Abstract: A cannula includes a funnel portion and a tubular portion extending distally from the funnel portion. The tubular portion defines a longitudinal axis. An inner lumen extending through the tubular portion permits a medical instrument to be advanced or retracted through the tubular portion. A first visual indicator on the tubular portion is indicative of a first defined remote center of motion about which the tubular portion is pivotable by a robotic system, and a second visual indicator on the tubular portion and spaced apart axially from the first visual indicator is indicative of a second defined remote center of motion about which the tubular portion is pivotable by a robotic system.

Abstract: A patient console for a robotic surgical system can include a base, a vertical lift attached to a top of the base and configured to provide up and down motion in a vertical axis, a yaw rotation device attached to the top of the vertical lift and configured to provide a yaw rotation about the vertical axis, a pitch rotation device attached to the top of the yaw rotation device and configured to provide a pitch rotation about a pitch axis orthogonal to the vertical axis, a translation device attached to the top of the pitch rotation device and configured to provide sliding translation along a translation axis, and a roll rotation device attached to the translation device to roll relative to the translation device about a roll axis to provide a roll to an instrument controller assembly. An angle of the translation axis and the roll axis relative to horizontal can be a function of the pitch rotation provided by the pitch rotation device.

Abstract: A tension compensation system for a robotically controlled medical device can include an instrument controller configured to operatively connect to a robotically controlled medical device to provide tension to one or more actuation cables of the robotically controlled medical device. The system can include an instrument control module configured to control the instrument controller to provide a compensation tension to at least one actuation cable of the one or more actuation cables to compensate for elongation of the at least one actuation cable of the one or more actuation cables based on actuation data associated with the at least one actuation cable of the one or more actuation cables.

Abstract: A teleoperated surgical system is provided that includes a surgical instrument that includes an end effector mounted for rotation about a slave pivot axis; a master control input includes a mount member, first and second master grip rotatably secured at the mount member for rotation about a master pivot axis; sensor to produce a sensor signal indicative of a slave grip counter-force about the slave pivot axis; one or more motors to impart a shear force to the mount member, perpendicular to the master pivot axis; one or more processors to convert the sensor signal to motor control signals to cause the motors to impart the feedback shear force to the first and second master grip members.

Abstract: A surgical guidance system for use with a robotic device configured to support and move a surgical tool includes a tracking system configured to track the surgical tool and at least one bone, a display device, and a control system coupled to the tracking system and the display device. The control system is configured to register a plurality of target trajectories to the at least one bone, determine a distance between the surgical tool and each target trajectory, automatically identify which one of the target trajectories is closest to and within a threshold distance of the surgical tool, and display, on the display device, the identified target trajectory relative to the at least one bone and a tracked pose of the surgical tool relative to the identified target trajectory.

Abstract: A surgical instrument wrap having at least one or a plurality of fibrous layers that cooperate with at least one agent or dye layer that is generally not visible until the at least one or plurality of fibrous layers is damaged or disrupted. The at least one diffusible agent or dye layer diffuses or wicks into the disrupted or damaged area. A fluorescent dye, a reactive dye, a conjugant dye or an absorption wavelength of approximately 200-400 nanometers in one embodiment and an emission wavelength in the visible spectrum so that when the surgical wrap is damage or disrupted and then exposed to, for example, a fluorescent or ultraviolet light source, the agent or dye fluoresces to provide an indication to the user that damage to the wrap has occurred. The user can presume that the items or instruments in the surgical tray may be contaminated.

Abstract: Methods of assembling a manifold for a medical waste collection system. A flapper valve unit is secured to a head of a cap. A filter element is positioned within a shell. Basket hands of the filter element are fitted between first pairs of ribs of the cap skirt. Fingers of the shell are fitted between second pairs of ribs of the cap skirt. The cap is secured to the shell to cover an open distal end of the shell. A drip stop is secured to the proximal end base of the shell to seat within the outlet opening. Ears may be fitted through holes defined by the flapper valve unit and cap holes defined by the cap so as to snap lock to the head of the cap. The hub of the flapper valve unit may be compressed with the ears snap locked to the head of the cap.

