Abstract: A device and system for supporting a patient or an object in an examination is provided. The supporting system may include a portion for supporting the body of a patient and/or a head supporting device. The portion for supporting the body may move in one or more directions. The head supporting device may be adjust to meet requirements of imaging when the patient or the object is supine or prone.

Abstract: An imaging system (1400) includes a first and a second focal spot (1410I and 1410N), a first pre-patient radiation beam filter (1416) disposed between the first focal spot and the examination region and having a first profile and a second pre-patient radiation beam filter (1416N) disposed between the second focal spot and the examination region and having a second profile, and a source controller (1412) that controls an operation of the focal spots by modulating the operation during a scan based on at least one of an angular position of focal spots, a shape of a region of interest of subject or object being scanned, or based on a change in size between two adjacent regions of the subject or object being scanned.

Abstract: A biplanar X-ray imaging device includes a second C-shaped arm and a first C-shaped arm which can be slidably disposed on the second C-shaped arm; a first X-ray generation device and a first image receiving device are disposed on the first C-shaped arm, thus constituting the first imaging device; a second X-ray generation device and a second image receiving device are disposed on the second C-shaped arm, thus constituting the second imaging device; the first C-shaped arm and the second C-shaped arm share the same rotating axis. For the biplanar X-ray imaging device, when the first C-shaped arm slides along the second C-shaped arm, different angles are formed between the first imaging device and the second imaging device; the first C-shaped arm and the second C-shaped arm share the same rotating axis, which ensures that the first imaging device and the second imaging device share the same rotating axis.

Abstract: According to one embodiment, an X-ray diagnostic system is used with an operation apparatus for operating, from a position separated from an object, a device inserted inside the object, and includes an imaging apparatus, an designation receiving circuit, a first display, and a second display. The imaging apparatus performs X-ray imaging of the object. The designation receiving circuit receives designation of a position on medical data from a first user who operates the device. The first display is disposed at a position visible from the first user, and displays a first image according to the designation of the position. The second display is disposed at a position visible from a second user who performs positioning of the imaging apparatus, and displays a second image different from the first image according to the designation of the position.

Abstract: A method is disclosed for recording medical images of the human body or that of an animal. The method includes scanning for acquiring data and signaling the start and/or end of a manual administration of a contrast medium in temporal relation to the scan for acquiring data.

Abstract: According to one embodiment, an X-ray diagnostic apparatus includes an imaging apparatus, processing circuitry and permission input circuitry. The imaging apparatus includes an imaging system performing X-ray imaging of an object, and a bed on which the object is placed. The processing circuitry accepts an instruction to cause the imaging apparatus to perform a operation, and notifies a content of the operation relating to the accepted instruction to a first user. The permission input circuitry accepts information indicating permission of the operation from the first user who has confirmed the content of the operation. The processing circuitry causes the imaging apparatus to perform the operation to more severely restrict the operation compared with after acceptance of information indicating permission of the operation by the permission input circuitry, until the acceptance of information indicating permission of the operation by the permission input circuitry.

Abstract: According to one embodiment, a nuclear medicine diagnostic apparatus includes a counting unit, a region of interest setting unit, a normalization unit, and an image generation unit. The counting unit counts radiation emitted from radioisotopes in an imaging region of an object. The ROI setting unit sets a region of interest (ROI) in the imaging region. The normalization unit determines association between count values and pixel values of display pixels for the ROI in accordance with a distribution of the count values of the display pixels corresponding to the ROI. The image generation unit generates an image of the ROI based on the association between the count values and the pixel values for the ROI.

Abstract: An imaging condition setting unit sets imaging conditions for a pre-contrast enhancement scan, a monitoring scan, and a post-contrast enhancement scan. A ROI setting unit sets a region of interest for the monitoring scan in a reference image generated by a reference image scan executed before the pre-contrast enhancement scan, the monitoring scan, and the post-contrast enhancement scan. The scan control unit controls an X-ray generation unit and an X-ray detection unit to sequentially execute, based on the imaging conditions, the pre-contrast enhancement scan, the monitoring scan, and the post-contrast enhancement scan.

