Abstract: An electrosurgical device having a handpiece including a controller and an electrode assembly extending from the handpiece is disclosed. The electrode assembly includes a monopolar blade and a monopolar electrode. The monopolar blade includes a conductive element partially coated with an insulator and electrically coupled to the controller to selectively deliver a monopolar radiofrequency (RF) cutting signal. The monopolar electrode is spaced apart and electrically isolated from the monopolar blade. The monopolar electrode includes an exposed major conductive surface electrically coupled to the controller to selectively deliver a monopolar RF hemostatic sealing signal with a dispersed fluid.

Abstract: The invention relates to a photonic probe apparatus and a method for probing tissue to detect and mark biological tissue with cancerous or precancerous states. The apparatus involves a probe for illuminating tissue and collecting light from an illuminated tissue region through the probe, a unit for analyzing collected light to determine whether a threshold measure of probability of a cancerous or precancerous lesion in the probed tissue region in contact with the probe is exceeded, and an integrated tissue marking facility which can be activated to mark the probed tissue region through the probe when the threshold measure is exceeded. The photonic probe apparatus and the method are especially suitable for probing regions in squamous and columnar epithelia to detect and mark regions with cervical cancer or cervical intraepithelial neoplasia (CIN).

Abstract: A slip ring assembly is usable with a surgical shaft assembly. The slip ring assembly includes a first connector flange comprising a conductor. The slip ring assembly further includes a second connector flange comprising a conductive element in contact with the conductor, wherein the second connector flange is rotatable relative to the first connector flange. In addition, the slip ring assembly also includes a support member, wherein the second connector flange is sandwiched between the first connector flange and the support member, and wherein the support member is configured to apply a load onto the second connector flange to maintain the contact between the conductor and the conductive element.

Abstract: An end effector for a surgical instrument is disclosed. The end effector includes an ultrasonic blade and a jaw member including an asymmetric electrode comprising a first electrode and a second electrode. The first electrode defines a first width and the second electrode defines a second width. The first width is not equal to the second width. A first gap is defined between the first electrode and the ultrasonic blade and a second gap is defined between the second electrode and the ultrasonic blade. The first gap is not equal to the second gap.

Abstract: An electrode assembly for use with an electrosurgical instrument includes a pair of opposing jaw members and an electrode positioned on each jaw member. One or both of the electrodes includes a tissue contacting surface that has an outer periphery and defines a side surface depending therefrom. The tissue contacting surface and the side surface include a conjoining edge formed at a first predetermined angle that defines a first linear transition zone dimensioned to reduce arcing between the opposing jaw members during activation of the electrosurgical instrument.

Abstract: A surgical instrument includes a shaft having a proximal end and a distal end and end effector coupled to the distal end of the shaft. An electrical transmission conduit extends along the shaft from the proximal end to the distal end and is configured to deliver electrical energy to energize the end effector. A connector assembly electrically couples the electrical transmission conduit to the end effector, and the end effector is pivotably coupled to the connector assembly. In another aspect, a surgical instrument includes a pin, an electrically conductive connector including a contact portion and an attachment, the contact portion surrounding the pin. An electrical conduit is electrically coupled to the attachment of the connector. An electrically conductive jaw including an aperture is pivotable around the contact portion, and the contact portion electrically contacts the jaw at the aperture of the jaw.

Abstract: Systems and methods for tissue ablation. Systems include needles with deployable filaments capable of producing asymmetrical offset lesions at target volumes, which may include a target nerve. Ablation of at least a portion of the target nerve may inhibit the ability of the nerve to transmit signals, such as pain signals, to the central nervous system. The offset lesion may facilitate procedures by directing energy towards the target nerve and away from collateral structures. Example anatomical structures include lumbar, thoracic, and cervical medial branch nerves and rami and the sacroiliac joint.

