Abstract: A sensor holder for retaining a dental radiation sensing device includes an elongated support member, at least one pair of retention guides attached to the support member, and at least one bite block attached to the support member. The retention guides are capable of holding an associated dental radiation sensing device. The bite block has a leading edge which is first inserted into a mouth of a patient and a trailing edge. The leading edge defining a recess into which structure within the mouth of the patient can seat. At least one of the retention guides may be moveable relative to the other retention guide.

Abstract: A filter assembly for use in a helical computed tomography system having an x-ray source for projecting x-ray beams along a projection axis is presented, the filter assembly including a first filter element for attenuating at least a portion of the x-ray beams, the first filter element constructed as a background-wedge for attenuating x-rays having a large aperture and a second filter element for attenuating at least a portion of the x-ray beams, the second filter element constructed to create a ridge. The second filter element may be rotated with respect to or adjusted in relation with or removed or replaced from the filter assembly to allow for adaptation to different helical pitch values.

Abstract: Systems and methods for reducing X-ray scatter during breast imaging, and more specifically during tomosynthesis imaging. In one embodiment, an anti-scatter grid having a plurality of septa may be configured to be positioned relative to an X-ray imaging device such that each septum of the plurality of septa extends along a direction substantially parallel to a coronal plane of a subject during imaging of the subject using the X-ray imaging device. The X-ray imaging device may be operable in a tomosynthesis mode for imaging of a breast of the subject and may include the anti-scatter grid disposed between a breast platform and the X-ray detector. The anti-scatter grid may be configured to move in a direction substantially parallel to a sagittal plane of the subject during tomosynthesis imaging.

Abstract: A radiation imaging system comprises a radiation generation unit configured to generate radiation, and at least one imaging unit configured to detect radiation from the radiation generation unit and obtain a radiation image, the imaging unit including a control unit configured to control to operate in one of a first operation mode of capturing the radiation image and controlling the radiation imaging system and a second operation mode of capturing the radiation image.

Abstract: An image processing apparatus of the present invention includes: a dynamic image acquiring unit acquiring a dynamic image; a time range setting unit setting a first time range and a second time range in an overall time of the dynamic image; a thumbnail generating unit generating a first thumbnail image and a second thumbnail image that are still images obtained by performing statistical processing on frame images in the first time range and frame images in the second time range, respectively; and a display unit displaying the first thumbnail image and the second thumbnail image so that they can visually be compared with each other.

Abstract: An X-ray imaging apparatus includes an X-ray generator configured to emit X-rays to a subject; an X-ray detection panel including a plurality of light receiving elements each configured to receive X-rays that have passed through the subject, convert the X-rays into an electric signal, and output the electric signal, and a plurality of capacitor modules respectively corresponding to the plurality of light receiving elements, each of the plurality of capacitor modules including a plurality of capacitors connected to a corresponding one of the light receiving elements and configured to store the electric signal output from the corresponding light receiving element in at least one capacitor of the plurality of capacitors; and an image processor configured to read out the electric signal stored in the at least one capacitor of each of the plurality of capacitor modules to generate at least one X-ray image.

Abstract: The invention relates to peripheral equalization during a mammography X-ray examination. High contrast tissue pixel values are removed from the background estimate by finding the minimum intensity values of the pixel located in the neighborhood, which have approximately the same distance to the skin line. Thus, high attenuating pixel values may be removed from the estimate and replaced by lower attenuating tissue pixel values. After a minimum filtration, a conventional peripheral equalization is performed. This may result in less overshoots and intensity values for higher attenuating structures in the peripheral region may become more consistent with intensity values for higher attenuating structures in the fully compressed region.

