Abstract: A device for cleaning an instrument includes a manifold comprising one or more fluid inlets, and a tubular member rotatable relative to and extending distally from the manifold. The tubular member includes a proximal end, a distal end, and a fluid outlet at the distal end. The fluid outlet is configured to direct a flow of fluid generally across the distal end of the tubular member. The tubular member also includes one or more fluid passages fluidically coupled to the fluid outlet, and the one or more fluid passages extend from the fluid outlet to the manifold. The manifold and tubular member are configured to receive a shaft of an imaging instrument in a position such that the shaft of the imaging instrument extends through the manifold to the distal end of the tubular member. Systems and methods relate to instruments and cleaning devices.

Abstract: Embodiments of a system and method for endoscope cleaning and inspection are disclosed. In an example, an endoscope cleaning and inspection unit includes cleaning and testing capabilities operated via control equipment and a display screen, to operate leak testing equipment, flush control equipment, and optical inspection equipment for leak testing, flushing, rinsing, and inspection of an endoscope interior chamber (lumen) and exterior surfaces. In a further example, the endoscope cleaning and inspection unit may further operate and receive information from a borescope imaging device or a magnification imaging device, using an imaging sensor to capture images of an endoscope lumen or surface respectively, as captured or output on the display screen. Further embodiments provide for control, monitoring, data collection, data input, and data output with such imaging devices via the endoscope cleaning and inspection unit.

Abstract: The invention provides for a dental or surgical handpiece with an elongated handle sleeve (110) and a head piece (50) attached to the front end of the handle sleeve (110) that serves to to detachably receive a dental tool as well as for a clamping mechanism (20) formed in the head piece (50) to detachably hold the tool, the clamping mechanism (20) having a push-button (10) for actuating the clamping mechanism (20). The handpiece further has an RFID transponder (5) for identifying the handpiece. The push-button (10) consists of a heat-insulating electrically non-conductive plastic or m ceramic material with a plate-shaped recess that holds the RFID transponder (5). The push-button (10) has a flat round shape so that the RFID transponder (5), because of the equally flat round shape of its coil, can be integrated very well into it. Particularly advantageous ambient electrical conditions can be achieved for the RFID transponder as the push-button (10) is made of an electrically non-conductive material.

Abstract: A fluid-driven medical or dental handheld device includes a head, the head including a housing and a impeller rotatably mounted in the housing. The housing defines a receiving chamber for receiving the impeller, a main air inlet and an air outlet being defined in the housing and communicating with the receiving chamber. An inner surface of the housing surrounding the receiving chamber defines a plurality of grooves, the grooves being arranged at intervals along a circumferential direction of the housing. The grooves reflect rotating airflows directed to the grooves to change directions and speeds of the airflows to form interference airflows, which can effectively reduce the rotation speed of the head at idling, while ensuring the torque output of the head during grinding teeth.

Abstract: An in-vivo dental surgical guide verification method including: receiving first information including: dental surgical guide information of a dental surgical guide, and hard structure information of a hard structure of a patient's mouth; positioning the surgical guide within the patient's mouth; contacting a stylus to a surface of the hard structure of the patient mouth; acquiring image information corresponding to an image which includes at least a portion of the stylus and a portion of the dental surgical guide therein using an imager; and comparing the image information with the first information.

Abstract: The present invention relates to a dental guide system (100) for tooth preparation, comprising an electronic detection system (101) for detecting a three-dimensional actual tooth shape (103-I); a comparing device (105) for ascertaining spatial deviation regions (107), at which the ascertained actual tooth shape (103-I) deviates from a specified desired tooth shape (103-S); and data glasses (109) having a display device (111) for optically displaying the spatial deviation regions (107).

Abstract: The present invention relates to dental components used for guiding the insertion of a dental implant into a desired location in a patient's mouth using a surgical guide including a master tube. The present invention includes various components that can be used with the surgical guide and during a dental procedure using the surgical guide.