Abstract: A surgical instrument for ablating tissue includes a handle portion and a shaft assembly extending distally from the handle portion. The shaft assembly includes an outer shaft, a coaxial cable extending through the outer shaft, and an electrode coupled to a distal portion of the outer shaft. The coaxial cable has a distal portion that forms a microwave antenna configured to transmit microwave energy radially outward and through the outer shaft. The electrode is configured to transmit radiofrequency energy. An actuation of the handle portion activates the transmission of the microwave energy from the microwave antenna and/or the transmission of the radiofrequency energy from the at least one electrode.

Abstract: The present disclosure relates to the field of tissue mapping and ablation. Specifically, the present disclosure relates to expandable medical devices for identifying and treating local anatomical abnormalities within a body lumen. More specifically, the present disclosure relates to systems and methods of focal treatment for overactive bladders.

Abstract: Various aspects of the present disclosure are directed toward apparatuses, systems, and methods for applying ablation therapy to a tissue region. The apparatuses, systems, and methods may include a balloon structure and one or more electrodes arranged on or within the balloon structure and configured to deliver energy to the tissue region.

Abstract: The present disclosure relates generally to medical devices, and more specifically to ablation catheters including bond joints formed to have improved strength and resistance to failure during use. In many embodiments an expanded bond-joint length and area and gap filling are used to increase the strength of the bond joint while decreasing relative variability. The bond joint length area is increased in a controlled manner so as to increase the overall strength of the bond joint by shifting the failure mode from the bond joint to a stronger area of the ablation catheter, such as the catheter shaft. Related methods of manufacturing such ablation catheters (or other medical devices including a bond joint) are also disclosed and described herein.

Abstract: A coupling mechanism includes a base and a lever. The base is configured to couple to an external fixture. The lever is pivotably coupled to the base and transitionable between a clamped configuration and an unclamped configuration. A first pair of opposed arms extends from the base and a second pair of opposed arms extends from the lever in opposed relation to the first pair of opposed arms. In the clamped configuration the second pair of opposed arms are proximate the first pair of opposed arms, and in the unclamped configuration the second pair of opposed arms are spaced apart from the first pair of opposed arms. At least one of the first pair of opposed arms or the second pair of opposed arms includes a step thereon. The step is configured to receive and retain a surgical tool therein in the clamped configuration.

Abstract: Minimally invasive methods and devices for endoluminally treating female fallopian tubes or male vas deferens of mammals are presented as a permanent method of contraception. In preferred embodiments, medical devices for male and female sterilization comprise laser radiation source operating at one or more preselected wavelengths between about 980 nm and about 1950 nm, preferably at least one of 980 nm, 1470 nm and 1950 nm; treatment waveguide with a radial or cylindrical radiation emitting tip; viewing scope; and a temperature sensor. In another preferred embodiment, a minimally-invasive permanent contraception method for males and females comprises the steps of introducing at least one treatment waveguide in a body cavity; positioning the treatment waveguide inside a body cavity; irradiating; and repeating the procedure in companion body cavity to inhibit fertilization.

Abstract: A light-diverting catheter tip is provided according to embodiments disclosed herein. The light-diverting catheter tip may be coupled with the distal tip of a laser catheter and divert at least a portion of the light exiting the distal tip of the laser catheter such that the spot size of the laser beam on an object after exiting the catheter tip is larger than the spot size of the light entering the catheter without the catheter tip. The catheter tip may be removably coupled with the catheter or constructed as part of the catheter. In other embodiment, the catheter tip may conduct fluid and/or divert fluid at the tip of the laser catheter.

Abstract: The present teaching relates to interactive medical image processing for surgical procedure planning. In one example, a three dimensional (3D) image of a kidney is obtained. The three dimensional image is rendered on a display screen. An input is received from a user specifying a location with respect to a representation of the kidney in the rendered three dimensional image. A representation of an instrument is rendered on the display screen based on the location. The instrument is automatically aligned with an infundibulum pathway of calyx at the location with respect to the kidney. A graphical line extension is rendered on the display screen to visualize the alignment of the instrument. One or more measurements related to the kidney are determined based on the location and an anatomical structure of the kidney.