Abstract: A multi-modality cancer screening and diagnosis system is provided that allows cancer screening and diagnosis of a patient using at least two different and sequential three-dimensional imaging techniques without patient repositioning. The system includes a first three-dimensional image acquisition device, a second three-dimensional image acquisition device having a probe with a transmitter mounted thereon, and a positioning paddle for positioning and immobilizing an object to be imaged during the cancer screening and diagnosis procedure. The positioning paddle is designed to facilitate visualization of the breast in both three-dimensional modalities without movement of the patient, and preferably is designed to position the patient with comfort during a diagnosis procedure which uses both imaging modalities.

Abstract: The present invention relates to a monitoring apparatus (101) for monitoring an ablation procedure. The monitoring apparatus (101) comprises an ultrasound signal providing unit for providing an ultrasound signal that depends on received echo series of an object (4) that is ablated. The monitoring apparatus (101) further comprises an ablation depth determination unit (103) for determining an ablation depth from the provided ultrasound signal. The ablation depth can be determined directly from the ultrasound signal and is an important parameter while performing an ablation procedure. For example, it can be used for determining the progress of ablation within the object (4) and for determining when the ablation has reached a desired progression.

Abstract: The present invention discloses an ophthalmic device with a retinal vascularization monitoring system and associated methods. In some embodiments, the ophthalmic device can be a contact lens with a retinal vascularization monitoring system that can be used to monitor temporal changes of a pulsating vessel forming part of the retinal vascularization. Further, the retinal vascularization monitoring system may include elements for delivering a signal, including an audible and/or visual message, to the user that can be useful for identifying abnormal conditions such as a cardiac failure without delay. The audible and/or visual messages can be signals communicated to the user using one or both of the ophthalmic device and a wireless device in communication with the ophthalmic device.

Abstract: Embodiments of the present invention provide an ultrasound scanner equipped with an image data processing unit that can perform adaptive parameter optimization during image formation and processing. In one embodiment, an ultrasound system comprises a channel data memory to store channel data obtained by digitizing ultrasound image data produced by an image scan; an image data processor configured to process the stored channel data in the memory to reconstruct an ultrasound image for each of a plurality of trial values of at least one parameter to be optimized; and a parameter optimization unit configured to evaluate an image quality of the reconstructed ultrasound image for each trial value of the at least one parameter, and to determine the optimized value of the at least one parameter based on the evaluated image quality.

Abstract: An ultrasound probe connected to various diagnostic apparatuses and a method of operating the ultrasound probe. The includes transmitting an ultrasound signal to an object and receiving a response signal reflected from the object; acquiring information regarding a diagnostic apparatus connected to the ultrasound probe; determining a type of data that may be processed by the diagnostic apparatus based on the information regarding the diagnostic apparatus; generating transmission data corresponding to the determined type of data from the response signal; and transmitting the transmission data to the diagnostic apparatus.

Abstract: A biopsy device includes a cannula and an inner divider wall disposed in the cannula. The inner divider wall defines a plurality of cannula fluid openings. The outer wall of the cannula and the inner divider wall together define a cutter receiving lumen and a cannula vacuum lumen. The cannula fluid openings provide fluid communication between the cutter receiving lumen and the cannula vacuum lumen. A cutter is translatable with respect to the cannula for severing tissue drawn into the cannula. The cutter is operable to cover and/or uncover the cannula fluid openings. A proximal portion of the cutter is spaced away from the inner divider wall. A distal portion of the cutter is configured to slide adjacent to the inner divider wall.

Abstract: This invention relates to a device (10) for taking at least one sample of soft tissue from an organ, said device comprising a body (11) and a needle (12) formed by a stylet and a cannula coaxial with said stylet. The device comprises a mechanism for arming the needle, designed for sequentially moving the cannula and then the stylet from a rest position wherein the stylet and the cannula are extended towards the outside of the body, to a shooting position wherein the stylet and the cannula are retracted towards the rear of the body, and a triggering mechanism designed to release the stylet then the cannula and to allow their displacement from the shooting position to the rest position. The cannula is kinematically coupled to a cannula slider (24) comprising at least one retaining element (26) for maintaining the cannula slider in a shooting position.

