Abstract: An expandable and foldable mayo stand has a support column having first and second ends and a longitudinal axis. A table top is connected to the first end of the support column, and a base is connected to the second end of the support column. The table top is formed in two halves having a hinge connection extending along a hinge axis perpendicular to the longitudinal axis, whereby the table top halves can be pivoted between an open position in which they are coplanar and a collapsed position in which they are substantially parallel. The base has a central portion with wings hinged thereto; each wing has a plurality of legs connected to it by respective pin connections, so that the legs can be folded from a deployed configuration to a compact storage configuration.

Abstract: A device includes a support body with a substantially “C” squared-shape. The support body includes a support member and upright elements arranged on opposite sides of the support member that extend substantially orthogonally from the support member toward a surgical table. The device further includes one or more adjustment mechanisms connected to respective upright elements that adjust the spacing of the support member with respect to the surgical table to accommodate a patient's body positioned on the surgical table.

Abstract: A surgical drape is provided that has a drape body that has an upper surface and an oppositely disposed lower surface. A sleeve extends from the drape body into which an arm of a patient is located when the drape is positioned on the patient. A sleeve attachment component is located on the sleeve, and a body attachment component that is located on the drape body. The sleeve attachment component is attachable to the body attachment component in order to attach the sleeve to the drape body at a first location. A fenestration is present through which a portion of the patient can be accessed when the drape is positioned on the patient.

Abstract: A surgical drape is provided that has a drape body that has an upper surface and an oppositely disposed lower surface. The drape body has a forward edge and an oppositely disposed rearward edge. The drape body has a centerline that extends from the forward edge to the rearward edge. A guardrail is located at the upper surface of the drape body.

Abstract: Systems, methods, and devices are provided for assisting or performing guided interventional procedures using custom templates. The system uses pre-procedure scans of a patient's anatomy to identify targets and critical structures. A template is then manufactured containing guide elements. During a procedure, the template may be aligned to the patient and instruments passed though the guide elements and into various targets. The template may be aligned using one or more of, for example, a position sensing system or a live imaging modality to register the patient to the template. The system makes optional use of devices designed to immobilize or track an organ during therapy.

Abstract: A system and method for coordinated and controlled abdominal gas insufflation includes clamp configured to engage an abdominal wall. A needle advancement control is configured to receive a needle and advance the needle toward the clamp to extend into a portion of the abdomen. A feedback device is configured to monitor the needle as it is advanced into the portion of the abdomen of the subject and provide feedback indicating that the needle has pierced the portion the abdomen.

Abstract: The invention relates to a module for driving a robotic catheterisation system, comprising a base and mobile equipment that rotates in relation to the base about a rotational axis, and comprising a support receiving a flexible medical body; a device for driving in translation, suitable for generating a translation of said body in the main direction; a regulating device comprising a push element which is mobile in relation to the receiving space in a lateral adjustment direction perpendicular to the main direction; and a system for transferring motive energy comprising a control part carried by the base and a transmission part carried by the mobile equipment, the motive energy transfer system being suitable for moving the push element irrespective of the relative orientation of the mobile unit and the base.

Abstract: The invention concerns a module for guiding an elongate medical part along an elongation axis for a robotic system comprising: mobile apparatus mounted so as to rotate relative to a base about a rotational axis, and defining a space for receiving the elongate medical part, and comprising a rotational guiding system comprising a passage region for the elongate medical part corresponding to the location of the passage of the elongate medical part through the mobile apparatus, and a plurality of rotary guiding portions distributed about the rotational axis, an access aperture comprising an angular aperture of at least 30°.

Abstract: A system and method for movement control includes a controller coupled to a computer-assisted surgical device having a first movable arm coupled to a manipulatable device having a working end and a second movable arm coupled to an image capturing device. The controller is configured to receive first configurations for the first movable arm; receive second configurations for the second movable arm; receive a plurality of images of the working end from the image capturing device; determine a position and an orientation of the working end; determine a first movable arm position and trajectory for the first movable arm; determine a second movable arm position and trajectory for the second movable arm; determine whether motion of the movable arms will result in an undesirable relationship between the movable arms; and send a movement command to the first or second movable arm to avoid the undesirable relationship.