Abstract: An endorectal coil device holder is provided. The holder includes a base operable to be coupled to a surface, an arm extending form the base, and a receiver pivotably coupled with the arm. The receiver forms a receptacle operable to receive a coil base of the endorectal coil.

Abstract: A surgical instrument includes a body, an ultrasonic transducer assembly, and a transducer lock having a lock member configured to move between unlocked and locked positions. The transducer assembly is rotatably mounted along a longitudinal axis within the body such that the transducer assembly is configured to selectively rotate about the longitudinal axis. With the lock member in the unlocked position, the transducer assembly is configured to be selectively rotated about the longitudinal axis relative to the body. With the lock member in the locked position, the transducer lock is configured to seize the transducer assembly and inhibit rotation relative to the housing for coupling with an acoustic waveguide. The surgical instrument may also include an integral torque wrench for coupling the acoustic waveguide with a predetermined torque and an integral torque indictor for signaling to a user that the acoustic waveguide is coupled with the predetermined torque.

Abstract: The present invention relates to a protective nasal mask device which hermetically seals the nasal region of a user during an ENT procedure. The device facilitates access to the user's nose and throat using a plurality of surgical tools. The primary advantage of the present invention is to provide a nasal mask device which protects medical professionals from disease transmission during an ENT procedure. Additional advantages include a nasal mask device which enables usage of a plurality of surgical tools during an ENT procedure, a device which at the same time, prevents exposure of biohazardous waste to medical professionals. The device hermetically seals the nasal region of a patient during an ENT procedure.

Abstract: Systems and methods configured for simultaneous imaging and stimulation using a microscope system. The microscope system can have a relatively small size compared to an average microscope system. The microscope can comprise in part an imaging light source and a stimulation light source. Light from the imaging light source and the stimulation light source can be spectrally separated to reduce cross talk between the stimulation light and the imaging light.

Abstract: A surgical illumination system includes a light source having at least one laser diode configured to emit a light beam, the light beam having a focal point at a focal point plane, an optical fiber with a proximal portion configured to receive the light beam from the light source and a distal portion configured to emit the light beam from the light source, the proximal portion having an aperture opening. The size of the focal point is less than the size of the aperture opening.

Abstract: The present invention relates to a radiation therapy or microwave therapy or cryosurgery or ultrasound therapy reference positioning marker (5) adapted to be implanted in tissue using a hollow injection needle (4), wherein the marker comprises an elongated object with a longitudinal axis (CL) and have cross-sections (A-A, B-B, C-C, D-D, E-E, F-F) of the object, perpendicular to said longitudinal axis (CL), being adapted to fit within an inner diameter (DI) of the needle (4), wherein the marker (5) comprises a plurality of first segments (1) having a first cross-section and one or more second segments (2) having a second set of cross- sections, wherein an area of the first cross-section is selected relatively larger than area/s of the second set of cross-sections, and wherein the first segments (1) and second segments (2) are arranged alternately after each other along the longitudinal axis (CL), wherein the one or more of second segments (2) are provided with one or more deformation segments (22) adapted to e

Abstract: A lockable device, and methods for using said device, for inserting a marker into a patient's body. The device may be inserted into a patient's body in the locked state, transitioned into an unlocked state, and then used to deliver a marker to a precise location. The device may provide tactile and audible feedback once the marker has been placed and indicate that the device is ready for removal.

Abstract: Disclosed is a method for validating a decontamination procedure performed on a medical device using a decontamination system. The method comprises capturing a video stream of a work area in which the decontamination procedure is carried out by a user, analysing the video stream to identify one or more decontamination events in the video stream that correspond with the decontamination procedure being correctly performed on the medical device, the decontamination event or at least one of the decontamination events comprising applying a decontaminating composition of the decontamination system to the medical device using a wipe, determining, based on the or each identified decontamination event, if the decontamination procedure has been completed, and upon determining that the decontamination procedure has been completed, causing a corresponding indication to be provided to the user. The method may include alerting the user to potential errors and/or logging data to provide an audit trail.

Abstract: Disclosed herein are techniques related to safeguards against separation from portable medicine delivery devices. In some embodiments, the techniques may involve monitoring a wireless connection established between a portable computing device and a portable medicine delivery device. The techniques may also involve making a determination, based on the result of the monitoring, that the portable medicine delivery device is outside a predetermined range of the portable computing device. The techniques may further involve generating a notification based on the determination. The notification may be indicative of a user of the portable computing device being unaccompanied by the portable medicine delivery device.

