Abstract: Methods of reprocessing physiological sensors may include applying heat to a physiological sensor so as to efficiently remove adhesives, adhesive layers, and/or other disposable components of the sensor. Heat may be applied to the physiological sensor efficiently via a medium, such as an aqueous solution (for example, water). Reusable components of the physiological sensor may then be reassembled with new disposable components and/or adhesives to produce a reprocessed sensor. The methods may further include testing and/or replacement of various reusable sensor components, testing of the reprocessed sensor, cleaning of the reprocessed sensor and/or sensor components, and/or sterilization of the reprocessed sensor, among other steps.

Abstract: A safety needle device includes a housing including a passageway with a needle cannula extending therefrom. A shielding member is movable between a first position in which a puncture tip of the needle cannula is exposed therefrom and a second position in which the puncture tip of the needle cannula is encompassed therein. The shielding member is maintained in the first position against a biasing force which biases the shielding member toward the second position. A fluid and/or a temperature activation material is associated with the shielding member and is adapted to deform upon contact with a fluid medium and/or a certain temperature or temperature range. The fluid medium flowing through the needle cannula causes the fluid activation material to deform, such as through expansion, thereby releasing the shielding member from the first position and allowing a drive member to bias the shielding member toward the second position.

Abstract: Various embodiments of the present invention describe mechanisms configured to monitor, track, and manage symptoms of Parkinson's disease (PD). According to particular exemplary embodiments, a system includes sensors configured to monitor motion exhibited by a user having symptoms of Parkinson's disease, a processor configured to determine whether the motion constitutes a tremor episode, and memory configured to maintain data associated with the tremor episode, a severity rating associated with the tremor episode, and medication intake information. In exemplary embodiments, the effectiveness of a user's medication intake can be determined based on data displayed regarding severity rating variations over time in relation to medication intake.

Abstract: Various embodiments of the present invention describe mechanisms configured to monitor, track, and manage symptoms of autism spectrum disorder. According to particular embodiments, a system includes sensors configured to monitor repetitive motion exhibited by a user with an autism spectrum disorder (ASD). The sensors are connected to a processor that is configured to determine whether the repetitive motion exhibited by the user exceeds an autism episode threshold. Once the autism episode threshold has been reached, the processor can access from memory an autism episode alleviation action associated with the user. Materials associated with the autism episode alleviation action can be presented to the user through an output interface, such that presentation of these materials is configured to reduce the severity or duration of the autism episode.

Abstract: Some embodiments described herein relate to receiving lactate concentration data from a non-invasive sensor. A ratio of aerobic to anaerobic exertion can be determined based on the concentration of lactate, and real-time feedback can be provided based on the ratio of aerobic to anaerobic exertion. For example, the user can be encouraged to maintain a level of intensity in which he or she approaches (but does not exceed) maximal oxygen consumption.

Abstract: The invention provides a neck-worn sensor that is a single, body-worn system that measures the following parameters from an ambulatory patient: heart rate, pulse rate, pulse oximetry, respiratory rate, temperature, thoracic fluid levels, stroke volume, cardiac output, and a parameter sensitive to blood pressure called pulse transit time. From stroke volume, a first algorithm employing a linear model can estimate the patient's pulse pressure. And from pulse pressure and pulse transit time, a second algorithm, also employing a linear algorithm, can estimate systolic blood pressure and diastolic blood pressure. Thus, the sensor can measure all five vital signs along with hemodynamic parameters. It also includes a motion-detecting accelerometer, from which it can determine motion-related parameters such as posture, degree of motion, activity level, respiratory-induced heaving of the chest, and falls.

Abstract: An intravascular sensor assembly including a flexible elongate member having a longitudinal axis (LA) is provided. The sensor assembly includes a first engagement feature proximal to a distal end of the flexible elongate member; a core member disposed inside a lumen of the flexible elongate member, the core member configured to translate within the flexible elongate member along the LA proximal to the first engagement feature; and a component holding a sensor circuit, the component fixedly secured to a distal end of the core member such that the mounting structure translates along the LA of the flexible elongate member with the core member. A system and a method for performing measurements using a sensor as above are also provided.

