Abstract: A tool set for implanting a rod in a human spine in conjunction with bone screws includes a pair of end guide tools that receive opposite ends of the rod in channels and under manipulation by a surgeon facilitate transport of the rod toward the bone screws attached to the guide tools. Each end guide tool includes a laterally extending, rigid, rod holding structure located near a bottom surface thereof. Intermediate guide tools having pass-through slots are utilized to guide the rod to the bone screws at intermediate locations. For bone screw implantation, the end guide tools and intermediate guide tools are assembled with a driver. The driver is coaxial with the respective guide tool and rotatingly mateable thereto. The driver includes a stem and a nut-type fastener, the stem receivable in the guide tool. The fastener allows for rotation of the bone screw without rotating the attached guide tool.

Abstract: A system, and method of using the system, for changing the angle of a bone of a subject is provided by the present disclosure.

Abstract: Disclosed is a fracture fixation plate assembly comprised of a body, a hinge, a pin, and one or more heads, in which the head or heads can pivot and displace laterally/medially and can tilt vertically with respect to the body of the plate, more efficiently and flexibly enabling the fastening of the body of the plate to a stable part of the bone prior to reduction of the fractured portion or portions of the bone.

Abstract: A pectus bar assembly including a bar support and a pectus bar. The bar support can include a fastener and a fabric. A fabric can encircle a first rib and a second rib of a human ribcage. The fabric can include a first free end securable to the fastener and a second free end securable to the fastener to tension the fabric around the first rib and the second rib. The pectus bar can include an elongate body. The elongate body can include an anterior side and a posterior side opposite the anterior side. The posterior side can be supported by the bar support between the first rib and the second rib.

Abstract: A pair of plate benders is provided for bending a bone plate having a plurality of screw holes and a plurality of tubular drill guides removably preassembled into the screw holes. Each plate bender has a first end, a second end, and a handle extending between the first and second ends. The first end has a lower table on which the plate is received, an upper retaining structure which is adapted to engage the tubular drill guides, a recess defined between the lower table and upper retaining structure into which a portion of the plate is received such that the plate extends over a portion of the table and below a portion of the retaining structure. The retaining structure engages the periphery of the tubular drill guides to secure the plate relative to the bending tool.

Abstract: The present invention includes devices, systems and methods for the storage, retrieval and placement of plates having wedges. A wedge plate tray includes an upper portion and at least one recessed portion, the recessed portion including a cavity sized to house the wedge and an additional cavity sized to accommodate placement and movement of an arm of an insertion instrument. The insertion instrument includes two arms connected at a hinge, a tip of each arm including a mating connector sized to engage a complementary mating connector on the wedge. In one embodiment of the method, the insertion instrument can be used to place the wedge plate in an osteotomy and where the wedge is a mobile wedge, a plate component can be adjusted to a desired position for securement while using the insertion instrument to hold the wedge in place in the osteotomy.

Abstract: Composite material screws and construction techniques are described comprising reinforcing fibers directed in different winding directions and/or angles at different layers (radial depths) of the screw. Optionally, the screw comprises composite material layers wound with fibers at both the pitch of the thread of the screw and at a steeper pitch (for example, about 45°). Optionally, an outer layer of the screw comprises a relative radiolucent construction and/or material, with a more radiopaque construction and/or material positioned underneath the outer layer such that at least a portion of the screw outline is delineated by a radioimaging technique (for example, fluoroscopy, CT, or MRI), while maintaining a sufficiently artifact-free image around the screw that the image characteristics of the surrounding tissue are still determinable.

Abstract: An endovascular near critical fluid based cryoablation catheter for creating an elongate lengthwise-continuous lesion in tissue comprises an elongate shaft, a flexible distal tissue treatment section, and a distal tip. A plurality of flexible tubes extend through the distal treatment section to transport a near critical fluid to and from the distal tip. The distal treatment section is controllably deployed to match the contour of an anatomical region to be treated. In embodiments the distal treatment section includes a superelastic material and can assume a plurality of different shapes based on the distance ejected from an outer sleeve member. When the catheter is activated, heat is transferred between a target tissue and the distal treatment section of the catheter thereby creating the elongate lengthwise-continuous lesion in the tissue.