Abstract: The present invention provides a working angle guiding device for dental implant and a method thereof. The working angle guiding device includes an intraoral securing device, a hand-held tool, a first triaxial attitude information sensor, a second triaxial attitude information sensor, and a controller. The working angle guiding method includes a preparing step, an installing step, a correcting step, a moving step, and a working angle adjusting step. The relative angle information of the first triaxial attitude information sensor and the second triaxial attitude information sensor is utilized to assist and guide the dentist to acquire the angle of implant drilling. The present invention has advantages in that the triaxial angle of the drill hole can be confirmed even after the patient dodges, tilts or moves his/her head, and that the first triaxial attitude information sensor can be flexibly mounted in the mouth or outside the mouth.

Abstract: A dental unit, which comprises connections for instruments and a control device and a microprocessor, which is arranged to control the dental unit. According to the invention, the microprocessor is arranged to control the dental unit according to a user specific user profile and the dental unit comprises a function for reading the user profile or a part of the user profile from an external record. The external record can be e.g. an USB memory stick or a record readable via a data network.

Abstract: Provided is a dental handpiece which can prevent degradation in visibility of a surgical field. The anti-reflection layer 100 is formed on the top surface and the side surface of the head portion 241 of the lid member 24 close to the root canal of the tooth, to which the operator pays attention, and further on the outer surface of the second cylindrical member 12 (refer to FIG. 3). Therefore, the reflection of light of a dental lighting tool provided with the anti-reflection layer 100 is suppressed, and degradation in visibility of a surgical field can be avoided. In addition, visibility of stains such as proteins adhering to the lid member 24 and the second cylindrical member 12 is improved, and cleaning thereof is facilitated.

Abstract: A drill guide assembly configured to engage a drill bit, including: a drill guide including: a drill guide tube including a ring and a flared end at a proximal end of the drill guide tube; a drill guide body with a central opening configured to receive the drill guide tube and a tube stop configured to engage the flared end; and a spring configured to engage the ring and distal end of the drill guide body; and a drill guide sleeve with a central opening configured to receive the drill guide including a ring stop configured to engage the ring and a sleeve distal end configured to engage a plate hole on a bone plate, wherein the spring is configured to bias the drill guide tube in a distal direction so that a distal end of the drill guide tube extends from the sleeve distal end.

Abstract: Endodontic instruments are used to clean and enlarge the endodontic cavity space (ECS), also known as the root canal system, of a human tooth. This document describes novel endodontic instruments that are radially compressible, and methods for their use. Some embodiments include a shank and a body with a working surface. At least a portion of the working surface may define a center of mass path that spirals. The center of mass of a transverse cross-section of the working surface at the shank end can be offset from the axis of rotation of the instrument.

Abstract: A protection device for transoral surgery includes: a main body configured to be fitted into an oral cavity of a human body and to expand a mouth vestibule between teeth and a lip of the human body; and at least one insertion device provided to the main body and having a through hole formed therethrough to enable insertion of a trocar required for a surgery. The main body includes: a tooth coupling part configured to be fitted on the teeth of the human body; an expansion part to be disposed on an outside of the tooth coupling part and configured to expand the mouth vestibule to allow the teeth and the lip to be spaced apart from each other; and an extension part configured to connect the tooth coupling part and the expansion part.

Abstract: Systems and methods are disclosed to prevent interference between two physical tooth models in a physical dental arch model by acquiring the coordinates of a plurality of points on the surfaces of each of the two physical tooth models and digitally representing the surfaces of each of the two physical tooth models by a mesh of points in three dimensions using the acquired coordinates. The meshes representing the surfaces of the two physical tooth models intersect at least at one point to form an overlapping portion. The method also includes calculating the depth of the overlapping portion between the two meshes to quantify the interference of the two physical tooth models.

