Abstract: The present invention provides systems and methods for stabilizing or adjusting the position of at least one spinal motion segment.

Abstract: A rasp tool for preparing an implantation site includes a first arm, a second arm, a first wing, and a second wing. The first arm and the second arm are pivotally connected to one another. The first wing extends from a distal end of the first arm and includes a sharp tip positioned at a distal end of the first wing and configured to ease insertion into the implantation site, and a cutout defined along a first side of the first wing. The second wing extends from a distal end of the second arm. The first wing and the second wing are configured to move between a closed position and an open position by pivoting the first arm and the second arm, and the second wing is received at least partially within the cutout when the first wing and the second wing are in the closed position.

Abstract: A system for securing a flexible member to a vertebra includes a flexible member, a fixation member, and an inserter. The flexible member includes two ends. The fixation member includes a head and a shank that defines a longitudinal axis of the fixation member. The head defines a slot that passes through the head orthogonal to the longitudinal axis. The slot receives a portion of the flexible member. The inserter includes a handle and a tubular member that has proximal and distal end portion. The proximal end portion is attached to the handle and the distal end portion extends from the handle. The tubular member defines a passage between the proximal and distal end portions. The distal end portion includes a couple for receiving the head of the fixation member with the portion of the flexible member received in the slot of the flexible member.

Abstract: Certain embodiments of the invention provide plates for treating periarticular fractures or other non-full body weight bearing applications that combine polyaxial fixation with a low profile and enhanced contouring that more closely conforms to bone. Such plates can be designed to achieve buttressing effect and/or to be used in a reinforcement mode. Other features can be combined with these. Such plates can be created for use on bone sites such as on a tibia, fibula, metatarsal, calcaneous, other foot bone, humerus, radius, ulna, spinal, maxillofacial, as well as sites on other bones.

Abstract: An implant for bone fixation is presented. The implant comprises an elongated member configured to be wound around bone parts that are to be fixed. Further, an engagement feature is provided that is coupled to the elongated member and configured to engage a portion of the elongated member so as to secure the implant in a loop around the bone parts. A fastening member is arranged between and coupled to the elongated member and the engagement member. The fastening member comprises at least one opening for receiving a bone fastener. In one variant, at least one visual indicator indicating a region of the fastening member to be severed in order to detach the implant is provided. In another variant, at least one of the engagement member and the elongated member are coupled to the fastening member by injection molding.

Abstract: A surgical staple (714) for inserting into one or more bone parts (10, 12) comprises a plate (718), a first screw (748) and a second screw (748). The plate (718) includes a first end (768F), an opposed second end (768S), a first aperture (742) that is positioned near the first end (768F), and a second aperture (742) that is positioned near the second end (768S). Additionally, the plate (718) is curved along a length of the plate (718) from the first end (768F) to the second end (768S). The first screw (748) extends through the first aperture (742). The second screw (748) extends through the second aperture (742). Further, the first screw (748) and the second screw (748) are angled toward one another when the surgical staple (714) is in a relaxed configuration.

Abstract: Techniques disclosed herein include systems and methods for a bone screw and self-retaining driver. The system includes a mechanism that enables a bone screw to be rigidly attached to a screwdriver for manipulation and transfer of bone fragments and grafts to a fixation site, such as during surgery. The system includes a cannulated bone screw that has a drive connection that engages with a drive structures of a screwdriver. The bone screw also includes a structural connector that securely attaches to or receives an internal shaft or rod of the screwdriver. The internal shaft or rod of the screwdriver can rotate and slide independent of an outer shaft of screwdriver. Accordingly, the internal shaft of the screwdriver can rigidly connect with the bone screw enabling applied torque to the screwdriver to be transferred to the bone screw, without the bone screw falling off of the drive connection.

Abstract: This disclosure describes exemplary screw and intramedullary devices that are better able to bring bone fragments into close proximity with each other, generate a compressive load, and maintain that compressive load for a prolonged period of time while healing occurs. The devices are made of a shape memory material.