Abstract: A method for monitoring a reprocessing device for endoscopes the method including: logging one or more process parameters as well as a time of each reprocessing operation over a plurality of reprocessing operations for at least one endoscope in at least one reprocessing device; storing the logged one or more process parameters in association with the respective reprocessing operation, and performing a trend analysis of at least one logged process parameter in an evaluation device via the one or more logged process parameters.

Abstract: A surgical instrument includes an outer housing shell defining a cavity. The outer housing shell defines an upper outer housing half and a lower outer housing half. The upper outer housing half defines a longitudinal axis. An instrument module is selectively insertable into the cavity of the outer housing shell. The instrument module includes an inner housing shell, at least one motor disposed within the inner housing shell, a control board being in electrical communication with the at least one motor, and an energy source being in electrical communication with the at least one motor and the control board.

Abstract: A medical device adapted to be positioned in relation to an incision made in the skin of the patient is provided. The medical device comprises a vacuum sealing device comprising an internal vacuum sealing member adapted to be positioned inside the body of the patient, for creating a vacuum seal between the medical device and human tissue inside of the skin of the patient. By providing vacuum sealing inside of the body of the patient the surface of the skin can be kept unaffected, which means that no hematomas or discoloring of the skin will occur, also the internal vacuum sealing member makes it possible to seal further inside the body of the patient and thereby isolate certain areas in the body of the patient.

Abstract: A puncture planning apparatus has: a simulation unit that simulates movement of an organ and a puncture needle by simulation using an organ model; and a planning unit that plans, based on the simulation result, how to move the puncture needle when an actual organ is punctured. The simulation unit executes a plurality of times of the simulation of an operation to advance the puncture needle while correcting an angle of the puncture needle so as to follow the movement of the target segment due to deformation of the organ, conditions of an advancement speed of the puncture needle are changed for each of the plurality times of the simulation, and the planning unit performs planning using the best simulation result out of the plurality of simulation results acquired under different conditions of the advancement speed.

Abstract: A method includes receiving image data, receiving surgical procedure data, and generating an operation plan. The image data is associated with anatomical structures in a nasal cavity of a patient. The image data and the surgical procedure data are received through a computing system. The act of generating an operation plan includes identifying a path for a surgical instrument in accordance with the image data and in accordance with the surgical procedure data. The act of generating the operation plan is performed through a computing system. The act of generating an operation plan further includes generating one or more instructional images depicting the identified path for the surgical instrument in a depiction of anatomical structures in the nasal cavity of the patient.

Abstract: Devices, systems, and methods configured to assess the severity of a blockage in a vessel and, in particular, a stenosis in a blood vessel, provide visual depictions of vessel that allow assessment of the vessel and, in particular, any stenosis or lesion of the vessel, simulate one or more treatment options for the vessel, and perform treatment on any stenosis or lesion of the vessel, including guiding placement of one or more treatment devices are provided. The method can include obtaining pressure measurements from first and second instruments positioned within a vessel of a patient during a diagnostic procedure where the second instrument is moved longitudinally through the vessel; identifying a treatment option based on the obtained pressure measurements; and performing the identified treatment option, wherein a user display guides placement of one or more treatment devices associated with the identified treatment option.

Abstract: A surgery assistance apparatus includes an organ region extraction unit that extracts a tubular-organ region from a three-dimensional image obtained by imaging a tubular-organ and a blood vessel dominating the tubular-organ, a blood vessel region extraction unit that extracts a blood vessel region dominating the tubular-organ from the three-dimensional image, a branching structure extraction unit that extracts a branching structure of the blood vessel from the extracted blood vessel region, and a dominated region identification unit that identifies, with respect to an arbitrary partial blood vessel corresponding to an upper edge branching at least once to reach an edge including a terminal-end of the extracted branching structure, a dominated region in the tubular-organ region that is dominated by the arbitrary partial blood vessel by using positional relationships between a plurality of terminal end points present after the edge of the arbitrary partial blood vessel branches last and the tubular-organ region

Abstract: Systems and methods for creating a treatment plan for cosmetic procedures, for example, a hair transplantation procedure, are provided. The treatment plan allows user to provide input on a proposed hair element using a free-hand drawing in a two-dimensional plane, and for the proposed hair element to be generated and displayed on a three-dimensional model of a body surface. Various techniques and methods described in the application provide for improved planning of a natural looking hair.