Abstract: In an example, an electrical circuit device for amplifying a physiological signal includes a modulation unit configured to receive an input signal, to modulate the input signal to produce a modulated signal. The device also includes an amplification and transconductance unit configured to amplify an amplitude of the modulated signal and increase a transconductance of the modulated signal to produce a transconductance enhanced modulated and amplified signal, where the amplification and transconductance unit comprises at least a first complementary pair of transistors and a second complementary pair of transistors configured to receive the modulated signal and to amplify and increase the transconductance of the modulated signal. The device also includes a demodulation unit configured to receive the transconductance enhanced modulated and amplified signal and to demodulate the signal.

Abstract: A prosthesis for monitoring a stenosis in the prosthesis comprises a tubular prosthesis having a proximal portion, a distal portion, and a lumen extending therebetween. A sensor is coupled to the tubular prosthesis and disposed at an effective predetermined location on the tubular prosthesis so that the sensor may sense a presence of the stenosis in the lumen.

Abstract: A method and system for cancelling body movement effect for non-contact vital sign detection is described. The method begins with sending on a first electromagnetic wave transceiver a first electromagnetic signal with a first frequency to a first side of a body, such as a person or animal. Simultaneously using a second electromagnetic wave transceiver a second electromagnetic signal is sent with a second frequency to a second side of a body, wherein the first frequency and the second frequency are different frequencies. A first reflected electromagnetic signal reflected back in response to the first electromagnetic wave on the first transceiver is received and a first baseband complex signal is extracted. Likewise a second reflected electromagnetic signal reflected back in response to the second electromagnetic wave on the second transceiver is received and a second baseband complex signal is extracted.

Abstract: A method and system for identifying location of a touched body part. The method includes initializing a tracking system for monitoring travel of a pointer useful for indicating a touching operation, wherein the touching operation is performed on a body part. In addition, the method includes monitoring the travel of the pointer from a predetermined first location to a second location, wherein the second location coincides with a touch endpoint on a body part; and identifying the location of body part that was touched by the pointer.

Abstract: A patient monitor system (10) includes a signal processor (30) which analyzes signals from physiological parameter sensors (20) to derive physiological data values, plots, and alarms. A display (12) displays physiological values and plots (42). An advisor engine, routine, or processor (34) is connected with the signal processor to analyze at least alarm occurrences, also in combination with user interactions, and provide directly actionable advice for reducing alarm frequency which is displayed unobtrusively on the display. The directly actionable advice includes specific actions or adjustments which are specific to a current patient, a present situation, or a present mode or setting of the patient monitor system. The unobtrusively displayed directly actionable advice is displayed without the use requesting it.

Abstract: A method for image acquisition includes selectively concealing and exposing an x-ray source to a target object while the x-ray source travels along a first path, virtually moving an x-ray detector along a second path in a first direction while the x-ray source is exposed to the target object, and virtually moving the x-ray detector along the second path in a second direction generally opposite the first direction while the x-ray source is concealed from the target object.

Abstract: A method includes performing a contrast enhanced computed tomography (CT) scan of tissue of interest of a subject, with an imaging system (100) having a radiation source (112) and a detector array (118), in which a peak contrast enhancement of the tissue of interest, a full range of motion of the tissue of interest, and an entire volume of interest of the tissue of interest are concurrently imaged during a single rotation of the radiation source and the detector array of the imaging system over an entire or a predetermined sub-portion of a breathing cycle.