Abstract: The invention provides a surgical tool (1), e.g. a hand-held tool, for inserting surgical implants in a patient's body, the tool comprising: a main body (2) extending along a longitudinal axis (X-X?) between firstly a working end (3) and secondly a proximal end (4), the main body (2) also presenting an outside surface (5) connecting the working end (3) to the proximal end (4); and a guide cannula (14) arranged within the main body (2) and extending between a distal orifice (15) opening to the outside of said main body (2) at the working end (3), and a rear orifice (16); said surgical tool (1) being characterized in that said rear orifice (16) opens out to the outside surface (5) of said main body (2), and in that said main body (2) presents longitudinal splines (25, 27, 28) projecting from said main body (2) in respective planes extending. radially relative to the longitudinal axis (X-X?). Surgical instrumentation.

Abstract: A bone graft delivery system can include an elongate tube, a handle having a trigger, and a tip. The trigger is actuated to deliver bone graft material through the tube. The tip has one or more openings to deliver the bone graft material to a desired location and includes a surface suitable to act as a rasp for decorticating bone. A method for delivering bone graft material to a desired surgical location includes providing a bone graft delivery device, positioning the device adjacent the surgical location, decorticating bone, and delivering bone graft material to the surgical location.

Abstract: A device for dispensing biomaterial includes a handle configured to receive a syringe, the syringe including a biomaterial and a threaded plunger, and an engagement pin retained within the handle and slidable between a first position and a second position. The engagement pin is configured to engage the threaded plunger in the first position, the engagement pin is further configured to disengage from the threaded plunger in the second position.

Abstract: A cartridge for mixing and injecting bone cement includes a body including a cylindrical member, a first coupler and a second coupler at a first open end and a second open end of the cylindrical member, respectively, a first opening/closing member detachably coupled with the first coupler, a second opening/closing member detachably coupled with the second coupler, and a mixing ball in an internal space of the body. A bone cement mixing and transferring system includes the cartridge having powder and liquid components of bone cement inserted and mixing the powder and liquid components, an injection tube coupled with the cartridge after removing the first opening/closing member from the cartridge, and a cement gun mounted to a rear side of the second opening/closing member, the cement gun applying pressure for injecting bone cement mixed in the cartridge into an area to be treated via the injection tube.

Abstract: Disclosed are devices, systems and methods for improving the cleaning and/or sterilization of medical instruments and related tools, such as a cleanable ratcheting module that can be attached to various surgical instruments used during surgery, and then easily and efficiently cleaned. Cleaning of the tool is facilitated by various ports and/or openings in the device that allow for cleaning fluids, liquids and/or other gases to freely flow through interior aspects of the module.

Abstract: Cartilage and other tissues are treated by generating a plasma in an interior space of a probe and exposing the tissue to the plasma. The plasma is released through a gap in a working end of the probe.

Abstract: Surgery systems and methods for providing vibration feedback are disclosed. A surgery system includes an electrocautery tool, a current sensor, and an actuator. The current sensor is coupled to the electrocautery tool to sense a current through the electrocautery tool indicative of an electrocautery action being performed with the tool. The actuator is in communication with the current sensor and is configured to provide a vibration to an operator of the electrocautery tool when the current sensor senses the current through the electrocautery tool indicative of the electrocautery action. A surgical method includes sensing a current through an electrocautery tool indicative of an electrocautery action being performed with the tool, and actuating an actuator to provide a vibration to an operator of the electrocautery tool when the current sensor senses the current through the electrocautery tool indicative of the electrocautery action.

Abstract: An electrosurgical generator includes a radio frequency output stage, a sensor for sensing current, and an active lead. The radio frequency output stage is configured to output at least one radio frequency waveform. The sensor includes a current sensor coil including an outer coil including an opening therethrough and an inner coil coupled to and disposed within the outer coil. The active lead is coupled to the radio frequency output stage and passes through the current sensor coil opening. The current sensor coil is configured to output a first signal indicative of a current within the active lead.

Abstract: Methods for treating dyspnea with therapeutic renal neuromodulation and associated system and methods are disclosed herein. One aspect of the present technology, for example, is directed to methods that block, reduce, and/or inhibit renal sympathetic nerve activity to achieve a reduction in central sympathetic tone. Renal sympathetic nerve activity may be altered or modulated along the afferent and/or efferent pathway. The achieved reduction in central sympathetic tone may carry therapeutic benefits for patients with dyspnea.