Abstract: According to some embodiments, a method of treating a subject having diabetes or symptoms associated with diabetes is provided. The method includes delivering a neuromodulation catheter within a vessel (e.g., hepatic artery) having surrounding nerves that innervate the liver (e.g., sympathetic nerves of the hepatic plexus). The method may also include modulating (e.g., disrupting, ablating, stimulating) the nerves by mechanical compression, energy delivery, or fluid delivery.

Abstract: Systems and methods for endometrial ablation. The systems include a handle and elongated introducer sleeve extending to an expandable working end having a fluid-tight interior chamber. A thin dielectric wall surrounds at least a portion of the interior chamber and has an external surface for contacting endometrial tissue. The thin dielectric wall surrounds a collapsible-expandable frame and receives an electrically non-conductive gas. First and second polarity electrodes are exposed to the interior and exterior of the chamber, respectively. A radiofrequency power source operatively connects to the electrode arrangement to apply a radiofrequency voltage across the first and second electrodes, wherein the voltage is sufficient to initiate ionization of the neutral gas into a conductive plasma within the interior chamber, and to capacitively couple the current in the plasma across the thin dielectric wall to ablate endometrial tissue engaged by the external surface of the dielectric structure.

Abstract: A medical device that includes a support member, a heat insulator provided on at least a portion of a first surface of the support member, an energy output member configured to output energy, the energy output member provided on at least a portion of a first surface of the heat insulator, the output energy configured to treat biological tissue and a heat conductor provided on at least a portion of the first surface of the support member and contacting a second surface of the heat insulator, the second surface of the heat insulator opposite the first surface of the heat insulator, wherein a portion of the support member is located proximal than the energy output, and the energy output member is configured to transfer heat to the heat insulator, and wherein the heat conductor is configured to conduct the heat from the heat insulator to the support member.

Abstract: The electrosurgical systems and corresponding methods of the present disclosure involve an electrosurgical generator, sensing circuitry, and a controller. The electrosurgical generator includes a radio frequency (RF) output stage that supplies power to tissue. The sensing circuitry measures impedance of tissue. The controller controls the power supplied from the RF output stage to track a nonlinear power curve until the power supplied from the RF output stage has reached a predetermined peak power of the nonlinear power curve. The controller further determines whether a tissue reaction has occurred based on impedance measured by the sensing circuitry and controls the power supplied from the RF output stage during a cooling phase if the controller determines that a tissue reaction has occurred. The controller may further control the power supplied from the RF output stage to track a linear power curve.

Abstract: In the case of an instrument (10) for coagulation and fusion as well as for severing vessels, provision is made for two shanks (19, 20), between which a vessel is to be gripped and fused. A blade (21) for severing the coagulated and fused vessel is provided with an isolator (40), which isolates the blade (21) against at least one of the electrodes or shanks (19, 20), respectively. On the other hand, the blade (21) is preferably in mechanical contact with at least one of the electrodes or shanks (19, 20), respectively, so that a safe separation of the fused biological tissue or vessel, respectively, is attained. This concept can be used to increase the safety of surgery and to miniaturize the tool (18) towards smaller sizes.

Abstract: An improved surgical instrument having an end-effector capable of several different operations, including grasping, cutting, and sealing and/or coagulating tissue, and one of the operations is controlled by handle that is moveable relative to instrument to move end effector between two conditions. Providing a simplified latching mechanism for this moveable handle, which latching mechanism is formed of single integrally formed component arranged to engage with handle to allow end effector to be retained in one condition, thus leaving user's hand free to perform other functions of instrument. Therefore, a user may use surgical instrument to grasp tissue between end effector by activating end effector using handle, then use latch mechanism to latch handle in the end effector activation position, allowing surgeon to remove his hand from handle and perform some other task.