Abstract: A method of planning path for a surgical instrument is provided for use during a surgical procedure. The method includes identifying a treatment target in images of a patient to be treated during a surgical procedure, determining dimensions of the patient, a surgical instrument, and an external obstruction, and determining a path to guide the surgical instrument to the treatment target during the surgical procedure. The surgical instrument is configured to be used during the surgical procedure. The external obstruction is an object external to the patient's body that interferes with one or more potential paths of the surgical instrument. The path is determined such that the surgical instrument avoids the external obstruction based on the determined dimensions of the surgical instrument and the determined dimensions of the external obstruction.

Abstract: Systems and methods are described herein to calculate implant orientation measurements of an acetabular cup implant in hip replacement surgery, such surgery performed with minimally invasive incisions. Surgeons may obtain real-time updated implant orientation measurements that compensate for pelvic tilt of a patient, such tilt measured pre-operatively. Implant orientation measurements may be measured from the patient's anterior pelvic plane, supine coronal plane, standing coronal plane or any other reference plane that the surgeon may find useful. Also disclosed are systems, methods and devices to measure hip center of rotation and provide leg length and offset measurements in hip replacement surgery.

Abstract: Devices and methods for visually confirming the positioning of a distal end portion of an illuminating device placed within a patient include inserting a distal end portion of an illuminating device internally into a patient, emitting light from the distal end portion of the illuminating device, observing transillumination resulting from the light emitted from the distal end portion of the illuminating device that occurs on an external surface of the patient, and correlating the location of the observed transillumination on the external surface of the patient with an internal location of the patient that underlies the location of observed transillumination, to confirm positioning of the distal end portion of the illuminating device.

Abstract: A method for performing a revision surgery using a robotic-assisted surgery system includes determining information related to an interface area between an implant component and a bone, and generating a planned virtual boundary associated with a portion of the interface area to be removed in a representation of the implant and the bone, based at least in part on the information related to the interface area. The method further includes tracking movement in the physical space of a cutting tool such that movement of the cutting tool is correlated with movement of a virtual tool, and providing a constraint on the cutting tool while the cutting tool removes the portion of the interface area. The constraint is based on a relationship between the virtual tool and the planned virtual boundary. The portion of the interface area is removed to remove the implant component from the bone.

Abstract: Apparatus for performing a procedure using a tool configured to be advanced into a skeletal portion within a body of a subject along a longitudinal insertion path, and for use with: (a) a 3D imaging device configured to acquire 3D image data of the skeletal portion. (b) a 2D x-ray imaging device that is unregistered with respect to the subject's body and configured, while a portion of the tool is disposed at a first location along the longitudinal insertion path.

Abstract: A system for accessing lesions or abnormalities using intra articular localization has an arm and a guide component. The arm with a localizing pin at a first end defines a virtual pathway. The guide component has a straight guide portion and a curved guide or arcuate portion. The curved guide or arcuate portion has a plurality of angularly spaced guide openings for passing a pin or drill or pin or punch along a selected path to form an entry access. The straight guide portion is for holding or coupling the arm at or in proximity to a second end of the arm. The selected path extends toward the virtual pathway to form the entry access using intra articular localization.

Abstract: A system for accessing lesions or abnormalities using intra articular localization, the system has a first arm with a localizing pin at a first end for defining a virtual pathway and a guide component. The guide component has a straight guide portion and a curved guide or arcuate portion. The curved guide or arcuate portion defines a second arm having a plurality of angularly spaced guide notches for locating a movable guide configured for passing a pin or drill or pin or punch held in the movable guide along a selected path to form an entry access. The straight guide portion has a plurality of notches for holding or coupling the first arm at or in proximity to a second end of the first arm. The selected path extends toward the virtual pathway to form the entry access using intra articular localization.