Abstract: A device and a method for making space between teeth that can efficiently form a necessary space between adjacent teeth in a short time and reduce the physical burden on both the patient and the person who gives treatment. The device for making space includes an ultrasonic oscillator, an ultrasonic vibrator which receives a driving signal from the ultrasonic oscillator and vibrates ultrasonically, a grinding tip to which the vibration from the ultrasonic vibrator is transmitted, and a power supply device which supplies power to the ultrasonic oscillator. The opposing surfaces of the adjacent teeth T are ground by ultrasonic vibration of the grinding tip inserted between the two adjacent teeth T.

Abstract: Methods and devices for interproximal dental restoration are disclosed. One version of the present disclosure provides a method for the restoration of a tooth including a top surface, and an interproximal surface facing an adjacent tooth. The method of restoration includes removing a portion of the top surface of the tooth, and a portion of the interproximal surface of the tooth to form a hollow cavity preparation extending from the top surface to the interproximal surface. The removed portion of the interproximal space is surrounded by a dental matrix. Restoration of the tooth further includes moving the dental matrix away from the hollow cavity preparation towards the adjacent tooth, and bonding at least a section of the dental matrix to the tooth. Light-curable composite resin is then injected into the cavity preparation and light cured.

Abstract: The invention relates to the application of a composition containing recombinant amelogenin and propylene glycol alginate (“PGA”) on to cut dentin tubules followed by installation of a definitive restorative in a single visit.

Abstract: The invention relates to the application of a composition containing recombinant amelogenin and propylene glycol alginate (“PGA”) on to cut dentin tubules followed by installation of a definitive restorative in a single visit.

Abstract: The invention relates to the application of a composition containing recombinant amelogenin and propylene glycol alginate (“PGA”) on to cut dentin tubules followed by installation of a definitive restorative in a single visit.

Abstract: The invention relates to a 3d-printed dental restoration precursor, a 3d-printed array comprising a 3d-printed dental restoration precursor, a kit of parts comprising at least two 3d-printed dental restoration precursors or 3d-printed dental restorations and a process of producing such a 3d-printed array, 3d-printed dental restoration precursor or 3d-printed dental restorations. The 3d-printed dental restoration precursor comprises at least one crown unit having an outer surface and an inner surface and at least one support element having a fixation section. The support element is connected through the fixation section to the outer surface of the crown unit in a particular region.

Abstract: A debonding tool for removal of orthodontic brackets includes a handle. An arm extends from the handle. The debonding tool includes first and second opposed fingers. A collar is translatable along the arm and operates to effect relative movement of the first and second opposed fingers between the open and closed positions.

Abstract: The invention is directed to a composition that safely removes a cured dental cement or resin from metal brackets, metal braces, and enamel surfaces of teeth. It contains eugenol, isoeugenol, methyl-eugenol or an isomer thereof. A method for removing orthodontic fixtures adhered with a dental cement or resin to the enamel surfaces of teeth from these surfaces by contacting the dental cement or resin with a composition containing eugenol.

Abstract: An orthodontic article is described comprising a cured composition comprising the reaction product of free-radically polymerizable resin comprising at least one monomer, oligomer and/or polymer, comprising at least two (meth)acryl moieties; a monofunctional reactive diluent; and a polymer or macromolecule comprising a free-radical photoinitiator group. The polymer or macromolecule has a molecular weight of at least 500 g/mole. In one embodiment, the cured composition comprises a first and second photoinitiator wherein at least one is a polymer or macromolecule. Also described are photopolymerizable compositions and methods.

Abstract: An orthodontic indirect bonding apparatus including integral custom bracket bonding pads and methods of making. The indirect bonding apparatus includes a receptacle having a frame at least partially surrounding the custom bracket bonding pad perimeter, the receptacle joined to the bracket bonding pad with a sprue and configured to receive a tooth. The custom bracket bonding pad is configured to complement contours of a portion of the tooth surface. The bracket bonding pad is formed integrally with the receptacle.

Abstract: The present disclosure provides methods, computing device readable medium, devices, and systems having a dental attachment placement structure. One dental attachment placement apparatus includes a body having an attachment placement surface that is to be placed on an attachment affixing surface of a tooth and wherein the attachment placement surface includes a portion that is shaped to allow placement of an attachment at a particular position on the affixing surface of the tooth and a portion of the body having a contour that is shaped to correspond with a contour of an alignment surface of a tooth and when the contour of the body and the corresponding contour is aligned, the attachment is located at the particular position and can be secured to the affixing surface of the tooth.