Abstract: A treatment instrument which is used under an environment filled with an electrically conductive liquid includes a probe, a hollow sheath and an insulating member. The probe has a distal portion to chip a treatment target part by ultrasonic vibration and which allows the distal portion to function as one pole in a bipolar electrode. The sheath surrounds the probe. The insulating member covers the sheath except for a partial region on the distal side of the sheath. The partial region on the distal side of the sheath functions as the other pole in the bipolar electrode.

Abstract: Systems, devices, and methods for electroporation ablation therapy are disclosed, with the device including a set of splines coupled to a catheter for medical ablation therapy. Each spline of the set of splines may include a set of electrodes formed on that spline. The set of splines may be configured for translation to transition between a first configuration and a second configuration.

Abstract: A cooling element includes a frame including one or more datums. The cooling element also includes a first window including a first proximal surface and a first distal surface. The first window is sealed to the frame. The cooling element further includes a second window sealed to the frame. The second window includes a second proximal surface and a second distal surface. The second window is configured to contact a target tissue or a tissue adjacent to the target tissue via the second distal surface. The cooing element also includes a coolant chamber located between the first distal surface of the first window and the second proximal surface of the second window and configured to receive a coolant. The first window, the second window and the coolant chamber are configured to receive and electromagnetic radiation (EMR), and transmit a portion of the received EMR to the target tissue.

Abstract: The invention provides a non-invasive skin treatment device (200) comprising: a light source (10) constructed for emitting treatment light (15), an optical system (20) constructed for focusing the treatment light along an optical axis (OA) to a focus position (320) inside the skin tissue (300), and an indenter (30) comprising a skin contact surface (34) having an aperture (A1) at a distance from the optical system for allowing the treatment light to be focused through the aperture into the skin tissue.

Abstract: Embodiments of a surgical laser systems may include a laser source configured to generate a laser energy; a laser fiber optically coupled to the laser source to discharge laser energy; a photodetector configured to generate an output signal indicative of an intensity level of electromagnetic energy feedback produced in response to the discharge of the laser energy; and a controller configured to control the laser source based on the output signal. Embodiments of a method of controlling a surgical laser system also are disclosed, wherein laser energy is generated using a laser source and discharged through a laser fiber. Electromagnetic energy feedback produced in response to discharging the laser energy is delivered to a photodetector. An output signal from the photodetector is analyzed using a controller. The laser source is controlled in response to analyzing an output signal using the controller.

Abstract: A laser therapeutic device for a laser endoscope capable of relatively reducing the diameter of the endoscope while being capable of emitting a laser beam of a uniform intensity over a wide area is provided. An optical guide element (a square-shaped rod lens 15, a guide tube 2b) having a quadrangular cross section and guiding a therapeutic laser beam emitted from the tip of an optical fiber toward the tip side of a probe is used. On the tip side of a probe tube 2 being a barrel, using clearances C1 to C4 formed between the optical guide element and the inner circumferential surface of the probe tube, a camera unit 11 as imaging means and white-color LED units 12 and an ultraviolet LED unit 13 as illumination means are arranged.

Abstract: This disclosure describes example adhesive medical patches that may be used in combination with one or more antimicrobial agents to create and/or maintain an area of human skin that is free from contaminants. According to some embodiments, the disclosure describes that the adhesive patches may contain an adhesive material affixed to the perimeter of an impermeable backing According to some embodiments, the adhesive patch may also have a permeable layer containing an antimicrobial agent located interior to the adhesive material on the impermeable backing.

