one of the threaded apertures by threading therethrough from an external surface of the elongated jaw structure into the throat portion thereof.