Abstract: A dental implant that facilitate insertion and can be used in all bone types. The implant includes a body having a coronal end, and an apical end opposite the coronal end. A tapered region may be adjacent the apical end. On the apical part one or more taps are provided so the tap is cutting when rotating, clockwise and counter-clockwise The implant can have at least one variable profile helical thread that extends along the tapered region. The implant can have also micro-threads below the main threads, a gradual compressing tapered core, a self drilling apical end and a narrow coronal region.

Abstract: A coupling element for dentistry applications having a tubular body which forms an internal duct that is open outward at respective ends of the body. A first end forms a first inlet for the insertion in the duct of the head of a pin which can be coupled directly or indirectly to a maxillary bone tissue. The first end has a recess provided along the edge of the first inlet and forms a guiding portion for the insertion of the head of the pin; along a segment of the duct which is contiguous to the first inlet there is a protrusion which is substantially aligned longitudinally with the recess, for contrasting the accidental rotation of a ring provided with a respective discontinuity, which can be arranged in the segment in order to lock the head of the pin.

Abstract: To improve the precision of a dental restoration, the present invention provides a dental restoration manufacturing method comprising: a first step of preparing a general-purpose wax bite which is formed of paraffin wax, and which is formed to be standardized in correspondence to a preset standard dental arch profile and is arranged between a part in which implantation is to be performed and an opposite corresponding part, and which comprises a variable matching part corresponding to the part in which implantation is to be performed and being softened when heated to the temperature greater than or equal to a preset temperature, and a press protrusion part that is formed integrally with the variable matching part and protrudes to correspond to the opposite corresponding part and that is softened when heated to the temperature greater than or equal to a preset temperature; a second step of respectively acquiring, through an image capture device, a plurality of scanning images of the part in which implantation i

Abstract: A custom tool for forming a dental restoration in a mouth of a patient includes a first mold body providing for a customized fit with at least one tooth of the patient. The first mold body includes a portion corresponding with at least a first surface of the tooth and an interproximal portion corresponding with an interproximal surface of the tooth, the interproximal portion being of unitary construction. The first mold body is configured to combine with the tooth of the patient to form a mold cavity encompassing a first portion of missing tooth structure of the tooth.

Abstract: The invention provides a dental prosthesis, comprising: an implant frame configured to be fixed into the mouth of a patient to support replacement of two or more teeth of the patient, the implant frame having an exterior surface, the exterior surface defining a first engagement profile; and an overlay adapted to be secured to the implant frame and to provide, or afford mounting of, the two or more teeth, the overlay having an internal cavity that extends along a substantial length of the overlay, the internal cavity defining a second engagement profile, wherein the second engagement profile is complementary to the first engagement profile, thereby allowing fitment of a substantial portion of the exterior surface of the implant frame within the internal cavity.

Abstract: A single-use oral delivery device includes a housing unit configured to house a predetermined amount of oral medication, vitamins and or minerals to be applied to an interdental space of a user, and an interdental device configured to be interlocked with the housing unit, wherein the interdental device includes a cap at a top portion for interlocking and sealing with the housing unit, and an applicator tip at a bottom portion for applying oral medication, vitamins or minerals to the interdental space.

Abstract: An interdental cleaner has a rod-shaped support which is made of plastics material and the rear end region of which has a handle part and the opposite front end region of which supports a coating made of a soft-elastic plastics material. At least one radially protruding finger which is integrally connected to the coating is arranged on the outside of the coating. A recess is formed in the outer surface of the coating, and the radially inner foot region of the finger is arranged in the recess and is connected to the coating at the bottom of the recess.

Abstract: Various systems, method, and compositions for treating a tooth are disclosed herein. For example, an apparatus for treating a tooth is disclosed. The apparatus can include a chamber having an access port which places the chamber in fluid communication with a treatment region of the tooth when the chamber is coupled to tooth. A fluid motion generator can be coupled to the chamber. The fluid motion generator can be configured to direct fluid across the access port to generate fluid motion in the chamber. In various embodiments, fluid motion (e.g., vortices, swirl, etc.) can be induced at or near treatment regions of the tooth, such as a root canal or carious region.