Abstract: A system for estimating post-virtual stenting fractional flow reserve (FFR) capable of: receiving geometrical parameters of a blood vessel segment, the geometrical parameters comprising first, second and third geometrical parameters; with a proximal end as a reference point, deriving a reference lumen diameter function and calculating a pre-virtual stenting percent diameter stenosis based on the above geometrical parameters and the distance from position along the segment to the reference point; receiving a virtual stenting location; calculating a geometrical parameter of a virtual lumen of the post virtually-stented segment, deriving a post-virtual stenting geometrical parameter difference function and calculating a percent diameter stenosis based on the third geometrical parameter, the virtual stenting location and the reference lumen diameter function; taking derivative difference functions of the post-virtual stenting geometrical parameter difference function in multiple scales; and obtaining FFR based on

Abstract: In accordance with one or more embodiments herein, a system for optimizing a position of an implant having an individually customized implant hat and at least one implant protrusion extending from the implant hat in the direction of an implant axis in an anatomical joint of a patient is provided.

Abstract: Disclosed herein is a method of defining a mating surface in a first side of an arthroplasty jig. The mating surface is configured to matingly receive and contact a corresponding patient surface including at least one of a bone surface and a cartilage surface. The first side is oriented towards the patient surface when the mating surface matingly receives and contacts the patient surface. The method may include: a) identifying a contour line associated with the patient surface as represented in a medical image; b) evaluating via an algorithm the adequacy of the contour line for defining a portion of the mating surface associated with the contour line; c) modifying the contour line if the contour line is deemed inadequate; and d) employing the modified contour line to define the portion of the mating surface associated with the contour line.

Abstract: A detection and identification system of instruments for use with a surgical navigation system is described. The navigation system contains an instrument assembly containing a coil (of a receiver) having an interior space, an instrument configured to be removably coupled to the coil, and a prong affixed to the instrument and configured to be at least partially disposed within the interior space of the coil when the instrument is coupled to the coil, where the prong has a length corresponding to physical dimensions of the instrument. The navigation system can also contain a transmitter located within the body of a patient.

Abstract: A system and a method are disclosed that allow for generation of a model or reconstruction of a model of a subject based upon acquired image data. The image data can be acquired in a substantially mobile system that can be moved relative to a subject to allow for image acquisition from a plurality of orientations relative to the subject. The plurality of orientations can include a first and final orientation and a predetermined path along which an image data collector or detector can move to acquire an appropriate image data set to allow for the model of construction.

Abstract: A surgical implement selection process that is used in conjunction with a first surgical implement tray having a plurality of first surgical implements therein. A surgical implement selection system is provided that includes a display portion and an input portion. An image of the first surgical implement tray is displayed in a first display region of the display portion. The first surgical implements are displayed in a second display region of the display portion in an order that corresponds to the order in which the first surgical implements are used in a surgical procedure to define a surgical implement selection template. The surgical implements are provided to a person performing the surgical procedure in the order in which the first surgical implements are displayed in the surgical implement selection template.

Abstract: A computer-assisted medical device includes a first articulated arm, the first articulated arm having an end effector, a first joint set, a second joint set and a control unit. The control unit configures one or more joints in the first joint set to a floating mode, detects movement of the first joint set caused by a movement of the surgical table, drives the second joint set based on the movement of the surgical table, receives an instrument motion command to move the end effector while the surgical table is moving, and moves the end effector based on the instrument motion command. In some embodiments, the instrument motion command is relative to an imaging coordinate frame. In some embodiments, the imaging coordinate frame is based on a pose of an imaging device saved prior to the movement of the surgical table.

Abstract: Devices, systems, and methods for controlling manipulator movements include a manipulator arm coupled to a proximal base. The manipulator arm is configured to support an end effector and robotically move the end effector relative to the proximal base. The manipulator arm includes a plurality of joints between the end effector and the proximal base and a processor. The processor is configured to calculate joint movements of the plurality of joints that provide a desired position of the end effector using inverse kinematics of the manipulator arm and when a first set of one or more joints of the plurality of joints is at corresponding joint range of motion limits: determine a constraint based on a relationship between joint movement of the first set and a second set of one or more joints of the plurality of joints and apply the constraint within the inverse kinematics to provide haptic feedback.

Abstract: A method of constructing a system comprising one or more surgical arms, comprising: providing: a plurality of modular units, each modular unit comprising at least one surgical arm attached to at least one motor unit configured for actuating movement of the surgical arm; coupling one or more modular units to each other in an attachment configuration; displaying on a user interface one or both of an indication of the attachment configuration and a selection of an attachment configuration.