Abstract: A biopsy device includes a needle extending distally from a body. The needle includes a transverse aperture, a first lumen, and a second lumen. A cutter is movable within the first lumen to sever tissue protruding through the transverse aperture. A valve assembly is operable to change the pneumatic state of the second lumen. The valve assembly includes a valve body and a translating member slidably disposed in a bore of the valve body. The valve body includes a first port and a second port. The first port is in fluid communication with the second lumen of the needle. The second port is in fluid communication with atmospheric air. The translating member selectively couples the first port with the second port based on the longitudinal position of the translating member within the bore. The translating member translates relative to the valve body based on the position of the cutter.

Abstract: Methods and devices for providing a biopsy device with a modified handle and stylet that provides a vacuum to be delivered to the targeted tissue for removal. The vacuum may draw the tissue into the notch where the tissue may then be severed via the cannula. Alternatively, the tissue may be drawn into to the notch after being severed via the stylet and/or cannula. The vacuum may be used to bring a larger amount of tissue into the notch than would otherwise be brought in the notch if no vacuum was used, providing a larger sample through the same size access point.

Abstract: A collapsible and expandable receptacle that can be inserted into a patient's cavity through a laparoscopic port (sleeve) is disclosed herein. The receptacle is configured so that when it enters the cavity it can be expanded or opened into a shape of a bowl or cone. A targeted tissue specimen can then be placed inside the expanded receptacle, and the surgeon has the room and visibility to cut the tissue with a power morcellator and avoid severing the bag or spreading unwanted particulate tissue to other areas inside the patient. Once the specimen has been cut and removed, the empty receptacle can be collapsed and removed out the same tissue removing sleeve.

Abstract: A medical implantable occlusion device is disclosed comprising a fabric of at least one thread and a structural formation thereof having a collapsed and an expanded shape, the formation comprises a proximal and a distal portion, a longitudinal axis extending between the proximal and distal portion, wherein at least one of the proximal and distal portions comprises a peripheral edge having a first and a second radius of curvature in a direction substantially perpendicular to the longitudinal axis, wherein the first radius of curvature is different from the second radius of curvature.

Abstract: A knee arthroplasty system for use in a patient's knee joint comprises a spacer block instrument including a base portion, a tibial component extending from the base portion and configured for placement against a tibia, and a femoral component configured for placement against a femur. The femoral component is rotatably coupled to the tibial component. The system further includes one or more spacer block shims structured for removable attachment to the tibial component.

Abstract: Cheek retraction devices including an upper frame element configured to bear against and retract soft oral tissue from one or more teeth of an upper dental arch, a lower frame element configured to bear against and retract soft oral tissue from one or more teeth of a lower dental arch. The upper and lower frame elements may each include left and right frame portions wherein the upper and lower left frame portions are joined to one another to form a v-shaped hinge on one side of the frame, while upper and lower right frame portions are joined to one another to form a v-shaped hinge on another side of the frame. The v-shaped hinges on opposed sides permit the upper and lower frame elements to be at least partially folded toward each other. A posterior frame element may be provided extending between the v-shaped hinges.

Abstract: A soft tissue fixation assembly includes a plurality of deformable bone anchors and a suture that is configured to fixedly attach to each of the bone anchors. One or more of the bone anchors can be inserted into a bone, and one or more of the bone anchors can be inserted through soft tissue and into the bone. The suture can be inserted through the bone anchors, and energy can be applied to the anchors, thereby causing a deformable material of the bone anchors to deform, thereby capturing the strand of suture in the bone anchor. The strand of suture can be placed in tension, and can extend over the soft tissue so as to retain the soft tissue in contact with the bone.