Abstract: A radiographic imaging apparatus having a detector, a radiation source array, and a control processor is configurable to individually energize the radiation sources. A collimator having a number of apertures is movable to either a first or second position in a path of the radiation source array. In one position, the apertures are aligned with a first subset of the radiation sources. In another position, the apertures are aligned with a second subset of the radiation sources. The second subset of the radiation sources define substantially the same radiation field that is defined by the first subset of the radiation sources. A transport apparatus translates the collimator member between at least the first and second positions according to an electronic instruction.

Abstract: Disclosed herein is a method and apparatus for operating an X-ray image processing system of creating a panoramic image based on three-dimensional (3D) Computed Tomography (CT) image data and displaying the panoramic image on the display unit, receiving a part of an object to be measured in the panoramic image through the input unit, and calculating an actual 3D length of the part of the object based on depth information of the CT image data and displaying the actual 3D length on the display unit. The part of the object can be selected by the user to measure a length of a desired part.

Abstract: Various methods, systems and apparatus are provided for brain imaging during virtual reality stimulation. In one example, among others, a system for virtual ambulatory environment brain imaging includes a mobile brain imager configured to obtain positron emission tomography (PET) scans of a subject in motion, and a virtual reality (VR) system configured to provide one or more stimuli to the subject during the PET scans. In another example, a method for virtual ambulatory environment brain imaging includes providing stimulation to a subject through a virtual reality (VR) system; and obtaining a positron emission tomography (PET) scan of the subject while moving in response to the stimulation from the VR system. The mobile brain imager can be positioned on the subject with an array of imaging photodetector modules distributed about the head of the subject.

Abstract: An x-ray recording system contains an x-ray emitter for generating a beam used for imaging, an imaging x-ray detector with a two-dimensional or three-dimensional recording geometry for determining the attenuation of the rays of the beam, a patient bearing and/or positioning device for a patient in a recording region of the x-ray recording system between the x-ray emitter and the x-ray detector. A time of flight (TOF) camera is arranged for establishing the contour of the patient and a computer with a memory and software stored therein is present, which computer unit is embodied, during operation, to generate a three-dimensional wire model of the patient with joint locations arranged therein from the contour of the patient recorded by the TOF camera and to simulate and display at least one anatomical structure scaled to the wire model.

Abstract: In an X-ray CT apparatus, an annular rotating body includes an X-ray tube and an opening portion accommodating a radiator that discharges heat from the X-ray tube and into which a bed can be inserted. A stand includes a frame disposed in a rear portion of the annular rotating body, and supports the annular rotating body to be rotatable about an axis. A cover which covers the annular rotating body and the stand includes an exhaust port. A cooling mechanism, disposed at a position away from a position of the exhaust port along a circumferential direction of the annular rotating body between an outer circumferential surface of the annular rotating body and cover, includes a fan disposed at the stand. A duct receives exhaust air from the fan at a rear position of the fan between the frame and cover, and leads from the fan to the exhaust port.

Abstract: An X-ray CT apparatus includes: intensity distribution data acquiring circuitry is configured to acquire, by performing a first scan, intensity distribution data of X-rays being radiated from an X-ray tube and having passed through a subject; scan controlling circuitry is configured to estimate an X-ray dose with which it is possible to discriminate individual X-ray photons having passed through the subject based on the intensity distribution data and to cause a second scan that is for a photon counting CT purpose to be performed by causing the estimated dose of X-rays to be radiated from the X-ray tube to the subject; a counting result acquiring circuitry is configured to acquire, by the second scan, a counting result by counting the X-ray photons being radiated from the X-ray tube and having passed through the subject; and an image reconstructing circuitry is configured to reconstruct X-ray CT image data based on the counting result.

Abstract: The present invention is capable of distinguishing four types or more of substances such as air, water (soft tissues), contrast medium, and bones (calcification) to diagnose progress of atherosclerotic sites using dual energy imaging. A subject is imaged with two types of different tube voltages and an image obtained by image reconstruction is binarized to carry out a reprojection process; thereby, the distance of penetration of air is estimated, the contribution of air in measurement projection data is determined, and the amount of reduction by the air is deducted from the projection data so as to enable distinction between four or more substances such as air, water (soft tissues), contrast medium, and bones (calcification).