Abstract: A computer-assisted surgery system includes a display, an input device configured to receive data input by a user, and a processor, coupled to the input device and the display. The processor is configured to establish a first position of a pre-operative center of rotation of a joint in a first coordinate space of a first bone and a second coordinate space of a second bone and establish a second position of the pre-operative center of rotation of the joint in the first coordinate space, wherein the second position is a projection into the first coordinate space of the position of the pre-operative center of rotation maintained in a constant position in the second coordinate space. The processor is further configured to determine a change in a parameter associated with the joint based on the first and second positions and output a result indicating the determined change to the display.

Abstract: An illumination system for adjustably positioning an illuminator in a surgical field in a patient includes an anchor element and an illumination element. The anchor element is configured to be releasably coupled with the patient, and the illumination element is coupled to the anchor element. The anchor element or the illumination element is configured to be coupled, uncoupled, and recoupled with the patient or adjacent surgical equipment. This allows repositioning of the illumination element at a plurality of positions in the surgical field without interfering with adjacent surgical instruments, and further permits adjustment of illumination in the surgical field.

Abstract: A shape sensing system includes a guide tube (304) and an optical shape sensing device (104) including one or more optical fibers and being proximally fixed at a fixation point and being disposed within the guide tube. An interventional instrument (102) is rigidly attached to a handle (212) to prevent rotation of the instrument relative to the handle. The instrument has a lumen configured to receive the guide tube therein such that the optical shape sensing device is unconstrained throughout the instrument and the handle, and the guide tube is free to slip relative to at least rotation of the instrument and the handle without transferring torsional friction to optical shape sensing device.

Abstract: A puncture needle guiding device is disclosed, which can include a casing; an ultrasound transmission-reception unit which is disposed inside the casing and which transmits and receives ultrasound; and a guide groove which is provided in the casing and which guides a curved puncture needle adapted to puncture a subject body.

Abstract: The present invention refers to a portable device for identification of surgical items with magnetic markers, method for identifying surgical objects with magnetic markers and system for the prevention of retention of surgical items with magnetic markers. The present invention can be used in surgical centers, with the aim of detecting surgical elements/objects (5) retained in the patient after surgery. The present invention aims to provide instrumental support in object location surgical (5) retained inside the body cavities for detecting artifacts forgotten after a surgical procedure, by means of device and specific objects and method and system for their identification.

Abstract: Medical instruments, particularly, endodontic instruments with unique limited memory characteristics, and methods for making such instruments. One embodiment includes heat treating an endodontic blank prior to forming a working portion of the endodontic instrument.

Abstract: A partial dental prosthesis (1) having at least one surface (2) for forming a chewing surface of a posterior tooth (3), wherein the partial dental prosthesis (1) includes a composite material (4) and the composite material (4) contains at least one organic binding agent (5), preferably methacrylate, and, preferably inorganic solid particles (6) as filler, wherein at least the surface (2) for forming the chewing surface, preferably the entire outwardly facing surface, of the partial dental prosthesis (1), is formed at least in some regions, preferably completely, by a layer (7) that includes fused-together solids particles (6).

Abstract: Cheek and lip expansion devices including an upper frame portion configured to extend about an upper dental arch, and a lower frame portion configured to extend about a lower dental arch. The upper and lower frame portions may each include first and second side members, each with anterior and posterior regions. An upper connecting member may extend between the anterior regions of the upper side members. A lower connecting member may extend between the anterior regions of the lower side members. The posterior regions of the upper and lower side members on respective sides of the frame are joined to one another to form a bendable radius that resists bending at a distinct point. The bendable radius on opposed sides permits the frame to be collapsed top to bottom. The frame may be collapsible side-to-side. A posterior crossbar may be provided extending between the posterior regions of the side members.