Abstract: A disposable smart electronic teeth cleaning device for cleaning a plurality of teeth is provided. The disposable smart electronic teeth cleaning device includes a liquid pump, a pipe and an U-shaped main body. The liquid pump provides a cleaning liquid. The pipe is in communication with the liquid pump. The U-shaped main body includes a teeth-containing groove and a liquid inlet. The teeth-containing groove contains the plurality of teeth. The liquid inlet is disposed at the teeth-containing groove and is in communication with the pipe. The cleaning liquid provided by the liquid pump flows into the teeth-containing groove via the pipe and the liquid inlet to clean the plurality of teeth in the teeth-containing groove.

Abstract: A dental suction assisting device includes an upper molar seat located at an upper portion of a body and having anti-separation protrusions and a space for allowing seating of upper molars, a lower molar seat located at a lower portion of the body and having anti-separation protrusions and a space for allowing seating of lower molars, a fastening portion having an insertion hole and a through-hole and allowing fastening of a suction tube, a suction port having a first suction hole and allowing secretions in an oral cavity to be sucked through the suction tube, a leg formed at each side of the lower molar seat, configured such that the respective legs are brought into intimate contact with opposite side surfaces of the lower molars and having partitions, and a wing extending from the leg, and seated between the lower molars and skin in the oral cavity.

Abstract: Provided are an electric handle, an electric toothbrush and an electric cleaning brush. The electric handle comprises a housing, a rear cover, a swing motor and a main control structure. By installing a vibration control mass with limited mass, the rotational inertia of the stator of the swing motor is increased, so that the vibration amplitude of the shell of the swing motor is reduced. It also reduces the vibration amplitude transmitted to the control circuit board, battery and electric handle, decreases the vibration feeling in user's hand, and makes the output shaft of the swing motor transmit effective swing output as much as possible. Then the swing output is transmitted to the toothbrush head or cleaning brush head installed on the output shaft. In this way, the cleaning effect and vibration reduction effect are better, the hand feeling is more comfortable, and the production cost is also reduced.

Abstract: A device for determining the relative positions of an upper and lower jaw has an upper carrier with an upper contact surface for the upper jaw and a lower carrier with a lower contact surface for the lower jaw, wherein the carriers in a position of use correspond to the device with an upper jaw and a lower jaw. In addition, the device has a system for detecting the relative spatial positions of the upper and lower carriers with respect to one another.

Abstract: An intraocular lens assembly is used in cataract surgery. An intraocular lens assembly (100) has a haptic (102) having a ring (106), a plurality of arcuate arms (108), and a plurality of haptic arm bases (110). Each of the arms (108) is connected with the ring (106) by a respective base (110). An optic (104) has at least two pairs of opposed holes (112). The holes (112) are positioned in the close proximity with an outer peripheral edge of the optic (104). The optic (104) is removably positionable in the haptic (102) by a snap fit lock forming the intraocular lens assembly. The intraocular lens assembly (100) has a first unlocked position wherein haptic (102) is dissembled from the optic (104), and a second locked position wherein the optic (104) is snap fitted in the haptic (102).

Abstract: The invention relates to an accommodating intraocular lens, having an optical axis (3), with the lens comprising at least two optical elements (1, 2), and haptics to allow mutual translation of said elements (1, 2) in a direction substantially perpendicular to the optical axis (3), in which at least two of the elements (1, 2) each comprising free-form optical surfaces. The invention also relates to a combination of such lens and an apparatus adapted for measuring the optical power of an eye.

Abstract: Intraocular lenses for reducing negative dysphotpsia (ND) are described herein. An example ophthalmic lens can include an optic (200) with a central optical zone (225) disposed about the optical axis (OA) and an attenuation optical zone (220) disposed about the central optical zone (225), wherein the attenuation optical zone (220) is contiguous with the central optical zone (225), and wherein optical power of the ophthalmic lens is gradually reduced within the attenuation optical zone (220).