Abstract: An ultrasonic surgical system has an ultrasonic unit including an instrument operatively connected to an ultrasonic generator, wherein the instrument has an ultrasonic end effector on the distal end of a shaft. The system further includes a positioning unit including a movable arm adapted for releasably holding the instrument, whereby an operator may direct the positioning unit to position the end effector at a surgical site inside a body cavity of a patient for performing a plurality of surgical tasks. The system further includes a control unit operatively connected to the ultrasonic and positioning units, wherein the control unit is programmable with a surgical subroutine for performing the surgical tasks. The system further includes a user interface operatively connected to the control unit for initiating an operative cycle of the surgical subroutine such that the surgical tasks are automatically performed during the operative cycle.

Abstract: A surgical instrument includes: an adjustable end effector; an elongated instrument shaft defining an internal bore; and a drive assembly including a housing coupled to an end of the instrument shaft and an input device configured to facilitate controlled adjustment of the end effector via a drive cable extending along the bore of the instrument shaft. The input device includes: a drive shaft attached to a first portion of the drive cable, the drive shaft including an upstanding stem portion having a radially tapered outer surface; and a capstan attached to a second portion of the drive cable, the capstan defining an internal bore sized to receive the stem portion of the drive shaft, at least a lower portion of the internal bore having a radially tapered inner surface. The capstan and drive shaft are configured to transition from a disengaged state to an engaged state.

Abstract: User interface devices are disclosed. The device can include a body that can be held in a user's hand. The body has an outer surface that can be gripped by fingers of the user's hand to facilitate translation and rotation of the body by the user's hand. The device can include one or snore sensors disposed within the body. In some embodiments, the one or more sensor can provide one or both of position and orientation information of the body to a control system. The body can provide feedback to the user via the exterior surface of the body that is gripped by the user's fingers and/or can receive control inputs from the user via one or more of translation of the body, rotation of the body, pressing of the outer surface with the user's fingers, and changing of the angular orientation of the longitudinal axis of the body. Methods of using a user interface device are also provided.

Abstract: A container for disposal of medical waste is provided that comprises a receptacle with an open top. A lid is attached to the receptacle to cover the open top of the receptacle. The lid has an elongated opening sized to permit the introduction of medical waste into the receptacle. A closure flap is connected to the lid to selectively close the lid opening. The closure flap is movable between an open position, a closed position and a locked position. The closure flap is attached to the lid by axial hubs that extend from each side of the closure flap through openings in the side walls of the lid. Covers attached to the outside of the side wall of the lid and engaged with the closure flap axial hub. The container may also include a locking external cabinet that encloses the receptacle and can be mounted to a wall.

Abstract: A manual retraction tool for use with a surgical tool assembly of a surgical device includes a shaft, a rotation mechanism, and a trigger. The shaft is dimensioned to be inserted into a rotational connector of a surgical tool assembly and to effect rotation of the connector upon rotation of the shaft. The rotation mechanism configured to rotatably support the shaft. The trigger is operably connected to the rotation mechanism such that when the trigger is actuated from a first position to a second position, the rotation mechanism rotates the shaft about a longitudinal axis in a first direction to effect rotation of the rotational connector of the surgical tool assembly.

Abstract: A zero-suckback device for a disposable high-speed turbine dental drill handpiece includes two units respectively installed at two ends of the head of the handpiece. On one side of the handpiece head where a drill pin is installed, one unit consists of an elastic shaft sealing casing which is centrally embedded with a central framework made of hard substances and a non-elastic shaft sealing casing, and a lip portion of the elastic shaft sealing casing fits a wind wheel shaft with a tapered end. On the cover side of the handpiece head and between a button housing and a head housing, an O-shaped sealing ring is installed, and a one-way ball valve is installed at the center of the button housing. Suckback prevention measures are adopted at both sides of the handpiece head, so matters sucked back can be controlled to be a very low level, nearly zero.