Abstract: To improve use convenience to the user who executes imaging work in an imaging environment where plural X-ray generating apparatuses exist, a control apparatus for controlling X-ray irradiations performed by the plural X-ray generating apparatuses has: an obtaining unit for obtaining identification information for uniquely identifying one X-ray generating unit of the plural X-ray generating units, which is specified as a control target which is allowed to emit X-rays; and a control unit for, based on the obtained identification information, controlling so that, for a period of time during which the one X-ray generating unit is specified as the control target, processes regarding the X-ray irradiations by the other X-ray generating units are restricted.

Abstract: The invention relates to a model for use in an imaging technique based on an interaction of the model with an electromagnetic radiation. The model comprises a plurality of volume elements. The interaction intensities of two neighboring volume elements are distinguishable by an imaging technique. The model comprises first volume elements made of a supporting material, and second volume elements are made of a supporting material and a contrast material and exhibit a higher interaction intensity with the electromagnetic radiation than the first volume elements because of the presence of contrast material. The second volume elements have been generated by a printing method. The invention further relates to a method for fabricating the model by 3D printing.

Abstract: A phantom for use in quality control of tomographic images, the phantom including a cylindrical plate made of a uniform material having a density d1, with two cylinders being inserted in the plate, the cylinders being made out of uniform materials having different densities d2, d3, the density of one of the cylinders being greater than the density d1 of the plate, and the density of the other cylinder being less than the density d1 of the plate, and including a first series of pairs of holes of different diameters drilled in the plate, the axes of the holes of the first series being oriented axially relative to an axis of revolution of the plate, and the holes in a given pair being spaced apart from each other by a distance equal to their diameter.

Abstract: Disclosed herein are techniques for joint performance monitoring and diagnosis. A joint monitoring system includes a plurality of event detection sensors configured to be mounted on a wearer of the joint monitoring system, and a plurality of position tracking sensors configured to be mounted on the wearer. The plurality of event detection sensors is configured to generate detection signals for detecting an event in a joint region. The joint region includes a region within a body of the wearer and within a threshold distance of a joint. The detection signals from the plurality of event detection sensors includes information for determining a location of the event. The plurality of position tracking sensors is configured to record position information of one or more body parts associated with the joint in response to the detected event.

Abstract: Disclosed is a process for displaying ultrasound data representative of a rotationally symmetrical contractible chamber or vessel within a patient which involves obtaining ultrasound data from the ultrasound imaging of the vessel or chamber through at least a phase of one cardiac cycle and virtually sectioning the vessel or chamber into multiple circumferential segments, each extending its own longitudinal distance from a common reference point. The data is used to obtain rotational parameters representative of an entire circumferential segment of the chamber or vessel. The process is repeated until a rotational parameter for each entire circumferential segment along a desired distance of the longitudinal axis of the chamber or vessel has been obtained. The rotational parameters are displayed in a two dimensional format having annular rings with each annular ring being representative of a given circumferential segment.

Abstract: Ultrasound apparatus or techniques can include obtaining reflected ultrasound echo information, which can be used to construct a two-dimensional or three-dimensional representation of an at least approximately specular reflected target, such as bone. In an example, echo information can be obtained from spatially-overlapping tissue regions, such as using one or more of an array of ultrasonic transducers, or mechanically-scanning one or more ultrasonic transducers. In an example, one or more of a deformable housing or a deformable coupling pad can be used, such as to couple ultrasonic energy between one or more transducers and a tissue region.

Abstract: A piezoelectric device includes a base, a vibration film, and a piezoelectric element. The base of the piezoelectric device has at least one opening. The opening is closed by the vibration film. The piezoelectric element is located on the vibration film. The vibration film includes a first layer that is has lower water permeability than silicon oxide and a second layer that is in close contact with the first layer and that has a larger toughness value than the first layer.