Abstract: A receiving antenna for wirelessly receiving data between a stator of a computed tomography (CT) imaging modality and a rotor of the CT imaging modality is provided. The rotor rotates about a rotational axis. The receiving antenna includes a dielectric portion and a conductive portion coupled to the dielectric portion. A second surface of the conductive portion extends between a first end and a second end along a conductive axis that is substantially perpendicular to the rotational axis. The second surface of the conductive portion has a first length at a first length location along a first length axis that is substantially parallel to the conductive axis. The second surface of the conductive portion has a second length at a second length location along a second length axis that is substantially parallel to the conductive axis. The first length is different than the second length.

Abstract: The present invention provides an X-ray detection device and an apparatus and method for calibrating an X-ray detector, the method for calibrating an X-ray detector comprising: retrieving a calibration parameter stored in the X-ray detector relative to the X-ray detector; and calibrating the X-ray detector according to the calibration parameter.

Abstract: An ultrasound imaging system includes a scanning assembly, a three-dimensional (3D) image acquisition device, and a controller. The scanning assembly is configured to receive a hand or foot and includes a transducer array and an acoustic coupling fluid. The 3D image acquisition device is configured for obtaining a 3D image of the hand or foot. The controller is configured for automatically adjusting direction or orientation of the transducer array with respect to the hand or foot based on the 3D image of the hand or foot.

Abstract: A system for providing navigational guidance to a sonographer acquiring images is disclosed. The system may providehaptic feedback to the sonographer. The haptic feedback may be provided through an ultrasonic probe or a separate device. Haptic feedback may include vibrations or other sensations provided to the sonographer. The system may analyze acquired images and determine the location of acquisition and compare it to a desired image and a location for obtaining the desired image. The system may calculate the location for obtaining the desired image based, at least in part, on the acquired image. The system may then provide the haptic feedback to guide the sonographer to move the ultrasonic probe to the location to acquire the desired image.

Abstract: An information acquisition apparatus according to the present invention includes a container configured to store a deformable acoustic matching member, a receiving unit configured to receive an acoustic wave generated from an object and output a signal, and a processing unit configured to acquire object information based on the signal. The processing unit acquires sound speed information about the object, acquires sound speed information about the acoustic matching member, acquires positional information about the acoustic matching member, acquires propagation time information about the acoustic wave between an interesting position of the object and the receiving unit using the positional information, the sound speed information about the object, and the sound speed information about the acoustic matching member, and acquires the object information about the interesting position using the signal and the propagation time information.

Abstract: An imaging probe is disclosed for diagnosis, which includes an imaging core having a drive shaft internally provided with an optical fiber and a signal line. The imaging probe for diagnosis includes an optical transceiver that is disposed in one end of the optical fiber, and an ultrasound transceiver that is joined to the signal line. The optical transceiver is arranged on a distal side of the imaging core from the ultrasound transceiver. An emitting direction of an ultrasound wave emitted from the ultrasound transceiver and an emitting direction of light emitted from the optical transceiver are substantially parallel to each other, and are directions, which further tilt to a proximal end of the drive shaft than a direction orthogonal to the drive shaft.

Abstract: The present invention concerns a method for obtaining a functional parameter of a muscle having a part, the method comprising the steps of: a) applying ultrasound waves to the muscle, b) collecting the ultrasound waves retrodiffused by the muscle at a plurality of times, to obtain collected ultrasound waves, c) determining a first plurality of values representative of stiffness values of one part at a first plurality of times by using the collected ultrasound waves, d) determining a second plurality of values representative of deformation values of said part at a second plurality of times by using the collected ultrasound waves, and e) deducing at least one functional parameter based on the first plurality of values and the second plurality of values. The invention also concerns a corresponding device.

Abstract: An ultrasound imaging apparatus (20) is disclosed, comprising a data interface (30) configured to receive a plurality of different ultrasound data sets (26, 28) resulting from an ultrasound scan of an object (18) in different viewing directions. The ultrasound imaging apparatus further comprises a segmentation unit (32) for segmenting anatomical structures of the object in the different ultrasound data sets and for providing segmentation data of the anatomical structures, and a reference determining unit (34) for determining a spatial reference (48, 50, 52, 54) for the different ultrasound data sets on the basis of the segmentation data. A confidence determining unit (40) is included for determining confidence values (56) for different regions of the received ultrasound data on the basis of the spatial reference.