Abstract: A device for to aid or help patients remove dental prostheses. The dental prosthesis removal tool preferably includes a small hook, which has a rubber cover. The hook is preferably attached to a bar and a handle, which could easily fit into a patient's hand. The tool is preferably made of a strong, rust free metal, e.g. stainless steel. The handle is preferably made of a hard, processed plastic, and is strongly secured to the bar. A kit of the components is also envisioned.

Abstract: Creating a digital tooth model of a patient's tooth using interproximal information is provided. Interproximal information is received that represents a space between adjacent physical teeth of the patient. A digital teeth model of a set of physical teeth of the patient that includes the adjacent physical teeth is received. One or more digital tooth models is created that more accurately depicts one or more of the physical teeth than the corresponding digital teeth included in the digital teeth model based on the interproximal information.

Abstract: An orthodontic device and methods thereof for correcting an arrangement of teeth are provided. The orthodontic device includes a plurality of brackets for attaching to teeth; a plurality of spring anchoring units, wherein each of the plurality of spring anchoring units is attached to one of the plurality of brackets; and a spring having a tension, two-dimensional longitudinal deformability and two-dimensional rotational deformability, wherein the spring is attached to each spring anchoring unit, wherein the tension is zero prior to attaching the plurality of brackets to the teeth, wherein further the tension is greater than zero immediately after attaching the plurality of brackets to the teeth, wherein further the tension is zero when the plurality of brackets is attached to the teeth and in an optimal position.

Abstract: The present invention discloses a passive self-ligating bracket, comprising a bracket body, wherein the middle part of the bracket body is sunken downwards to form an archwire slot; a locking piece in slide fit with the bracket body is arranged above the archwire slot; at least one locking position is provided on one of the bracket body and the locking piece; a fixing mechanism for fixing the locking piece at the locking position is arranged on one of the bracket body and the locking piece; the fixing mechanism comprises an elastic element located on one of the bracket body and the locking piece; the elastic element is provided with a bulge capable of being received at the locking position; when the locking piece is in a locked state, the bulge on the elastic element is received at the locking position; and when the locking piece is in an unlocked state, the end part of the bulge on the elastic element is in close abutment with one of the bracket body and the locking piece, and forces the elastic element to s

Abstract: A dental implant includes a body and a threaded surface. The body has an upper portion, a middle portion, and a lower portion. The upper portion of the body includes a generally cylindrical region. The lower portion of the body includes a generally inwardly tapered region. The middle portion of the body includes an outwardly extending bulge. A maximum outer diameter of the bulge is greater than (i) a maximum outer diameter of the upper portion and (ii) a maximum outer diameter of the lower portion. The threaded surface is on the body within at least the upper portion of the body, the bulge, and the lower portion of the body.

Abstract: The present invention relates to a detachable implant-coupling prosthesis, and more specifically to a detachable implant-coupling prosthesis which enables an implant and a coupling prosthesis to be easily coupled to each other and can be easily coupled to and separated from each other during revision and re-placement. According to the present invention, via the unique distinguishing structure capable of achieving easy coupling without using a screw fastening method screw fastening method, loosening and fracture do not occur, and an aesthetic effect and durability can be prevented from being degraded because it is not necessary to form a hole in a tooth. Furthermore, the coupling prosthesis can be easily separated without destructing a tooth when a problem occurs after the placement of an implant, and thus effects arise in that the inconvenience of a patient can be mitigated and cost can be reduced during the treatment of inflammation or periodontitis.

Abstract: A method of preparing organic and natural material for making teeth and typical dental devices or appliances having sufficiently hard and durable chewing surfaces, obtained from sustainable resources.