Abstract: Provided is an ultrasound transducer for irradiating a subject with ultrasound and receiving an ultrasound echo reflected from the subject. The ultrasound transducer includes a plurality of piezoelectric elements configured to emit ultrasound according to input of an electric signal and convert ultrasound incident from outside into an electric signal, and a mask portion provided between the plurality of piezoelectric elements and a radiation surface of the ultrasound on the ultrasound transducer. The mask portion is configured to: mask any divided region among a plurality of divided regions obtained by dividing an elevation direction orthogonal to a plane parallel to a scanning direction of the ultrasound; reflect the ultrasound in a direction different from a propagation direction of the ultrasound on the masked division region; and allow the ultrasound to pass in the propagation direction in the plurality of divided regions except the masked divided region.

Abstract: An ultrasonic diagnostic imaging system is operated to acquire an ultrasound image of a region of the body containing suspect anatomy such as a suspected lesion. A body marker template (104, 106) of the region of the body is displayed on a touchscreen display of the imaging system. The operator records the location of the suspect anatomy by touching a corresponding point on the body marker template displayed on the touchscreen display. The mark (120 a, 120 b) on the template can be finely adjusted by one or more controls on the imaging system control panel. The body marker template can also record a graphic indicating (120 c) the orientation of the ultrasound probe relative to the body when the suspect anatomy was imaged. A report generator produces a report containing both the ultrasound image of the suspect anatomy and the body marker template with the indicated location of the suspect anatomy.

Abstract: A system for automatically determining a thickness of a wall of an artery of a subject includes an ECG monitoring device that captures an electrocardiogram (ECG) signal from the subject, and an ultrasound video imaging device, coupled to the ECG monitoring device, that receives the ECG signal from the ECG monitoring device, and captures a corresponding ultrasound video of the wall of the artery of the subject. The system produces a plurality of frames of video comprising the ultrasound video of the wall of the artery of the subject and an image of the ECG signal. A processor is configured to select a subset of the plurality of frames of the ultrasound video based on the image of the (ECG) signal, locate automatically a region of interest (ROI) in each frame of the subset of the plurality of frames of the video using a machine-based artificial neural network and measure automatically a thickness of the wall of the artery in each ROI using the machine-based artificial neural network.

Abstract: According to one embodiment, an ultrasonic diagnostic apparatus sets a desired period with reference to a predetermined time phase in each heartbeat of the object, sequentially executes ultrasonic scanning on a plurality of sub-volumes in a period including the diagnosis period to acquire sub-volume data corresponding to a plurality of time phases, controls acquisition timing of the sub-volume data from a time point elapsed from the predetermined time phase by a predetermined period of time while switching the sub-volume, generates composite sub-volume data or a full volume data constituted by a plurality of sub-volume data by performing combining processing of the sub-volume data acquired in the different diagnosis periods, detects at least one of a cyclic change of a heartbeat signal and a change in the number of sub-volume data acquired in the one diagnosis period and performs combining processing of sub-volume data based on a detection result.

Abstract: The present invention relates to a kit for taking biopsies, resections, excisions, and/or autopsies. Moreover, the present invention relates to methods of taking biopsies resections, excisions, and/or autopsies using the kit of the present invention. The kits and methods of the present invention allow for fewer errors, decreased turn around time and/or more rapid processing due to a cassette and specimen numbering system that is simplified and superior over that which has been previously disclosed in the prior art. The kit of the present invention comprises one or more tissue cassettes, and optionally one or more bottles of formalin and optionally, other components.

Abstract: A device for closing an aperture in a vessel wall comprising a covering member having a longitudinal axis and positionable inside the vessel against the internal opening of the aperture and a first spherical retainer positionable external of the vessel. The covering member has a dimension to prevent egress of fluid through the aperture.