Abstract: An anchoring system is a combination of a nanofiber scaffold material and an arthroscopically deployable suture anchor. The anchor is deployed into a bone tunnel using common techniques. The nanofiber material extends out of the proximal end of the implant, once deployed. The implant also includes pre-loaded sutures or has the ability to accept and lock sutures to the implant. For an implant pre-loaded with suture, the implant is placed into the bone, the material is deployed above the anchor onto the surface of the bone, suture is passed through the soft tissue, and knots are tied to secure the tissue against the bone, sandwiching the material between the bone and tissue, to provide a pathway for cells from the bone marrow to the soft tissue-bone interface, promote the healing response, provide a biomimetic structure that cells readily adhere to, and create a larger healing footprint.

Abstract: An apparatus and method for affixing soft tissue to bone is provided. The apparatus comprises first and second arms including first and second jaws on distal ends. The second arm is mated to the first arm at a hinge located between the proximal ends of the first and second arms and distal ends of the first and second arms. To enter into an engaged position, the first and second arms pivot around the hinge such that the distal ends of the first and second arms close towards one another, and the proximal ends of the first and second arms move apart from one another. The engaged position causes the first jaw on the distal end of the first arm and the second jaw on the distal end of the second arm to compress and hold soft tissue.

Abstract: A suture device is provided with a longitudinal member; a pair of grasping members; a suture needle; a power transmitting member; an opening-closing operating portion; a pair of needle locking portions having a first needle locking member and a second needle locking member and locking or releasing the suture needle to or from the pair of grasping members; a pair of wire members connected to the pair of needle locking portions; a needle locking and operating portion that operates the pair of wire members; a link member having a first end and a second end connected to the pair of wire members; and rotatable support portions that rotatably support the link member.

Abstract: A device for making continuous suture stitches including a handle and a device head. The handle including a power source for the device head and a means for attachment to the device head. The device head including a suture thread supply; a needle rotationally movable, operable for moving the thread through a tissue; a hook operable for hooking and lifting the thread in automatic coordination with the needle; and a catcher operable for moving the thread into and out of the hook in automatic coordination with the hook; thereby providing a device for making continuous suture stitches for adjoining a first edge and a second edge of a tissue in an edge-to-edge interface.

Abstract: An orthopedic staple includes a bridge portion having a pair of ends and a staple leg formed from a shape memory material connected to each of the pair of ends. The staple legs have a constrained position where the staple legs are generally parallel to one another and a relaxed position where the staple legs generally converge toward one another. Each of the staple legs has a protruding portion with a maximum leg thickness and a tip, with each of the staple legs increasing in thickness from the tip to the protruding portion. The bridge portion and each of the protruding portions define grasping portions therebetween that are configured to provide resistance to backout of the orthopedic staple.

Abstract: A surgical instrument for surgically joining a tissue includes a handle assembly, an elongate portion extending distally from the handle assembly, a pair of opposed jaw members, and a tissue stop. The tissue stop is mechanically engaged with a first jaw member and is configured to retain the tissue between the jaw members. The tissue stop is movable between a first position, where a stopping portion of the tissue stop is disposed between a tissue-contacting surface of the first jaw member and a tissue-contacting surface of the second jaw member, and a second position, where the stopping portion is between the tissue-contacting surface of the first jaw member and a lower surface of the first jaw member. A portion of the tissue stop is made of stamped metal section and a portion of the tissue stop is made of an overmolded plastic section.

Abstract: An electrically powered surgical instrument includes a surgical end effector having a surgical procedure effecting actuation assembly. A handle is coupled with the end effector. An electric motor is disposed within a shell of the handle and has power terminals and a drive train actuating the assembly when the motor is supplied with power. A break-before-make power supply switch at the handle selectively controls supply of power to the motor. A post-termination braking circuit electrically short-circuits the power terminals when the switch does not supply power to the motor. A method for post-termination braking of an electrical motor utilizes the permanent magnetic field of the motor to counteract an inertia-induced over-stroke characteristic of the motor, drive train, and/or actuation assembly after powered operation by short-circuiting the still-spinning motor to create an electrically generated magnetic field in opposition to the permanent magnetic field upon ceasing supply of power to the motor.