Abstract: Systems and methods for relaying electrical signals representing acoustic response of a volume of tissue to light and ultrasound stimulation. In an embodiment, a plurality of ultrasound transducers receive acoustic energy from the volume and generate electrical energy, which is transmitted via an electrical path to a relay system. The ultrasound transducers are operated at a wide band frequency of at least 1 MHz to 5 MHz to receive acoustic energy from the volume of tissue responsive to light stimulation and at a narrower band frequency to receive acoustic energy from the volume of tissue responsive to acoustic stimulation. The relay system relays the electrical signals to an optoacoustic system or an ultrasound instrument for further processing depending on whether the electrical signals resulted from ultrasound or light stimulation. In an embodiment, optoacoustic, ultrasound, or other images are generated from the electrical signals and may be coregistered, overlayed, or displayed.

Abstract: A tissue handling system includes a biopsy device configured to deliver at least one tissue sample to a location outside the body of a patient. A tissue storage container is separate from the biopsy device. A tissue collecting device is configured to releasably engage the biopsy device to receive the at least one tissue sample from the biopsy device. The tissue collecting device is configured to be disengaged from the biopsy device and engaged with the tissue storage container to deliver the at least one tissue sample to the tissue storage container.

Abstract: Systems and methods directed to sampling endothelial cells within a pulmonary vasculature are provided. The system and method may include a cell sampling device having an elongated sheath extending from a proximal end to a distal end of the cell sampling device and defining an access lumen. An endovascular brush includes brush elements coupled to a shaft. The endovascular brush is dimensioned to be received in the access lumen of the elongated sheath. An actuation control is coupled to the shaft of the endovascular brush to axially translate the endovascular brush between a retracted position and an expanded position. Upon translation of the endovascular brush from the retracted position to the expanded position, the brush elements moves from within the access lumen to the pulmonary vasculature to obtain endothelial cells from a target artery of the pulmonary vasculature.

Abstract: The invention relates to an automatic device for the insertion of a stylet and cannula to a predefined depth ? within a bone, said depth ? being irrespective of the thickness of the tissue above the bone, which comprises: (a) a trigger unit for activating the device; (b) a barrel; (c) a probe unit within said barrel which is driven by a secondary spring, said probe unit comprises one or more probing needles at a distal end, and an anvil at a proximal end for defining an end of movement location for a hammer unit; (d) a hammer unit which is driven by a main spring, said hammer unit comprises a stylet at its distal end, a core at its proximal end, and a piston in between said core and stylet, wherein said stylet is inserted to within a cannula, and wherein when said hammer unit is positioned at said end of movement location, a tip of the stylet which is longer than said one or more probing needles is located a distance ? farther to the distal direction from the respective ends of said probing needles; and (e) o

Abstract: A biopsy device includes an elongate member and a tissue anchor. The elongate member has a lumen and a sample receiving notch. The sample receiving notch has a proximal end wall, a distal end wall, and a floor between the proximal end wall and the distal end wall. The proximal end wall has a vacuum hole in fluid communication with the lumen. The tissue anchor has a plurality of cantilever portions. Each cantilever portion of the plurality of cantilever portions has a curved end, with a tip of the curved end configured to extend toward the floor of the sample receiving notch.

Abstract: The provided technologies provide an implant closure device having a mesh layer formed on a flexible substrate, collectively forming a sealable member, that improves a seal formed over an aperture in a body lumen. The mesh facilitates a faster and more secure adherence of the sealable member to the surrounding edges at the puncture site. Furthermore, the provided technology may promote platelet-capture and encourage localized platelet aggregation at the exposed collagen in the wound edges on the mesh layer. The platelet impregnated mesh layer can facilitate cellular adhesion, enabling the sealable member that is local to the wound opening to act, in essence, as a “biological glue.

Abstract: A suture grasping and passing device having a handle with an elongate tubular needle defining a lumen therein and extending from the distal end of the handle and having a pointed forward distal tip for puncturing soft tissue. A lateral radially open suture capture notch is provided in the tubular needle adjacent the pointed distal tip and defines a mouth open to the needle lumen. The notch mouth is contoured to receive a suture therein transversely across the mouth and an elongate gate member is slidably received for axial movement within the lumen whereby the gate member may be advanced in a forward direction to entirely close off an outer radial apex portion of the suture capture mouth to capture a suture under the gate member within the mouth of the notch.

Abstract: Described herein are methods and apparatuses for use in repair of a patient's tissue by connecting the tissue to the bone using a transosteal tunnel and anchor configured to pass through the transosteal tunnel. In particular, described herein are methods of repairing an anterior cruciate ligament (ACL) and torn meniscal root. These anchoring apparatuses and method of using them are particularly well suited for use with the low-profile suture passers described herein, since these suture passers may allow access to previously inaccessible regions of the knee (or other body regions).