Abstract: A dental appliance includes a first segment comprising a first plurality of tooth receiving cavities shaped to receive and to impart a first distalization force in a distal direction on a first part of a patient dentition on a first jaw. The dental appliance further includes a second segment comprising a second plurality of tooth receiving cavities shaped to receive and to impart a second distalization force in the distal direction on a second part of the patient dentition. The dental appliance further includes a connector shaped to span a plurality of anterior teeth of the patient dentition and to leave open a labial side of the plurality of anterior teeth. The connector operates to decrease transmission of one or more forces between the first segment and the second segment to limit transmission of at least one of the first distalization force or the second distalization force to the plurality of anterior teeth.

Abstract: An orthodontic device can include a bracket configured to support an orthodontic wire. The orthodontic device can include a locking assembly coupled to the bracket and switchable between a plurality of operational modes. The plurality of operational modes can comprise a first sliding mode in which the orthodontic wire is slidable relative to the bracket and a second locked mode in which the orthodontic wire is slidably locked relative to the bracket.

Abstract: A transfer part for removable attachment and handling of a dental implant, the transfer part including a body portion having a longitudinal axis and including a traversing hole along the longitudinal axis, a center portion arranged in the traversing hole of the body portion, and a fastening mechanism for reversibly securing the transfer part to the dental implant, wherein the center portion and the body portion are configured for a relative motion between each other to switch from a first position to a second position and vice versa, wherein in the first position, the fastening mechanism is in a released state to allow a removal of the transfer part from the dental implant, and in the second position, the fastening mechanism is in an engaged state to allow a securing of the transfer part to the dental implant.

Abstract: A dental bite block for final impression and bite registration includes at least one dental impression tray, a plurality of spikes, and at least one wax rim. The plurality of spikes is connected onto the at least one dental impression tray, and the plurality of spikes is oriented away from the at least one dental impression tray. Resultantly, the plurality of spikes is able to traverse into the at least one wax rim thus mounting the at least one wax rim onto the at least one dental impression tray.

Abstract: A method of scanning an oral cavity including: acquiring, using an intraoral scanner (IOS) head, without changing a position of the IOS head, a first image of a first region of interest (ROI) and a second image of a second ROI where the first and the second ROIs are of different portions of a dental arch of the oral cavity and do not overlap; reconstructing depth information for the first and the second ROI; and generating a single model of the dental arch by combing the depth information.

Abstract: Disclosed are a scanner system and a method for recording surface geometry and surface color of an object where both surface geometry information and surface color information for a block of the image sensor pixels at least partly from one 2D image recorded by the color image sensor. A particular application is within dentistry, particularly for intraoral scanning.

Abstract: An orthodontic wax dispenser is described herein. For example, certain embodiments of the present disclosure relate to a pocket-sized orthodontic wax dispenser that has an internal storage compartment for orthodontic wax, a press mechanism (e.g., a threaded piston) to compress the stored wax through an extrusion aperture, and optionally a lid or cover, which may double as a wax cutting mechanism.

Abstract: Systems, methods, and/or computer-readable media described herein provide technical solutions to the highly technical problems of machine generation of dental restorations. In particular, these systems, methods and/or computer readable media may provide technical solutions to aid in the creation of dental restorations that more closely resemble a natural tooth (including its internal optical structure). These systems, methods and/or computer readable media may help in virtually rendering a tooth, including its internal optical structure, and apply these renderings (e.g., digital models) to the fabrication of the dental restoration.

Abstract: In one aspect, the present application provides an anti-caries film, it contains a fluorine-containing silane, a film-forming agent, and an acidic substance.

Abstract: An evacuation dam apparatus including a frame having a top frame member, a bottom frame member, and two side frame members. A working area formed by the frame, a plurality of ports adjacent the working area, an outlet fluidly coupled with the plurality of ports. A fluid flow from at least a portion of the plurality of ports to the outlet forms a fluid flow path across the working area and at least a portion of the fluid flow path is formed within the frame.

Abstract: The present invention is directed to a controller (100) for generating a control signal for an oral care system (200), wherein the controller (100) is configured for receiving orientation data generated by the oral care system (200), wherein the orientation data describes at least one angle (102) between the oral care system (200) and a target tissue surface (300) in an oral cavity (400) or the angle relative to a reference vector, for instance the gravity vector, wherein the controller (100) is configured for comparing the received orientation data with at least one pre-defined orientation condition, and wherein the controller (100) is configured for generating a first control signal to trigger or adapt an oral care procedure performed by the oral care system (200) if the received orientation data fulfills the pre-defined orientation condition.