Abstract: An intraoral 3D scanner includes a probe light source configured to generate a probe light such that the probe light is transmitted towards the dental situation; a camera including an array of sensor elements, the camera being arranged such that the probe light from the dental situation is transmitted to the array of sensor elements, wherein the camera is configured to create images of the dental situation from which a point cloud is generated, and a guiding system configured to guide relative movement of the intraoral 3D scanner towards the dental situation, wherein the camera is part of the guiding system, the camera is configured to record images from which a relative position of the intraoral 3D scanner and the dental situation is determined, such that based on the relative position, the guiding system is configured to provide a positioning signal in the form of a positioning color code.

Abstract: A surgical robotic cart assembly includes a vertical column supporting a robotic arm thereon, a base, and a plurality of casters attached to the base and adapted to allow the surgical robotic assembly to move. The surgical robotic cart further includes at least one vacuum cup on the base for sealingly engaging the base to the floor thereby immobilizing the surgical robotic cart assembly.

Abstract: An instrument includes a chassis having a side adapted to be removably mated with a surgical robotic manipulator arm, a transport shaft coupled to the chassis, a valve including a valve channel and a movable valve member, a first robotic actuation piece, and a manual button. An auxiliary channel is defined in the chassis. A cavity extends through the transport shaft and intersects the auxiliary channel, which define an instrument axis. The valve channel intersects the auxiliary channel. The movable valve member translates across the valve channel along a valve member axis. The first robotic actuation piece is coupled to translate the movable valve member along the valve member axis and rotates about an actuation piece axis perpendicular to and offset from the valve member axis. The manual button is coupled to translate the movable valve member along the valve member axis and translates parallel to the valve member axis.

Abstract: An instrument comprises a flexible body comprising a proximal portion, a distal portion, and an inner sheath within the proximal portion. The inner sheath comprises a wall and a plurality of conduits extending through the wall within the proximal portion. A distal end of each conduit terminates proximal to the distal portion. The inner sheath further comprises a plurality of protrusions within the proximal portion. Each protrusion surrounds a portion of a corresponding conduit. The flexible body further comprises a steerable tube extending within the distal portion. The steerable tube comprises a wall and a plurality of grooves in the wall. The instrument further comprises a plurality of tendons extending from the proximal portion, beyond the distal ends of the plurality of conduits, and into the distal portion. In the proximal portion, each tendon extends through a corresponding conduit. In the distal portion, each tendon extends within a corresponding groove.

Abstract: Robot system includes robot main body including robot arm, end effector attached to robot arm, and force sensing device detecting force applied to end effector's tip end, actual reaction-force information generator generating force-sensing information according to force detected by force sensing device, and output force-sensing information as actual reaction-force information, virtual reaction-force information generator outputting force component detected by force sensing device, that has a magnitude proportional to time differentiation value, as virtual reaction-force information, adder configured to output information obtained by adding actual reaction-force information outputted from actual reaction-force information generator to virtual reaction-force information outputted from virtual reaction-force information generator, as synthetic reaction-force information, operating device outputting, when operator is made to sense a force according to synthetic reaction-force information outputted from adder and

Abstract: A robotic surgical system includes a controller, a surgical instrument supporting an end effector, and one or more connector members coupled to the end effector and movable to operate the end effector. Memory is operably coupled to the controller and is configured to maintain reference data of the one or more connector members. A sensor is secured to the one or more connector members and is disposed in electrical communication with the controller. The sensor is configured to register real-time data of the one or more connector members and communicate the real-time data to the controller. The controller is configured to compare the real-time data to the reference data and provide an output signal in response to a comparison of the real-time data to the reference data. A pair of connector members may be coupled to the end effector to impart three outputs.

Abstract: The invention, in one aspect, provides an electronic orientation monitor. The monitor includes an orientation sensing electronics configured for calibration when in a reference orientation and being responsive to manipulation of the monitor so as to calculate first, second and third angles which together represent a difference between a current orientation of the monitor and the reference orientation. The monitor further includes a display being responsive to the first and second angles so as to display a point positioned relative to first and second axes, the display being further responsive to the third angle so as to display a line having a direction relative to the first and second axes such that a combination of the position of the point and the direction of the line is indicative to a user of the difference between the current orientation of the monitor and the reference orientation.