Abstract: A method for deploying an expandable prosthetic heart valve in a patient includes introducing a guidewire into a patient and advancing the guidewire through a vasculature of a patient to a deployment site. A distal end portion of a delivery apparatus and the prosthetic heart valve mounted in a radially compressed configuration along the distal end portion are advanced over the guidewire. The prosthetic heart valve is positioned at the deployment site. A screw mechanism is rotated, which exerts an axially directed onto the prosthetic heart valve, causing the prosthetic heart valve to radially expand from the radially compressed configuration to a radially expanded configuration.

Abstract: The invention relates to an implant (1) for treating and/or for replacing a heart valve (100) diseased by an inflammation and/or infection, wherein the implant (1) has a catching device (2) which, in a compressed state, can be introduced in a minimally invasive manner into the body of the patient, and which can be expanded at the implantation site on the diseased heart valve (100), wherein the catching device (2) is designed, at least in the implanted and expanded state, to compartmentalise tissue changes or tissue deposits (101), in particular in the form of heart valve vegetation or deposits, in particular by using the catching device (2) to engage around and/or receive at least regions of the tissue change or deposit (101).

Abstract: This invention relates to the design and function of a compressible valve replacement prosthesis which can be deployed into a beating heart without extracorporeal circulation using a transcatheter delivery system. The design as discussed focuses on the deployment of a device via a minimally invasive fashion and by way of example considers a minimally invasive surgical procedure preferably utilizing the intercostal or subxyphoid space for valve introduction. In order to accomplish this, the valve is formed in such a manner that it can be compressed to fit within a delivery system and secondarily ejected from the delivery system into the annulus of a target valve such as a mitral valve or tricuspid valve.

Abstract: Embodiments of a radially collapsible and expandable prosthetic heart valve and method for crimping the prosthetic heart valve are disclosed. A method of radially compressing a prosthetic valve can include partially inserting the valve while in a radially expanded configuration into a crimping device comprising crimper jaws, wherein a portion of the valve comprising an outer skirt extends outside of the crimper jaws. The method can further include crimping the valve to a first partially collapsed configuration, further inserting the valve into the crimping device, such that the outer skirt is between the crimper jaws, and crimping the valve to a second partially collapsed configuration, wherein a diameter of the valve is smaller in the second partially collapsed configuration than in the first partially collapsed configuration.

Abstract: Guide wire apparatuses and methods. Guide wires may be utilized for guiding a delivery apparatus, for example a transcatheter mitral valve delivery apparatus to replace a native mitral valve. A guide wire may include a core body having a length, and an outer layer having a length and extending around the core body and along the length of the core body. A guide wire may include an intermediate layer positioned between the core body and the outer layer and configured to be retracted relative to the core body and the outer layer along the length of the core body and the length of the outer layer.

Abstract: The disclosure provides systems and related methods for delivering a prosthesis to a target location. The system includes a tether delivery catheter and a prosthesis delivery catheter, and also can include a lock delivery catheter or knot pusher, as desired. Various embodiments of useful valve prostheses are also disclosed.

Abstract: Mitral valve prolapse and mitral regurgitation can be treating by implanting in the mitral annulus a transvalvular intraannular band. The band is positioned so that it extends transversely across a coaptive edge formed by the closure of the mitral valve leaflets, to inhibit prolapse into the left atrium. At least one marginal chordae is severed, to permit leaflet closure against the band.

Abstract: A device for cardiac valve repair, the device comprising: a stent adapted to anchor to at least one tissue site, the tissue site located upstream with respect to a heart valve of a patient; and a neo-leaflet arranged to extend from the upstream anchoring means, the neo-leaflet comprising a free end, wherein the neo-leaflet is operable to extend across the heart valve via a commissure in between two heart valve leaflets of the patient's heart and locate the free end downstream from the heart valve and the neo-leaflet operable to coapt with the heart valve leaflets of the patient's heart to prevent and/or minimize a backflow of blood. The present invention is suitable for the treatment of heart valves using minimally invasive approaches. Additionally, the present invention is directed to a method of implanting a device for cardiac valve repair in a patient's heart.

Abstract: A valve cusp sizer includes a back surface brought into contact with a living body, and a hole that is formed on the top surface at a distance from the center in a left-right direction toward one side in the left-right direction and into which a support rod is inserted.