Abstract: Method and system for establishing an initial position of a tooth, determining a target position of the tooth in a treatment plan, calculating a movement vector associated with the tooth movement from the initial position to the target position, determining a plurality of components corresponding to the movement vector, and determining a corresponding one or more positions of a respective one or more attachment devices relative to a surface plane of the tooth such that the one or more attachment devices engages with a dental appliance are provided.

Abstract: The present invention relates to systems and methods for detecting deviations from an orthodontic treatment plan. One method includes receiving a tracking model, performing a matching step between individual teeth in a plan model and the tracking model, comparing the tracking model with the plan model, and detecting one or more positional differences.

Abstract: The present disclosure includes method, system, apparatus, and indicator embodiments. One apparatus includes an appliance for placement over one or more teeth and a release agent receptacle including an outer portion provided on appliance surface, an inner portion provided within the outer portion, and one or more apertures formed in the outer portion.

Abstract: Orthodontic expander comprising a left frame (T1) and a right frame (T2), wherein said left frame (T1) and right frame (T2) respectively comprise a left body (1) and a right body (2) provided with means for their anchorage to the teeth of a dental arch, wherein said bodies (1.2) have through holes (10) oriented in an expansion direction (d), wherein said frames (T1, T2) are slidingly mounted along said expansion direction (d) by means of guides (4) inserted in said holes (10) of said bodies (1.2), wherein the distance (h) between the said bodies (1, 2) is adjusted by means of a screw (5) screwed into the body (2) of one of said frames, wherein said screw (5) has an operating head (51) positioned between said bodies (1.2), and wherein elastic means (M) are positioned and acting between said frames (T1, T2) and can be activated or reactivated by acting on said screw (5) which compresses them to activate or reactivate them when desired.

Abstract: An orthodontic bracket is disclosed having three archwire retention channels in the mesial-distal directions, a central channel and two side channels. The two side channels each include a pair of spaced apart inverted archwire retaining regions having a recess that opens generally towards the bracket base. Each such recess is for grasping or holding an archwire therein. Each of the side channels has an archwire retaining ridge extending gingivally-occlusally along the adjacent side of the bracket base between the two retaining regions of the channel. For each channel, its retaining ridge exerts a force on a portion of an archwire facing away from the archwire portion residing in the recesses of the retaining regions of the channel. The force on the archwire is directed toward the interiors of the recesses of the retaining regions for assisting in seating the archwire in the recesses.

Abstract: The invention relates to an implant for osseointegration into a jaw bone, comprising a receiving opening one section of which is designed as an inner polygon, and said implant comprising an indexation at its distal end that reproduces the geometry of the inner polygon.

Abstract: A cradle, assembly, system and method for installing a prosthesis at a surgical site. The cradle temporarily engages the prosthesis and holds it in the correct orientation and position adjacent the surgical site. An aperture is defined in the cradle and a portion of the prosthesis is received therein. In one embodiment, the cradle, assembly and system are used to install a final dental prosthesis in a patient's mouth in a single visit to the dentist's office. A securement member pins the surgical template and subsequently the cradle to the jaw. A sub-structure on the final dental prosthesis is received in the aperture in the cradle. Cylinders attached to implants anchored in the jaw extend through holes in the sub-structure and are bonded to the prosthesis. The cradle is detached from the jaw and from the prosthesis prior to screws being re-inserted through the cylinders and into the implants.

Abstract: A dental implant has a body and a plurality of distinct roots that extend outwardly from the main portion that generally define a coronal-apical axis. A porous tantalum metal portion is disposed at the body for engaging bone and the plurality of distinct roots are configured to resist a torsional force that is applied to the dental implant and around the coronal-apical axis.

Abstract: A dental prosthesis includes an implanting end, a coupling end, and a screw portion between the implanting end and the coupling end. The dental prosthesis further includes a positioning marker portion located adjacent to the coupling end of the dental prosthesis. The dental prosthesis can be precisely located in an alveolar bone of a patient. A dental implant includes the dental prosthesis and an abutment. The abutment includes a prosthesis coupling end. The prosthesis coupling end of the abutment is coupled to the coupling end of the dental prosthesis.