Abstract: Medical procedure related objects (e.g., instruments, supplies) tagged with transponders (e.g., RFID transponders, dumb transponders) are accounted for via an accounting system using a number of antennas and interrogators/readers. The antennas and interrogators/readers are included on a cannula of the trocar so the tagged medical procedure related objects passing through the cannula are detected. A first set of antennas and RFID interrogator(s) interrogate a first portion of the cannula, such as proximate a proximal end at which the medical procedure related objects are introduced to the cannula. A second set of antennas and RFID interrogator(s) interrogate a second portion of the cannula, such as proximate a distal end at which objects exit the cannula for use in a medical procedure. A data store may maintain information including a current status or count of each supply, for instance, as entering or exiting the cannula.

Abstract: A lighting device for attachment to a handheld electrosurgical instrument is disclosed, which includes an elongated housing having opposed proximal and distal end portions and defining an interior chamber containing a battery powered light assembly for illuminating a surgical site, the housing having at least one smoke evacuation passage that extends from an inlet located adjacent to or near the distal end portion of the housing to an outlet located adjacent to or near the proximal end portion of the housing for removing smoke generated at the surgical site.

Abstract: Systems and methods for guiding a surgical procedure based on a surgical procedure plan may include an image capture device that captures one or more images of an exposed anatomical feature of a patient. These systems and methods may also include a computing device configured to receive a surgical procedure plan based on one or more desired attributes related to an anatomical 3D model representing the exposed anatomical feature of the patient. The computing device may register the anatomical 3D model to the exposed anatomical feature of the patient based on the one or more images of the exposed anatomical feature and a projector may further provide surgical guidance information to a surgeon based on the surgical procedure plan to facilitate performance of the surgical procedure.

Abstract: A dental instrument comprising a shaft and a working part adjoined thereto, with the working part having a coating in which abrasive bodies are embedded, is proposed, Firstly, the average proportion of the surface of the abrasive bodies which is covered by the coating can be at least 60%, preferably at least 65%, most preferably at least 70%. Secondly, the coating can, moreover, also consist of a nickel ahoy which additionally contains at least one element selected from the group consisting of titanium, vanadium, niobium, chromium, molybdenum, tungsten, manganese, iron and cobalt. In addition, a process for coating a working part, in particular for producing a dental instrument of this type, and also the use of such a dental instrument for cutting machining of solid bodies are proposed.

Abstract: The present disclosure relates to the field of endodontic instrumentation, and more particularly to apparatus and methods for manufacturing that include applying a variable heat-treat to an endodontic file blank based on geometric parameters that will be formed in the blank.

Abstract: An orthodontic appliance is disclosed and which cooperates with both the upper and lower dental arches of a patient and which includes an archwire coupler which is attached to individual archwires that are releasably attached to the anterior facing surface of a patient's teeth requiring orthodontic treatment; and a multiple section elongated telescoping assembly which is rotatably and releasably coupled to the archwires attached to the upper and lower dental arches of a patient undergoing treatment, and wherein the multiple section elongated telescoping assembly effects movement of the upper dental arch in a rearward direction, and the lower dental arch in a forward direction when the multiple section elongated telescoping assembly is in a given position along a predetermined course of travel.

Abstract: Systems for generating in-focus color images are provided. Related methods and devices are also provided.

Abstract: A method of fabricating a dental restoration is provided that includes the initial step of providing a powder of a dental material. An amount of a binder is then selectively deposited onto the powder of the dental material to produce an unfinished layer of the dental material. Multiple layers of the dental material are then produced by continually providing a powder of dental material and selectively depositing an amount of a binder until a three-dimensional unfinished model is produced. The unfinished model is then separated from an amount of unaffected powder, and is sintered to produce a three-dimensional dental restoration having a functionally-graded structure.