Abstract: A surgical instrument includes a cannula and a member coupled to the cannula. The member includes a first locking element. The surgical instrument further includes a patient attachable ring having a second locking element configured to engage the first locking element to fix the cannula relative to the patient attachable ring. Systems and methods are disclosed.

Abstract: A lumbar spine fusion system includes a probe and a retractor blade. The probe includes a shaft, a pointed tip, and a collar. The pointed tip is configured to puncture tissue in a disk space of a disk and anchor the probe to the tissue. The collar is configured to act as a stop to control a distance through which the shaft of the probe traverses the tissue. The retractor blade includes an end portion and a slot. The slot is configured to receive at least a portion of the shaft of the probe. At least a portion of the end portion is configured to rest upon one or more of the disk and the collar when the retractor blade is mounted on the probe.

Abstract: A system and method for performing spine surgery, including a tissue distraction assembly. The tissue distraction assembly includes an initial dilator, a secondary dilator, a first expander, and a second expander. The tissue distraction assembly is provided with an overall generally oblong shape. The tissue distraction assembly provides for asymmetrical tissue distraction in a single direction.

Abstract: The present invention relates to a surgical anchor delivery system (10) including a delivery device (11) having a shaft (14) and a handle (13), an advancer (15) for advancing a surgical anchor (12) distally along the shaft (14); and a plurality of surgical anchors (12) loaded upon the shaft (14).

Abstract: A suture anchor assembly including a suture anchor that incorporates a harder distal tip with a softer proximal body. The tip and body of the suture anchor are connected via a threaded plug, which also serves to connect the suture anchor to an inserter.

Abstract: A method for knotlessly securing suture in a bone tunnel including securing a suture to a tissue to be fixated by a suture anchor; preloading a proximal threaded component of an anchor onto a drive shaft; preloading a distal component of the anchor onto an actuator shaft, passing the suture through an eyelet of the distal component of the anchor, inserting the distal component of the anchor and then the proximal component of the anchor into the bone hole; confirming the placement of the proximal component of the anchor relative to the distal component of the anchor by viewing an indicator on the driver handle; and pivoting a trigger device about a pivot axis to translate the actuator shaft to a second position to compress the suture at the distal end of the proximal anchor and to lock the distal anchor to the proximal anchor.

Abstract: The present invention relates to a suture which is firmly maintained and fixed to an operation site to stably sustain suturing or lifting effects for a long time. More specifically, the present invention provides a suture having a conic or pyramidal shape with a cut top, wherein a suture supporter comprising a communication hole penetrating the both ends is provided at one end. The suture support can have one or more portions which are cut vertically from a lower end at a lower end portion having a larger diameter between the both ends, or a part of the lower end can be removed so as to form one or more gaps formed from the end at a wall of the end portion.

Abstract: An instrument for delivering a suture transfascially may include a handle, a shaft extending from the handle, and at least one needle that is moveable to an extended position beyond the end of the shaft. A suture may be delivered transfascially with the instrument. The instrument may include a suture catch associated with each needle for retaining and releasing a suture segment. A shield may be provided to shield the sharp end of each needle when it is moved to the extended position. A method of delivering a transfascial suture may include inserting an instrument into an abdominal cavity and deploying, from within the abdominal cavity, each needle through a soft tissue repair patch and then through at least part of the abdominal wall. A suture or suture segment may be advanced across the fascia with the at least one needle.

Abstract: A knotless self-cinching suture construct device includes a shuttling suture, a continuous loop and a self-cinching suture member. The shuttling suture is configured for insertion into a passage hole in injured soft tissue, such as a torn or damaged meniscus in the knee. The shuttling suture and continuous loop are passed entirely through the passage hole in the tissue, and the self-cinching suture member is inserted through the continuous loop to form a hitch using the continuous loop around the tissue. The self-cinching suture member is then pulled tight, allowing a first strand to slide through both the hitched continuous loop and a self-cinching sleeve on the suture member. When tension is applied, the sleeve tightens around the strand much like a finger trap, preventing inadvertent release of the applied suture tension. The suture construct is configured for use through a transosseous tunnel with a suture button in some embodiments.