Abstract: A handle for an oral-care implement for safe and hygienic use by multiple users includes an electrical motor and a detachable head. The handle has a display for displaying instructions to control functional operation of the handle, a microcontroller for controlling the motor and the display, and at least one switch to allow a user to control the functional operation of the handle, including causing the output element to vibrate in at least one oral-hygiene mode having an oral-hygiene frequency and causing the output element to vibrate in a disinfection mode when the handle is being disinfected before or after being used for the oral-hygiene routine. The disinfection mode has a modulated frequency, different from the oral-hygiene frequency, and alternating up and down between a low modulated frequency and a high modulated frequency, wherein the high modulated frequency is at least 50 percent greater than the low modulated frequency.

Abstract: The device generally relates to a device for curing light hardening resin or resins, and more specifically, to a device for curing light hardening resins by exposure to selected light spectrum or spectrums for curing of light hardening resins through the incorporation of at least one light source which produces radiant light with the proper spectral frequency or frequencies to effect curing of light hardening resins used in combination with a gimbal wherein the resin or resins is placed.

Abstract: Interatrial shunts are described herein that are designed to benefit both the left side of the heart and the right side of the heart. The interatrial shunt is anchored in the atrial septum to permit blood to flow between atrial heart chambers across the atrial septum. In accordance with some aspects, the lumen of the shunt has an effective office area selected to permit blood flow across the atrial septum to unload the patient's left ventricle with beneficial effects on the patient's right ventricle. The shunts are structured to be suitably anchored at the atrial septum for long-term implantation. Further, the shunts preferably have insignificant late lumen loss. The interatrial shunts are expected to treat pathologies such as heart failure and pulmonary hypertension.

Abstract: An embolic protection device includes an expandable mesh net coupled to a catheter assembly used in an interventional procedure. The catheter assembly includes an outer catheter, an inner catheter, a compliant balloon, and the mesh net. The catheter assembly can be deployed in a lumen, such as an outflow graft of a left ventricular assist device, a blood vessel, or other bodily lumen. The mesh net is coupled to the inner catheter and is expanded by retracting the outer catheter when positioned in the lumen. The mesh net captures embolic debris before it is able to enter into the patient's blood stream.

Abstract: A stent is provided that includes a body extending between a distal and a proximal end. The body is defined by a plurality of elongated members, with each elongated member extending between a distal end that is coterminous with the distal end of the body and a proximal end that is coterminous with the proximal end of the body. Each of the plurality of elongated members are arranged so as to define a lumen extending along the length of the respective plurality of elongated members, the lumen extending between the distal and proximal ends of the body so as to form a lumen length. Each of the plurality of elongated members are configured to permit drainage of a fluid from within the lumen to an environment external the stent along the entire lumen length.

Abstract: There is provided a monitoring system for an organism including an analyzer apparatus and an implant, which is embedded under the skin of the organism, is connected to blood vessels under the skin, and forms a blood flow to an inspection port disposed above the epidermis, within the epidermis, or directly below the epidermis. The analyzer apparatus includes an irradiation apparatus that emits one or more lasers onto the inspection port of the implant embedded under the skin of the organism, and a detector that detects scattered light from the inspection port.

Abstract: Systems and methods of adjusting the diameter of an endoluminal prosthesis that allows for controlled radial deployment of the endoluminal prosthesis and the ability to revise the positioning of the endoluminal prosthesis after unsheathing. The endoluminal prosthesis includes a stent graft having a tubular graft wall, a stent, a main strand, a proximal strand, and a distal strand.

Abstract: An implantable soft tissue prosthesis device comprising a silicone elastomer-shell filled with silicone gel or liquid, which among the layers that constitute its shell includes a barrier layer formed of a low permeability silicone, which impedes the bleeding or diffusion of the silicone gel from the inside of the implant to its surroundings through the shell. This barrier layer is given a coloration different to the other layers of the shell, making it visible in the finished product. The coloration of the barrier layer gives the fabricator of the implant as well as to medical personnel, the possibility to identify the presence of the barrier layer and its homogeneity, improving the safety of the device.