Abstract: Provided is a powder material for forming a three-dimensional object, the powder material containing granulated particles containing: a resin; and inorganic particles of which primary particles have a volume average particle diameter of 1 micrometer or less, wherein the granulated particles have a volume average particle diameter of 10 micrometers or greater but 70 micrometers or less and a BET specific surface area of 6 m2/g or greater but 8 m2/g or less.

Abstract: A dental floss holder includes a connecting section and at least four floss supporting arms extending from said connecting section. Each of the floss supporting arms has a first end and a second end. The first end is connected to the connecting section, and the second end includes a floss fastening portion for fastening a string of dental floss. The floss fastening portions of the at least four floss supporting arms are configured such that a string of dental floss attached to the floss fastening portions of the at least four floss supporting arms may be arranged to constitute the edges of a polyhedron.

Abstract: An oral care device for providing oral-cavity information to a user or a manager includes: a liquid supply unit; a mouthpiece connected to the liquid supply unit and including a spatial portion configured to accommodate at least one of an upper tooth side and a lower tooth side when the mouthpiece is inserted into an oral cavity; a pump connected to the mouthpiece and configured to suction liquid from the liquid supply unit and introduce the liquid into the spatial portion and to suction fluid from the spatial portion; a storage unit connected to the pump and configured to store or discharge fluid suctioned from the spatial portion; and a measuring unit connected to the storage unit and configured to measure a state of fluid stored in the storage unit, wherein liquid is introduced to the spatial portion from the liquid supply unit only by suction force of the pump.

Abstract: The mouthpiece includes an arch-shaped guard having an inner surface. The inner surface is contoured to follow a shape of a dentition. The arch-shaped guard is sized to span at least a portion of upper teeth and a portion of lower teeth in the dentition. The mouthpiece includes a bite plate positioned along the inner surface and dividing the arch-shaped guard into an upper and lower portion. The mouthpiece includes a first light array arranged along the lower portion of the arch-shaped guard, and a second light array arranged along the upper portion of the arch-shaped guard. The first and second light arrays are arranged at offset distances from the bite plate where the offset distance of the second light array is greater than the offset distance of the first light array. The first and second light arrays are arranged to direct light onto the upper and lower teeth, respectively.

Abstract: The present invention relates to an inhalation toxicity testing chamber device for nanoparticles having a plurality of concentrations. The present invention provides an inhalation toxicity testing chamber device for nanoparticles having a plurality of concentrations, which: can supply nanoparticles having different concentrations to particle exposure modules by stacking a plurality of particle exposure modules inside a single chamber housing and by allowing each particle exposure module so as to form an independent space from each other; can perform inhalation toxicity testing of nanoparticles having a plurality of concentrations through a single chamber housing by being capable of exposing the test animals put into each particle exposure module to nanoparticles having different concentrations; can easily perform inhalation toxicity tests of nanoparticles in a small scale laboratory etc.

Abstract: An incontinence clamp assembly includes a ring that may be worn on a penis. A tube is coupled to the ring. The tube is positioned on a bottom side of the penis having the tube being oriented perpendicular to the urethra. A stopper is slidably inserted into the tube and the stopper has a diameter that is larger than an inside diameter of the tube. The stopper is positioned in an open position having the stopper being positioned outside of the tube. In this way the stopper allows the urine to flow out of the penis. The stopper is positioned in a closed position having the stopper being positioned within the tube. In this way the stopper may compress the urethra thereby inhibiting urine from flowing out of the penis.