Abstract: The invention relates to a dental milling block (1) comprising a dental article (2) having an outer surface, the dental article having been produced based on personalized data, wherein the outer surface of the dental article is at least partially covered with a surrounding material. The invention further relates to a process of producing a dental milling block, the process comprising the steps of: ?a) providing a personalized Data Set C containing geometry data of the dental article and colour data related to said geometry data, ?b) generating a layer of hardenable material on a surface, ?c) applying a colour agent to the layer of hardenable material of step b), wherein the colour agent is applied to at least some regions of those areas of the layer of hardenable material which are related to the geometry data of the dental article, ?d) consolidating the result obtained in step c) thereby obtaining an at least partially hardened layer of material.

Abstract: The invention relates for producing permanent dentures without using any implants (screws) on the gum or using glue but using the vacuum of suction cells (suckers), between the natural gum and dentures, but using flexible thin plastic (approved by FDA) sheath between the gum and the dentures using suckers (similar to octopus) made on upper and lower surfaces of the sheath the upper sheath surface will have the same shape of the normal denture lower surface, similarly the lower sheath surface will have the same shape of the gum, the shape of the plastic sheath will always have the same shape of the gypsum modeled cast at the dentist clinic, for the gum surface, all the suckers will be (squeezed) pressed and create vacuum to hold the dentures to the gum and the dentures.

Abstract: A denture retaining system and a denture bar constructed to be affixed in a human mouth, the denture bar including a distal end, lingual-side surface, vestibular-side surface, bone-facing surface and superstructure-facing surface opposite the bone-facing surface. The bone-facing surface at the distal end is relieved from the superstructure-facing surface at the distal end by an angle of between 10° and 25° relative to an axis perpendicular to a longitudinal plane passing through the lingual side and vestibular side surfaces of the denture bar. The system also includes an overdenture superstructure having a distal surface that substantially conformingly mates to the denture bar distal end when the overdenture superstructure is positioned against the denture bar superstructure-facing surface, and is coupled to the denture bar by at least one attachment element located at a position to an anterior side of a first molar position.

Abstract: Apparatus and methods for endodontic treatment of teeth provide effective cleaning of organic material (such as pulp and diseased tissue) from the root canal system. In an embodiment, a compressor system generates high pressure liquid (e.g., water) that flows through an orifice to produce a high-velocity collimated jet of liquid. The high-velocity jet is directed toward a surface of a tooth, for example, an exposed dentinal surface, and impingement of the jet onto the surface generates an acoustic wave that propagates throughout the tooth. The acoustic wave effectively detaches organic material from dentinal surfaces and tubules. The detached organic material is flushed from the root canal system by the liquid jet and/or by additional irrigation.

Abstract: An oral care appliance in which a cleaning agent is injected from a supply tank and a method for use of such an appliance in oral care for the teeth of one or two arches using a mouthpiece is disclosed herein.

Abstract: An oral irrigator including a handle, a tip, and a pump at least partially received within the handle and fluidly coupled to the tip. The pump includes a pump body defining a pump chamber, an inlet valve regulating fluid flow into the pump chamber, an outlet valve regulating fluid flow out of the pump chamber, a piston, and a linkage operably coupled to the piston and a drive shaft of a motor. The linkage translates rotational movement of the drive shaft into movement of the piston in first and second directions within pump chamber. When the piston moves in the first direction, the inlet valve opens, allowing fluid to flow into the pump chamber, and the outlet valve closes. When the piston moves in the second direction, the inlet valve closes and the outlet valve opens, allowing fluid to flow out of the pump chamber.

Abstract: A electric toothbrush comprises a handle and a brush head. A motor is arranged in the handle and a transmission rod is arranged in the brush head. The motor has a rotating shaft, which extends from a casing of the motor. A transmission connection member is arranged between the transmission rod and the rotating shaft of the motor, one end of the transmission connection member is connected with the rotating shaft, the other end is connected with the transmission rod. A sealing member surrounding the rotating shaft is arranged at the rotating shaft extending position of the outer surface of the casing. The sealing member extends from the outer surface of the casing of the motor to the transmission connection member, and a gap between the inside of the sealing member and the rotating shaft constitutes a first cavity. A second cavity is formed between the sealing member and a sleeving cavity of the transmission connection member.