Abstract: A suture tape construct having a first section formed from a fibrous filament that extends from a first end to a second end and has a pair of a one-way protrusions extending therefrom. An anchor is positioned along the suture construct and, when the construct is deployed, is captured between the protrusions. The anchor may be a second section formed from braided suture material that is woven about the first section. The braided suture material can be deployed to form an all suture anchor while protrusions extending from the suture anchor proximately to the location of the deployed suture anchor prevent movement of the second section relative to the first section, thus forming a non-sliding suture tape anchored by the deployed braided material. The anchor may be a threaded anchor having an eyelet that is captured between the protrusions.

Abstract: A surgical device includes a first fastener having a planar profile, a second fastener having a concave surface, and a suture that can be manipulated to change a distance between the first and second fasteners. The second fastener has a curvature that substantially matches the curvature of a top surface of a clavicle bone in a direction perpendicular to a long axis of the clavicle bone. A method of treating an acromioclavicular joint injury includes forming axially aligned passages through a patient's clavicle and coracoid process, passing a fastener having a concave surface through the passages, positioning the concave surface of the fastener against a top surface of the patient's clavicle with a long axis of the fastener extending perpendicular to a long axis of the clavicle, positioning a fastener having a planar profile below the patient's coracoid process, and adjusting a suture that couples the fasteners.

Abstract: An endoscopic surgical stapler for applying a suture to tissue including an elongated tubular member, a first jaw positioned at the distal end portion of the tubular member and having a longitudinal axis, and a second jaw disposed in substantially parallel relation to the first jaw at the distal end portion of the tubular member. The second jaw is movable in a direction substantially perpendicular to its longitudinal axis toward the first jaw, while maintaining the substantially parallel relation between the first and second jaws. A stapling assembly is disposed in each of the first and second jaws and configured to apply surgical staples to the tissue such that a suture, in combination with the surgical staples, forms a purse string with the tissue when the surgical stapler is activated.

Abstract: A suture anchor includes a material having thermoplastic properties and is fixated in a hard tissue opening by liquefying at least part of this material and letting it penetrate into walls of the hard tissue opening. During the named fixation and preferably towards the end of it, the suture being held in a distal suture conduit is locked relative to the hard tissue by being clamped between the suture anchor and the wall of the hard tissue opening or by being clamped or braked through collapse of the suture conduit.

Abstract: The present invention relates to a thread implantation rod and relates to a needle for thread-embedding therapy having a tubular shape for allowing a suture to be inserted and moved therein, wherein the end is rounded and blocked and also has a sharp shape so as to prevent the skin, muscle and blood vessels from being torn during an operation, thereby preventing damage to subcutaneous tissue.

Abstract: An instrument used for brachytherapy delivery in the treatment of cancer by radiation therapy including a handle having first and second handle actuators; an end effector; and an instrument shaft that connects the handle with the end effector. The end effector has first and second adjacent disposed staple cartridges that each retain a set of staples. The first mechanism is for holding standard staples in a first array, and dispensing the standard staples under control of the corresponding first handle actuator. The second mechanism is for holding radioactive source staples in a second array, and dispensing said radioactive source staples under control of the corresponding second handle actuator. The actuating device is removably attachable to an actuator arm on a proximal end. A staple applicator cartridge holder is attached to the actuator arm on a distal end. The staple applicator cartridge is mountable in the holder and having a plurality of slots for mounting of radioactive source staples therein.

Abstract: A chip assembly for use in a surgical stapler is provided. The chip assembly includes a housing assembly and a plug assembly. The housing assembly includes a base member, seal member, and a circuit board assembly. The base member defines a cavity for receipt of the circuit board assembly and the seal member is configured to be received about an open end of the base member. The plug assembly is configured to selectively engage the open end of the base member. The plug assembly includes a plug member and first and second contact members extending from the plug member. The first and second contact members are configured to be received within the cavity defined by the base member and engage the circuit board assembly when the plug assembly engages the housing assembly.

Abstract: A method and apparatus for coupling a soft tissue implant into a locking cavity formed within a bone is disclosed. The apparatus includes a member to pull the soft tissue implant into a femoral tunnel. The member includes a suture having first and second ends which are passed through first and second openings associated with the longitudinal passage to form a pair of loops. A collapsible tube is positioned about the suture. Application of tension onto the suture construction causes retraction of the soft tissue implant into the femoral tunnel and the collapse of the tube to form an anchor.