Abstract: An implant includes a component for fixed attachment to a bone. An underpass layer of a porous material is disposed on a first side of the component for fixed attachment. At least one strut is provided on the underpass layer. The at least one strut has a first surface contacting the underpass layer and a second surface opposite the first surface. The at least one strut comprises a non-porous material. An additional layer of the porous material fills a respective volume adjacent the at least one strut. The additional layer extends from a first side of the underpass layer to a predetermined height at or above the second surface of the at least one strut.

Abstract: A femoral orthopaedic prosthesis includes a metallic core extending from a proximal end to a distal tip. The metallic core includes a neck that is positioned at the proximal end and is configured to receive a prosthetic femoral ball. An elongated stem extends distally from the neck to the distal tip. The stem includes a proximal section extending distally from the neck, and a distal section that extends proximally from the distal tip. The elongated stem also includes a pair of spaced-apart beams that connect the proximal section to the distal section. An aperture is defined in the stem between the pair of spaced apart beams.

Abstract: A spacer for a knee replacement prosthesis. The spacer may include a lower surface, which has a locking component adapted to interlock with a tibial tray, an upper surface, the upper surface having a pair of condyle support platforms; and a frame positioned therebetween for anchoring the upper and lower surfaces thereto, the frame having a hollowed center defined by internal cavities. In some exemplary embodiments, the spacer may further include a fluid delivery system for localized antibiotic treatment to the surrounding joint. The delivery system may include a reservoir disposed within the internal cavity, a septum operatively connected to the reservoir, and fluid delivery element for dispensing a liquid medicament from the reservoir to the surrounding infection. The fluid delivery system may interact with external components to refill, communicate with, and control the system.

Abstract: A tibial tray for a resurfaced proximal portion of a tibia for a knee replacement for a patient includes, for example, a body having a superior portion, and an inferior tibia-engaging portion having a peripheral inferiorly-extending portion contactable with an underlying cortical bone and/or spaced apart from the underlying inner surface of the cortical of the tibia of the patient. In some embodiments in the total knee replacement, a greater portion of a shearing force acting transversely on the tibial tray and the resected portion of the proximal portion of the tibia of the patient is resisted by the at least one inferiorly-extending wall and the periphery of the resected proximal portion of the tibia compared to a portion of the shearing force being resisted along the center inferior surface of the tibial tray and the resected cancellous bone surface. Methods, robotic systems, and cutting guides are also disclosed.

Abstract: A tibial baseplate for tibial component of a knee prosthesis including: a bulk solid portion including a proximally facing surface adapted to accommodate a bearing element for the articulation of a femoral component of the knee prosthesis; a plurality of porous portions integral with the bulk solid portion having a porous portion contacting surface opposite to the proximally facing surface adapted to contact a proximal tibia. Advantageously, the plurality of porous portions are seamlessly incorporated and embedded in the bulk solid portion.

Abstract: Provided is a structurally stable interbody cage.

Abstract: A spacer separates bones of a joint using a driver tool having a threaded shaft. The spacer has a superior endplate with inferior facing ramps, and an inferior endplate with superior facing ramps. Two bearings are positioned between the endplates, each bearing has superior facing ramps which mate with the inferior facing ramps of the superior endplate, and inferior facing ramps which mate with the superior facing ramps of the inferior endplate. One bearing has a threaded aperture, and the other a thrust surface. A threaded shaft is threaded into the threaded aperture to push against the thrust surface to drive the bearings apart. As the bearings move apart, the mated ramps slide against each other to drive the superior and inferior endplates apart.

Abstract: A vertebral implant device is described comprising a wedge, a plate having an external surface configuration and one or more plate tine, a staple having one or more staple tine and a coupling device. The coupling devices is configured to couple the wedge, the plate and the staple whereby when the vertebral implant is secured in a vertebral body, the external surface configuration of the plate alters the relative orientation of a superior endplate surface plane and an inferior endplate surface plane of the vertebral body and alters the alignment of the spine. In some embodiments, plate tines and staple tine are configured to frictionally engage the vertebral body. In some embodiments, the coupling device is a screw and a nut. In some embodiments, interchangeable wedges are used to provide multiple implant device configurations.