Abstract: A surgical stapling apparatus for progressively stapling and forming an incision in body tissue is provided. The apparatus includes a body portion and a tool assembly supported on the body portion. The apparatus further includes an input cam member slidable within the body portion, a drum member rotatably supported within the body portion, and an output cam member slidable within the body portion. The drum member is coupled to the input cam member such that linear movement of the input cam member effects rotatable movement of the drum member. The output cam member is coupled to the drum member such that rotatable movement of the drum member effects linear movement of the output cam member. Linear movement of the input cam member effects movement of an anvil in relation to a cartridge between unclamped and clamped positions.

Abstract: A surgical instrument assembly can comprise a handle including an electric motor, a shaft assembly including a drive member, and a magnet configured to generate a magnetic field. The surgical instrument assembly further comprises, one, a rotatable output shaft operably coupled with the electric motor and the drive member and, two, a wire coil wound around the output shaft which is positioned in the magnetic field. The wire coil is rotated within the magnetic field when the output shaft is rotated about a longitudinal axis which induces a current in the wire coil. The surgical instrument assembly further comprises a strain gauge mounted to the output shaft configured to detect strain created within the output shaft and, in addition, a circuit mounted to the output shaft, wherein the circuit and/or the strain gauge is powered by the current induced in the wire coil.

Abstract: Improved tissue fasteners are disclosed that can be inserted into (and optionally through) tissue structures underlying a tissue surface for affixing overlapping tissues and tissue planes together, and the like. In some embodiments, an elongate anvil body may protrude distally and/or laterally from a fastener support disposed along the base. The anvil body may have a sharpened end and be configured to penetrate into the tissue, with the elongate anvil body optionally having a bend from a more distal orientation adjacent the clip support to a more lateral orientation adjacent the sharpened end during at least a portion of the deployment. The first leg can be driven through a desired location on the surface of the first tissue and against a receptacle of the anvil body so as to deform the fastener and affix it to the first tissue.

Abstract: A stapling assembly configured to be operably attached to a surgical system comprises a carrier operably supporting a cartridge assembly therein and an anvil. The stapling assembly further comprises a housing removably attachable to the surgical system and an axial drive assembly. The stapling assembly further comprises a motor supported within the housing, wherein the motor is operable to selectively transmit a rotary motion to the axial drive assembly. The motor can only transmit the rotary motion to the axial drive assembly when the housing is coupled to the surgical system and a power source is selectively coupled with the motor.

Abstract: A surgical stapling assembly comprises a housing, wherein the housing comprises an engagement member for removably coupling the housing to a surgical system. The surgical stapling assembly further comprises a first jaw and a second jaw. The surgical stapling assembly further comprises a drive member and a motor positioned in the housing, wherein the motor is operable to selectively move the drive member. The surgical stapling assembly further comprises at least one electrical contact supported by the housing, wherein the at least one electrical contact is operable to supply power from a power source to the motor only when the housing is operably attached to the surgical system.

Abstract: A stapling assembly for use with a stapling system comprises a mounting portion and an elongate shaft. The stapling assembly further comprises a cartridge body and a firing member. The stapling assembly further comprises a motor drive and a power input configured to supply power to the motor drive. The stapling assembly further comprises a first powered state prior to the staple firing stroke and a second powered state in which the power input supplies power to the motor drive to perform the staple firing stroke.

Abstract: The application discloses devices, delivery tools, systems, and methods for treating biliary disease. Device comprise, for example, a component configured for deployment between a gallbladder and location within a gastrointestinal tract of a patient which has a proximal end and a distal end with a lumen extending therethrough. A method of deploying the device can be achieved by, for example, creating a duct or fistula between a gallbladder lumen and a portion of a gastrointestinal tract; and providing for drainage from the gallbladder to the gastrointestinal tract.