Abstract: An end effector for use with a surgical instrument having a first cartridge assembly configured to deploy a first set of fasteners and a second cartridge assembly disposed distally of the first cartridge assembly. The second cartridge assembly is configured to move between an open position and an approximated position relative to clamp tissue. A central rod extends between the first cartridge assembly and the second cartridge assembly.

Abstract: A surgical stapler comprising a handle assembly, an elongated body portion extending distally from the handle assembly, and a head portion disposed adjacent a distal portion of the elongated body portion and including an anvil assembly and a shell assembly. The anvil assembly is movable in relation to the shell assembly between spaced and approximated positions. The anvil assembly has an anvil head and a plurality of projections extending proximally of the anvil head, the projections engageable with a portion of the shell assembly.

Abstract: A surgical device comprising a handle housing, an adapter, an elongated portion, an end effector, a first drive element, and a second drive element is disclosed. The adapter includes a first drive assembly configured to mechanically engage a portion of a first actuation mechanism of the handle housing. The elongated portion is configured to extend distally from the adapter. The first drive element is disposed in mechanical cooperation with the first drive assembly. The second drive element is disposed in mechanical cooperation with the first drive assembly. Rotation of the first drive assembly in a first direction about the longitudinal axis causes distal translation of the first drive element. Rotation of the first drive assembly in a second direction about the longitudinal axis causes distal translation of the second drive element. The first direction is opposite from the second direction.

Abstract: A system for occluding a physical anomaly. One embodiment comprises a shape memory material body wherein the shape memory material body fits within the physical anomaly occluding the physical anomaly. The shape memory material body has a primary shape for occluding the physical anomaly and a secondary shape for being positioned in the physical anomaly.

Abstract: An occlusive device includes a frame element having a distal end and a proximal end, and a delivery configuration and a deployed configuration. The occlusive device also includes an occlusive face having a peripheral edge, where the occlusive face positioned toward the proximal end of the frame element. The occlusive device also includes at least one anchor positioned at the peripheral edge of the occlusive face, where the at least one anchor extends at an acute angle to the peripheral edge of the occlusive face.

Abstract: A method of forming a bone cutting block includes: forming a plurality of saw slot plates and two side plates, the plurality of saw slot plates each including a plurality of ends opposing one another, each of the plurality of ends including a locating feature, the side plates including a plurality of locating features; and supporting the plurality of saw slot plates using the side plates, each locating feature of the plurality of saw slot plates being connected with a respective one of the plurality of locating features of the side plates and the side plates thereby opposing one another, the plurality of saw slot plates defining at least one slot therebetween which is configured for receiving a bone saw blade therethrough to make a predefined cut in a bone.

Abstract: An orthopedic trauma drill is provided that includes an automatic measuring component to ensure that the proper drill depth is achieved for the length of the appropriate screw that is required. The drill may include a stationary sleeve over a drill bit which determines the distance that the drill bit has drilled through a bone, and may provide a real-time numerical readout of the distance measurement. The drill may also include torque sensor to determine the rotation of the drill in revolutions per minute during operation of the drill.

Abstract: The present disclosure relates to resection devices and methods. The resection device includes an outer tubular member; and an inner tubular member disposed within the outer tubular member, the inner tubular member including a burr having a body with flutes extending along a length of the body, the flutes including parabolic wave patterns located along surface edges of the flutes. In an embodiment, the parabolic wave patterns extend along entire lengths of the flutes. Other resection devices and methods are also disclosed.

Abstract: A method for performing a surgical procedure includes planning a resection of a bone of a patient. A volume of the bone is removed according to the planned resection using a surgical tool. As the bone is removed, data corresponding to a shape and volume of the removed bone is tracked with a computer system operatively coupled to the surgical tool. A prosthesis is implanted onto the bone of the patient based on the tracked data corresponding to the shape of the removed bone.

Abstract: A limited use acetabular reamer can be used to perform selected procedures. The limited use reamer can be formed of low cost materials and be assembled in a limited number of steps. For example, a cutting portion can be formed or a metal and a body portion can be formed of a polymer.