Abstract: An apparatus and method for joining members together using a self-drilling screw apparatus or stapling apparatus are disclosed. The screw apparatus includes a shell and first and second first screw members having tapered ends and threaded bodies that are disposed within the shell. A drive mechanism rotatably drives the first and second screw members from the shell in opposite directions and causes the screw members to embed themselves in the members to be joined. The screw apparatus can be used to join members such as bones, portions of the spinal column, vertebral bodies, wood, building materials, metals, masonry, or plastics. The stapling apparatus includes first and second lever arms rotatably joined together at a fulcrum, and the lever arms rotate in opposite directions. First and second cartridges are disposed at the ends of the lever arms. Each cartridge is capable of holding a staple including a bracket, a nail member and an alignment slot.

Abstract: A cartridge of a surgical instrument includes a housing, a lead screw mounted for rotation in the housing, a drive member operatively coupled with the lead screw, and a knife member. The knife member is driven distally by the drive member and is configured to cut when moved distally. During an initial distal movement of the drive member, the knife member is coupled with the housing to restrain the knife member from moving distally. Subsequent to the initial distal movement of the drive member, the drive member drives the knife member toward the distal end.

Abstract: A motor driven surgical instrument that includes a surgical end effector configured to perform at least one surgical procedure in response to firing motions applied thereto from a firing system. The surgical instrument further includes an articulation system that is configured to facilitate articulation of the end effector relative to an elongated tool axis. The instrument further includes a coupler assembly configured to enable the motor to selectively power the firing system and the articulation system.

Abstract: A jaw member for use on a surgical stapling instrument includes a cartridge assembly and a cartridge housing each having an arcuate configuration. The cartridge assembly includes a surface configured to engage tissue and a plurality of rows of fastener retaining slots extending along a length of the cartridge assembly. The cartridge housing defines a channel configured for receipt of the cartridge assembly. The cartridge housing includes a base portion and a plurality of tabs. The base portion has a concave inner edge and a convex outer edge. The tabs extend from the concave inner edge and the convex outer edge. The tabs are spaced from one another along a length of the cartridge housing.

Abstract: A surgical stapling apparatus is disclosed which comprises cartridge body and a layer. The layer is implantable against tissue by staples deployed from the cartridge body and deformed by an anvil. The cartridge and the layer comprise co-operating features which reduce relative movement between the cartridge and the layer. Such co-operating features can also releasably retain the layer to the cartridge body. The layer can comprise buttress material and/or a tissue thickness compensator, for example.

Abstract: An improved surgical apparatus actuator includes a nail bin assembly (1002), a nail anvil assembly (1001) connecting with the nail bin assembly (1002), and a drive assembly (1003) controlling the nail bin assembly (1002) and the nail anvil assembly (1001) to convert between opening and closing conditions. The nail anvil assembly (1001) includes a nail anvil plate (103) and a nail anvil seat (102), wherein the nail anvil plate (103) is provided on an inner side (1022) of the nail anvil seat (102), the nail anvil seat (102) has the structure, material and processing technology capable of providing high anti-bending performance, the nail anvil plate (103) is cold-punched from a thinner stainless steel sheet. Therefore, the processing difficulty of the components is reduced, and meanwhile, the ability of the actuator chuck to resist bending deformation is improved.

Abstract: Devices and methods for applying sealants to surgical instruments. In one embodiment, a surgical device is described that can include at least one nozzle formed at a proximal end of the device that is configured to receive a sealant, as well as an applicator formed at a distal end of the device that is configured to deliver the sealant received by the at least one nozzle. The applicator can be configured to interface with at least one of a first and second jaw of a surgical stapler such that the sealant delivered from the applicator can be deposited into a plurality of openings formed in the surgical stapler.