Abstract: An anvil (300) for use in connection with a first member (10) of an anastomotic device (100) in the side wall of an intestine is provided. The anvil (300) comprises a distal head portion (301) and a connecting rod (302) extending proximally from the head portion (301). The distal head portion (301) has a first member retaining means (304), being displaceable laterally and centrally between a first member locking position and a first member releasing position. A tool (400) for use in connection with an anvil (300), according to above, is also provided, and a kit of parts comprising the two. The tool (400) comprises a receiving member (401) for receiving the connecting rod (302) of the anvil (300), and a seat (405) for a second member (20) of the anastomotic device (100), said seat (405) being arranged circumferentially of said receiving member (401), and said receiving member (401) being displaceable in relation to said seat (405).

Abstract: An intra-vascular aneurysm-treatment stent and a method for lowering pressure within an aneurysm bubble in a blood vessel. A stent coil is insertable into a blood vessel, the coil made of a material sufficiently flexible to move around curves, loops, and corners in the blood vessel. The stent coil is positioned in the blood vessel with selected stent coil portions proximate an opening into either a saccular aneurysm or a fusiform aneurysm. Blood in the lumen of the blood vessel flows past the leading edges and both over the outer surfaces, and under the inner surfaces. A portion of the blood inside the aneurysm becomes entrained with the blood flowing over the outer surfaces. At the trailing edges, the converging blood flows create eddies.

Abstract: A device for closing a left atrial appendage of a patient comprising a containment member having a first configuration for passage into the left atrial appendage and a second larger configuration, and a wire movable into the containment member in situ to expand the containment member in the left atrial appendage to the second configuration.

Abstract: An occlusion clamp including: (a) an occlusion tongs including a primary spring coupling a first longitudinal arm to a second longitudinal arm, the first longitudinal arm including a first linear occlusion surface configured to be parallel to and overlap a second linear occlusion surface of the second longitudinal arm, each of the first and second longitudinal arms having a free distal end; and, (b) a secondary spring removably coupled to the occlusion tongs.

Abstract: An occlusion clip comprising: (a) a first elongated occlusion arm; (b) a second elongated occlusion arm; (c) a first elongated biasing arm coupled to a distal portion of the first elongated occlusion arm; (d) a second elongated biasing arm coupled to a distal portion of the second elongated occlusion arm, where a proximal portion of the first elongated biasing arm is coupled to a proximal portion of the second elongated biasing arm, where the first elongated occlusion arm extends parallel to the first elongated bias arm along a majority of its length, and where the second elongated occlusion arm extends parallel to the second elongated bias arm along a majority of its length.

Abstract: A resection guide locator includes a bone engagement portion with surfaces that are complementary to the surface topographies of a bone to be resected during surgery. A housing includes a socket defined by a resilient annular wall that is sized and arranged so to accept a resection guide by press-fit to thereby position and hold the resection guide within he socket. The resection guide is maintained in a predetermined, preferred position while the surfaces are releasably locked in position on the bone. A method is disclosed for forming and using the resection guide locator.

Abstract: An orthopedic impacting tool comprises a motor, a linear motion converter, an air chamber, a compression piston, an impacting element, an anvil element, and a broach adapter. The compression piston may cause the impacting element to apply controlled force on a broach adapter to create a precise opening for subsequently disposing a prosthesis in a patient. The tool allows forward or backward impacting for expanding the size or volume of the opening or for facilitating removal of the broach and tool from the opening. A force adjustment control of the tool allows a user to increase or decrease the impact force. A light source and hand grips improve ease of operation of the tool.

Abstract: The present invention relates to medical apparatuses and procedures for reconstructing a ligament. There is provided a trephine (10) comprising an adaptor (11), an elongate reamer (12) coupled thereto, and a reamer support stem (13), wherein the reamer support stem is mounted concentrically within the reamer and adaptor, and wherein at least a portion of the reamer support stem is slidably moveable about a longitudinal axis of the trephine.