Abstract: The invention relates to a dental abutment with internal connection to an implant and fixing by means of a fixing screw. The abutment is provided, apically at the connection end thereof with anti-rotation means for positioning and fixing the orientation of the abutment with respect to the implant, and with a through hole configured for the passage therethrough of the fixing screw, the axis of which extends in the longitudinal direction to the apical connection end. The anti-rotation means comprise a plurality of longitudinal protrusions separated from each other which extend in the direction parallel to the axis of the through hole at the apical connection end, the protrusions being equidistant with respect to said axis and being configured as merlons such that the separation space between two adjacent protrusions is connected to the through hole.

Abstract: A dental abutment, or a dental implant having an integrated abutment, in which the occlusal part of the abutment to which the dental prosthesis is to be cemented features a shoulder having a reverse margin. At the point where the shoulder meets the outer profile of the gingival part of the abutment, the shoulder is at an acute angle with respect to the longitudinal center axis of the abutment, thereby causing any cement ejected during mounting of the prosthesis to be ejected in a direction away from the gingiva.

Abstract: A full mouth reconstruction method and apparatus includes a denture molding structure mounted onto a patient's maxilla and mandible after being filled with an impression material, so that a static molding of the patient's gum can be performed based on the patient's occlusion. Important reference data including the vertical height of occlusion, facial midline, horizontal occlusion line, connecting line between two pupils and nose-ear horizontal line are recorded for facial and oral reconstructions while the patient is biting a first recording device, and the facial movements of the patient's chewing and speaking are recorded quickly while the patient is biting a second recording device. Records of a metal calibration are applied to obtain data of a patient's front-and-rear, left-and-right, and up-and-down maxillary and mandibular movements through facial movements of a patient's chewing and speaking, and these data are provided to a dental mold technician for producing the denture.

Abstract: Bite fork for check-bite, especially with position marker elements for position determination in a position determination system, wherein the bite fork comprises recesses at the contact surface for partial visualization of the tooth surface to an image sensor placed into the mouth cavity of a patient and markers, which are detectable by said sensor.

Abstract: System and processes for optimal selection and design of teeth for dentures based on the anatomical measurements and bite impressions of the patient. This information is applied in an iterative manner to rules that balance the anatomical, functional and aesthetic considerations to select the best teeth for a patient. The system may also use this information in an iterative manner to rules that balance the anatomical, functional and aesthetic considerations to design the optimal denture teeth and base for the patient as well.

Abstract: The invention relates to a method for the virtual post-processing of a first virtual three-dimensional dental model (14) of a dental prosthesis (28), said model having been created during the planning of the prosthesis (28). The first virtual dental model (14) is processed virtually after the planning stage in an additional method step (18, 31) by adapting at least one three-dimensional aesthetic surface structure (17) already in existence to the first dental model (14) by means of a virtual tool (10) with the aid of a computer (4) and a display device (6) and by subsequently inserting said structure into the first dental model (14). The aesthetic surface structure (17) has a predetermined form, size and/or a predetermined impression depth (41), and a tooth surface (19) of the dental model (14) is at least partially replaced by the adapted aesthetic surface structure (15, 17).

Abstract: A cradle, assembly, system and method for installing a prosthesis at a surgical site. The cradle temporarily engages the prosthesis and holds it in the correct orientation and position adjacent the surgical site. An aperture is defined in the cradle and a portion of the prosthesis is received therein. In one embodiment, the cradle, assembly and system are used to install a final dental prosthesis in a patient's mouth in a single visit to the dentist's office. A securement member pins the surgical template and subsequently the cradle to the jaw. A reinforced sub-structure on the final dental prosthesis is received in the aperture in the cradle. Cylinders attached to implants anchored in the jaw extend through holes in the sub-structure and are bonded to the prosthesis. The cradle is detached from the jaw and from the prosthesis prior to screws being re-inserted through the cylinders and into the implants.