Abstract: An intraocular lens implantation injector has a base body and an elongated actuation element projecting into a base body rear section and movably guided along an actuation axis. Actuation element movement is generated selectively by axial push actuation or by a screw actuation about the axis. The actuation element features an external thread at least on one section. At least one spring arm arranged at the base body has an inner surface thread engagement structure facing the external thread. A switch element, interacting with the spring arm, is rotatably or displaceably arranged on the base body. The switch element interacts with the spring arm via an operative contact. At least one switch element inner surface and/or spring arm outer surface involved in the operative contact is angularly inclined to the axis. Switch element rotation/displacement generates spring arm elastic deformation towards/away from the axis, thereby engaging/disengaging the thread engagement structure.

Abstract: Systems, methods, and devices for inserting an intraocular lens (IOL) into an eye may be provided. In an exemplary aspect, the present disclosure is directed to a haptic optic management system. The haptic management system may include a housing that includes a bore and a cavity disposed in a first surface of the housing. The cavity may include a first end portion, a second end portion, and a central portion, wherein the cavity provides access to the bore through the first surface of the housing. The haptic management system may include arms coupled to the housing. The haptic management system may include edge rollers coupled to the housing.

Abstract: A docking device for docking a prosthetic valve at a native valve of a heart includes a coiled body and a high friction sleeve. The coiled body has an upper region, a central region, and a lower region. The docking device is configured to be implanted at the native valve with the upper region positioned in a first chamber of the heart, the lower region positioned in a second chamber of the heart, and the central region positioned to extend around a plurality of leaflets of the native valve. A high friction sleeve covers at least a portion of the central region. The high friction sleeve comprises a material configured to generate more friction between the prosthetic valve and the docking device than an exterior surface of the coiled body.

Abstract: A system for replacing a native valve of the heart includes a delivery apparatus having a sheath and a prosthetic valve. The prosthetic valve includes a frame having an annular main body, a plurality of ventricular anchors attached to the main body, an atrial anchor attached to an atrial end portion of the main body, and a valve structure disposed within the main body of the frame. The prosthetic valve is disposed within a distal end portion of the sheath in a compressed, delivery state. When the prosthetic valve is deployed from the sheath, the main body of the frame radially expands to a radially expanded state, the ventricular anchors expand to a deployed state alongside the main body of the frame for capturing native leaflets of the native valve, and the atrial anchor expands to a deployed state extending radially outwardly from the main body.

Abstract: Systems and methods of atrioventricular valve replacement are provided. In various embodiments, an arch-like support structure is provided that is insertable and implantable into a heart and is positioned in the mitral annulus to replace a native mitral valve. The support structure is operable to support, and various systems comprise leaflet and chord structures operable to control and regular blood flow between chambers of the heart.

Abstract: A prosthetic device, such as a prosthetic heart valve, can include a frame that is radially expandable and compressible between a radially compressed state and a radially expanded state. In some examples, the prosthetic device can include locking mechanisms that are configured to hold the prosthetic device in a radially expanded state. In some examples, the locking mechanisms can be integrated into the frame of the prosthetic device.

Abstract: A prosthetic heart valve configured to replace a native heart valve and having a support frame configured to be reshaped into an expanded form in order to receive and/or support an expandable prosthetic heart valve therein is disclosed, together with methods of using same. The prosthetic heart valve may be configured to have a generally rigid and/or expansion-resistant configuration when initially implanted to replace a native valve (or other prosthetic heart valve), but to assume a generally expanded form when subjected to an outward force such as that provided by a dilation balloon or other mechanical expander. An inflow stent frame is expandable for anchoring the valve in place, and may have an outflow end that is collapsible to a limited degree for delivery and expandable post-implant to facilitate a valve-in-valve (ViV) procedure. The hybrid heart valves eliminate earlier structural bands, which both reduces manufacturing time and facilitates a ViV procedure.

Abstract: A guide wire introduction device for positioning at least one guide wire around a heart valve. The device includes a first catheter provided with a distal deflection system, a second catheter inserted inside the first catheter, at least one lumen capable of causing a guide wire to slide therein and provided with a distal deflection system for deflecting the end thereof through an angle greater than 90°, and a third catheter inserted inside the first catheter. The third catheter has a guide wire capturing device therein and is provided with a distal deflection system.