Abstract: Systems and methods for monitoring an operative site during a surgical procedure using a computer controlled surgical device. In general the methods include the steps of processing one or more defined cutting paths having one or more cut regions; determining a correlation between the cut region and one or more critical regions to generate an alert, wherein the alert indicates a movable end-effector is within a defined proximity of the critical region; and requiring a user acknowledgment of the alert to allow processing of the cutting path to continue. Also described herein are systems and methods for minimizing user fatigue during a semi-computer controlled surgical procedure. In general the methods includes the step of requiring a user generated acknowledgment in response to a computer generated alert, wherein the user acknowledgment is generated using a user controller, the user controller being minimally intrusive to the user experience.

Abstract: The foreign matter capture instrument includes: a first manipulation wire; framework wire materials, the base end parts being coupled to a leading end part of the first manipulation wire, and the leading end parts being respectively bundled together; and a second manipulation wire which is coupled to the leading end parts of the framework wire materials, separates from the first manipulation wire extending toward the base end side of the first manipulation wire. By moving the first manipulation wire toward the leading end side relative to the second manipulation wire, the framework wire materials expand and configure a basket, and by further relatively moving the first manipulation wire toward the leading end side, the basket becomes shallower.

Abstract: An ultrasonic instrument comprises a body, a shaft assembly, an ultrasonic blade, and a pivoting member. The shaft assembly extends distally from the body. The ultrasonic blade is positioned distal to the shaft assembly. The pivoting member is pivotable with respect to the blade from an open position to a closed position to thereby clamp tissue between the pivoting member and the blade. The shaft assembly comprises a feature to provide for the removal of surgical debris (e.g. tissue, coagulated blood, etc.), body fluid, etc. from the shaft assembly. The feature may remove the surgical debris, body fluid, etc. from a cavity within the shaft assembly. The feature may also prevent the collection of surgical debris, body fluid, etc. within the shaft assembly.

Abstract: An ultrasonic clamp coagulator assembly that is configured to permit selective cutting, coagulation and clamping of tissue during surgical procedures. An elongated portion of the instrument can be configured for endoscopic applications and has an outside diameter of less than 6 mm. The construction includes a clamping mechanism, including a clamp arm pivotally mounted at the distal portion of the instrument, which is specifically configured to create a desired level of tissue clamping forces, exceeding 4 pounds when the trigger is fully closed. The clamping mechanism includes a force-limiting mechanism that effectively smooths out abusive tissue forces.

Abstract: An ultrasonic instrument comprises a handle assembly configured to receive an ultrasonic transducer, a shaft assembly having an acoustic waveguide and an ultrasonic blade, and a retractable clamp arm. The ultrasonic blade is in acoustic communication with the acoustic waveguide such that the ultrasonic transducer is operable to drive the ultrasonic blade to vibrate ultrasonically via the acoustic waveguide. The clamp arm is configured to selectively translate between an inoperative position and an operative position. The clamp arm is positioned generally proximal to the ultrasonic blade when the clamp arm is in the inoperative position. The clamp arm is positioned lateral to the ultrasonic blade when the clamp arm is in the operative position. When in the operative position, the clamp arm is operable to move toward and away from the ultrasonic blade so as to capture and compress tissue between the clamp arm and the ultrasonic blade.

Abstract: A catheter assembly includes a catheter body having a catheter lumen. A manifold assembly is coupled with a proximal catheter portion. A manifold lumen extends through the manifold assembly, and the manifold lumen includes an assembly cavity extending around the proximal catheter portion. A fluid jet loop is coupled with a high pressure tube at a distal catheter portion. The catheter assembly further includes a tapered loop guide surface.

Abstract: A medical device is presented for use in tissue characterization and treatment. The device comprises: a tissue characterization probe comprising an elongated carrier for carrying an array of tissue characterization sensors arranged in a spaced-apart relationship at least along an axis of said carrier, such that progression of the probe through a tissue mass provides for locating and determining a dimension of an abnormal tissue specimen inside said tissue mass based on characterization signals from the sensors in the array, thereby enabling consequent treatment of the abnormal tissue specimen by a treatment tool.