Abstract: An extraoral dental scanner for three-dimensional capture of the surface of a dental shaped part (300) with a 3D measuring camera (102) having an optical axis (106), wherein the means for the machine-controlled relative positioning of the 3D measuring camera (102) and the dental shaped part (300) are embodied in such a way that the means for taking up and positioning the dental shaped part (300) can be moved into a parking position outside a region that can be captured optically by the 3D measuring camera (102), with a work plate (708) for manually positioning the dental shaped part (300) in the measurement volume (144) of the 3D measuring camera (102), wherein the work plate (708) is aligned perpendicularly to the optical axis (106) and wherein the work plate (708), as viewed from the 3D measuring camera (102), is arranged behind the means for taking up and positioning the dental shaped part (300), makes it possible to record uninterrupted 3D image data with very short recording times both by automatic and b

Abstract: A method for producing a dental model by means of a generative layering technique comprises the following steps: altering a three-dimensional CAD model of the dental model, wherein gap-like recesses are generated, such that the CAD model is cut into segments by the gap-like recesses, and connecting bridges are placed in the CAD model in such a way that the connecting bridges connect adjacent segments to each other, producing the dental model by means of a generative layering technique on the basis of the altered three-dimensional CAD model.

Abstract: The present technology relates to improved dental flosses and dental tapes and methods of improving oral hygiene and oral health. A dental floss according to the technology herein comprises expandable filament having a first end and a second end, wherein one or both of the first end or second end comprises a loop into which a human finger can be inserted, the expandable filament having a substantially rough outer surface.

Abstract: A one piece molded dental floss holder comprises an arcuate elongated handle terminating at a head at one distal end and a tapered pick end defined on an end of the handle opposite the head; a pair of spaced apart arms extending from the head, the spaced apart arms having a first end and a second end, the first end of the spaced apart arms adjoining the head of the handle; and a mushroom head floss element tie off on the top of the handle portion. The pair of spaced apart arms preferably includes visual operational references in the form of visible spiral grooves.

Abstract: The invention relates to an apparatus for irradiating an object, in particular for light-curing a dental object by means of a first radiation, the apparatus comprising at least one radiation source for emitting the first radiation, the apparatus further comprising at least one radiation sensor for measuring at least a second radiation, and the apparatus further comprising a housing. The second radiation is the first radiation reelected by the object.

Abstract: The present invention relates to method and system for bite registration using multiple bite registrations. In this method or system, when both the 3D teeth model of the upper jaw and the 3D teeth model of the lower jaw are successfully aligned with the bite surface, the bite surface with the 3D teeth models of the upper jaw and the lower jaw is displayed for further evaluation; the bite surfaces selected by the user are combined to generate a final bite registration. Using multiple bite surfaces for registration improves the accuracy.

Abstract: New bite-activated dental hygiene devices are provided. In one aspect, a high-speed tooth-cleaning device is provided, which is configured to be bitten down on by a user and which, when properly positioned, scrubs and flosses all of the user's teeth at once, without user-driven brushing. In other aspects of the invention, a device comprises bite-actuated tooth- and gum-brushing channels and other features facilitating the variable bite-actuated release and application of a dentifrice and scrubbing.

Abstract: A device and method to avert anal fecal leakage is disclosed that possess at least two means for the prevention of anal leakage or hemostatic application. The device is inserted internally and is used inside of the rectal cavity for absorption along with a sealing member placed externally against the anus which is designed as a secondary means for the prevention of leakage. An embodiment of the device includes a third sealing means to prevent leakage into the anal canal. The device is constructed to be flexible with a minimum of intrusiveness for the user during use. The device is constructed for one person insertion and removal unless patient or user is incapacitated. Due to its design, the device is capable for use over a wide range of human and certain animal applications.

Abstract: A tube assembly is disclosed which includes an elongated medical tube and a medical elongated body insertable in the medical tube and higher than the medical tube in rigidity and which is used in an assembled state with the medical elongated body inserted in the medical tube to be assembled together. The tube assembly further includes a puncturing section adapted to puncture a living body; a dissecting section adapted to dissect the living body as the puncturing section punctures the living body; and a rotation restraining section adapted to restrain the medical tube from rotating about its axis in relation to the medical elongated body in the assembled state.