Abstract: A subcutaneous sling for neck lift surgery. The sling comprises a sling body, shaped to fit in a submental triangle of a patient undergoing neck lift surgery, comprising a narrow anterior edge for anchoring near the chin of the patient. The sling comprises two lateral sling extensions, each coupled to a respective side edge of two sides of the sling body, each projecting away from the center of the sling body in a posterior lateral orientation of between 45 and 90 degrees from the anterior-posterior axis, and curved slightly towards the narrow anterior edge to fit the submandibular triangle and extend to near each ear of the patient. The sling body is at least 4 centimeters long in the anterior-posterior dimension, and the ends of the two lateral sling extensions are at least 14 centimeters distant from each other.

Abstract: The invention relates to a resorbable multifilament comprising a number of individual resorbable filaments of a first type having a first degradation time and a number of individual resorbable filaments of a second type having a second degradation time, wherein the filaments of the first type and the filaments of the second type are arranged in close relationship to form a composite multifilament having a length and a specific composite cross-section comprising cross-sections of the individual filaments of the first type and second type, wherein the cross-sections of the individual filaments of the first and second type are located at determined relative positions, wherein the relative positions amongst the individual cross-sections of the filaments of the first and second types are invariant over the length of the composite multifilament.

Abstract: The present invention relates to a prosthesis for inguinal hernioplasty made up of a surgical mesh extending from a first end (6) to a second end (7) along a longitudinal direction (A) and comprising a first portion (1) that includes said first end (6), a second portion (2) that includes said second end (7) and a connecting portion (3) arranged between said first portion (1) and said second portion (2), wherein said first portion (1) has a substantially ring shape that is open or may be opened and is provided with a central hole (4), wherein said second portion (2) has a substantially elongated shape in said longitudinal direction (A), and wherein said connecting portion (3) has a width transverse to said longitudinal direction (A) smaller than the widths of said first portion (1) and said second portion (2) transverse to said longitudinal direction (A).

Abstract: An apparatus is configured to be implanted within a biological structure. The apparatus includes an annular retaining assembly and an occlusion member. The annular retaining assembly defines an annular opening and includes an outer ring and an inner ring. The outer and inner rings are disposed about a central axis. The outer ring also has an outer wall, an inner wall, and a bio-absorbable material. The inner ring defines an annular opening and is attached to the inner wall of the outer ring. The inner ring also includes a surface to promote tissue in-growth. The occlusion member extends from the annular retaining assembly toward the central axis. The occlusion member also includes a plurality of magnetics. The occlusion member is magnetically biased to a first position that substantially occludes the annular opening. The occlusion member is configured to elastically deform to a second position that substantially unblocks the annular opening.

Abstract: A stent for transluminal implantation comprises a first, second and third stent section for splinting and/or keeping open a hollow organ which are connected to each other via elastic tubular sections. The stent combines at least three different stent designs in one stent and can therefore be adjusted to the motion behavior of a hollow organ in an improved fashion.

Abstract: An endograft comprising a proximal end and a distal end is disclosed. The endograft includes a tube of biocompatible material. The tube includes a main lumen extending longitudinally from the proximal end to the distal end, the main lumen including a proximal portion, an intermediate portion and a distal portion; a branch lumen within the intermediate portion of the main lumen; and a seam, the seam extending longitudinally beside both the branch lumen and the distal portion of the main lumen, wherein the tube includes a lateral cross-section defining a tubular wall pinched together by the seam to form a branch portion. The branch portion includes an entrance within the intermediate portion of the main lumen and an exit through the tubular wall of the main lumen.

Abstract: An intraocular lens includes an annular housing coupled to a first window to form a lensing cavity. Disposed within the lensing cavity is two immiscible liquids, including a first liquid and a second liquid which form a meniscus at an immiscibility interface between the first liquid and the second liquid within the lensing cavity. The intraocular lens includes a flexible reservoir to store a variable portion of the first liquid. The flexible reservoir is disposed about at least a portion of a periphery of the annular housing. The intraocular lens also includes at least one channel linking the flexible reservoir to the lensing cavity to permit a transfer of the first liquid between the flexible reservoir and the lensing cavity. The transfer of the first liquid changes a curvature of the meniscus to adjust optical power of the intraocular lens.