Abstract: Systems, methods, and devices provide for a bone centering drill guide. The bone centering drill guide may include a clamping mechanism which clamps to a bone in a pivotable fashion. The proximal end of the clamping mechanism includes a handle portion having a first arm and a second arm which is configured to allow a user to grip the device and exert force which urges the first and second arms toward each other. The distal end includes a clamping portion having first and second arms which are urged into a closed configuration when closing force is provided to the handle portion. The proximal end may further include a locking mechanism which locks the clamping device in a clamped configuration. The bone centering drill guide may further include a guide slot disposed on the distal end above the clamping arms, the slot configured to remain centered between the first and second clamping arms.

Abstract: The present disclosure in one aspect provides an adjustable depth drill guide comprising a trigger assembly further comprising a trigger and a primary actuating element and a telescopic rotational assembly which abuts the primary actuating element and further comprises an intermediate actuating element. The drill guide described herein allows a surgeon to adjust the depth of the drill guide using only one hand while in-situ.

Abstract: Systems and methods for preparing a bone for a surgical procedure are provided. In general, the described techniques use a surgical guide device including a cannula having first and second parallel elongate channels adjacent to one another, and first and second elongate sleeves configured to be removably and replaceably received in the first and second channels, respectively. The first sleeve has a plurality of openings formed therein, each being in communication with a respective wire-receiving lumen extending through the first sleeve. Each of the openings defines a different offset distance between the wire-receiving lumen in communication with that opening and a wire-receiving lumen extending through the second sleeve. The surgical device can be manipulated so as to define positions of first and second openings in a bone, such as a glenoid or other bone, to receive bone screws or other elements for attaching a bone graft to the bone.

Abstract: A system for removal of blood or thrombus includes an aspiration catheter having an elongate shaft including an aspiration lumen having proximal end configured to couple to a vacuum source, and a distal end having an orifice, an elongate member configured for placement through the aspiration lumen and having a distal portion including a disruption element configured to disrupt thrombus within the aspiration lumen, and a monitoring device configured for removable connection in between the aspiration catheter and the vacuum source, and including a housing, a pressure sensor in fluid communication with an interior of the housing, a measurement device coupled to the pressure sensor and configured for measuring deviations in fluid pressure, and a communication device coupled to the measurement device and configured to generate an alert signal when a deviation in fluid pressure measured by the measurement device exceeds a pre-set threshold.

Abstract: Vascular treatment and methods include a plurality of self-expanding bulbs and a hypotube including interspersed patterns of longitudinally spaced rows of kerfs. Joints between woven structures and hypotubes include solder. Woven structures include patterns of radiopaque filaments measurable under x-ray. Structures are heat treated to include at least shapes at different temperatures. A catheter includes a hypotube including interspersed patterns of longitudinally spaced rows of kerfs. Heat treating systems include a detachable flange. Laser cutting systems include a fluid flow system.

Abstract: In a liquid ejection control apparatus, an operation unit includes adjustment levers for changing a rising frequency, voltage amplitude, and the like of a drive voltage waveform applied to a piezoelectric element. In a control unit, a rising frequency setting section sets a rising frequency in response to an input operation on a rising frequency adjustment lever so as to make constant a change amount regarding momentum related to a pulsed liquid jet ejected from a liquid ejection device and the change amount per unit operation level for the rising frequency adjustment lever in a state in which voltage amplitude of the drive voltage waveform is set to a predetermined value.

Abstract: A surgical scalpel is presented which combines the attributes of cost-effectiveness in design while being ambidextrous and autoclavable. The design of the device affords left handed or right handed medical personnel with the feel, weight and balance of the original metal unguarded scalpel, while maintaining safety through the shielding of the blade during non-use and the ability to dispose of the blade in a safe controlled manner without having to place ones hands near the unguarded sharp. Surgeons of either dexterity are able to learn and operate using similar techniques and instruments heretofore not available to them. No longer must a left handed surgeon be forced into the right handed world to perform surgery. The device is designed to use existing styles of blades currently available without needing costly inventories of specially created blades for the multitude of other such devices on the market.

Abstract: The present disclosure relates to the field of endoscopy. Specifically, the present disclosure relates to systems and methods for en bloc resection of malignant and pre-malignant lesions and/or tumors within the gastrointestinal (GI) tract. More specifically, the present disclosure relates to systems and methods for delivering an expandable scaffold between tissue layers (e.g., between the muscularis and submucosa layers) to elevate and stabilize the lesion or tumor for fast and efficient resection.