Abstract: The present invention relates to the field of biomedical engineering and medical treatment of diseases and disorders. Methods, devices, and systems for in vivo treatment of cell proliferative disorders are provided. In embodiments, the methods comprise the delivery of high-frequency bursts of bipolar pulses to achieve the desired modality of cell death. More specifically, embodiments of the invention relate to a device and method for destroying aberrant cells, including tumor tissues, using high-frequency, bipolar electrical pulses having a burst width on the order of microseconds and duration of single polarity on the microsecond to nanosecond scale. In embodiments, the methods rely on conventional electroporation with adjuvant drugs or irreversible electroporation to cause cell death in treated tumors. The invention can be used to treat solid tumors, such as brain tumors.

Abstract: A system for controlling operation of a radiofrequency treatment device to apply radiofrequency energy to tissue to treat tissue to create lesions without ablating the tissue. The system includes a device having flexible outer tube, an expandable basket having a plurality of arms movable from a collapsed position to an expanded position, a plurality of electrodes movable from a retracted position to an extended position to extend through the openings in the arms, and an advancer slidably disposed within the outer tube to move the electrodes. An elongated spacer is positioned within the outer tube, the spacer having a central lumen to receive the advancer and to maintain a central position of the advancer.

Abstract: An electrosurgical instrument comprising a first arm carrying at least a first and optionally a second and third electrode, and a second arm opposing the first arm, the second arm carrying one of a nonconductor element or one or more conductive elements.

Abstract: Electrosurgical instruments and associated methods are disclosed herein. Embodiments of the electrosurgical instruments can include an elongate shaft that can articulate an end effector relative to the elongate shaft, with the end effector including opposed jaws and positioned at a distal end of the elongate shaft. In addition, electrosurgical instruments are provided that include a cutting feature or knife that is coupled to the end effector and can axially translate relative to the elongate shaft. Furthermore, the knife can be rotated relative to the elongate shaft, which can cause simultaneous rotation of the end effector. Electrosurgical instruments are also provided that include an end effector including opposed jaws that are configured to rotate relative to the elongate shaft and grasp objects (i.e., via opening and closing the opposed jaws). Electrical energy can also be passed through the electrosurgical instrument for performing electrosurgical procedures.

Abstract: An end effector assembly of a forceps includes a first jaw member and a second jaw member. The first jaw member and the second jaw member are selectively positionable relative to one another. At least one of the jaw members includes an electrically conductive tissue engaging surface configured to connect to an electrosurgical energy source, and at least one of the jaw members includes two blade channels defined therein and extending therealong and a feed in member selectively positioned between the two blade channels. The end effector further includes a cutting blade that is translatable such that selective positioning of the feed in member enables the cutting blade to selectively enter into at least one of the two blade channels.

Abstract: A coupler apparatus for coupling electrical signals between an actuator and an end effector is disclosed. The end effector is disposed at a distal end of an elongate articulated positioner and used to position the end effector for performing surgical operations. The articulated positioner has a central lumen and the apparatus includes an elongate body sized to be slidingly received within the central lumen of the articulated positioner, at least a portion of the body being operable to flex during movement of the articulated positioner. The apparatus also includes a plurality of electrical conductors extending through the body, and a plurality of proximal electrical contacts disposed at a proximal end of the body for removably connecting each of the electrical conductors to respective electrical signal lines at the actuator.

Abstract: A medical device includes a sheath extending from a proximal end to a distal end and having a lumen extending therethrough and an end-effector disposed at the distal end of the sheath including a first resection loop configured to resect tissue and a secondary tool including one of a second resection loop and a tissue-vaporizing structure mounted distally to the first resection loop.

Abstract: An electrosurgical apparatus having a HF power source providing HF energy for electrosurgery and a circuitry to control application of said HF energy to an electrode end used in electrosurgically operating on a patient is characterized in that said circuitry is adapted to apply in a dissecting mode said HF energy for dissecting to an electrode end automatically in the form of pulses such that the pulses automatically have a defined length. This device can be used for exploration of the bladder and en bloc radical removal of a large tumor using the active resection electrode loop of an optic resectoscope such that the bladder wall layers below the tumor base within the intact tissue margin are prepared using step-by-step coagulation and dissection of the tumor nutrient vessels and of the interlayer tissue fibers performed by impulsive turns-on of the electrosurgical apparatus in-use in the monopolar dissection mode.

Abstract: A method, including selecting a first maximum radiofrequency (RF) power to be delivered by an electrode within a range of 70 W-100 W, and selecting a second maximum RF power to be delivered by the electrode within a range of 20 W-60 W. The method also includes selecting an allowable force on the electrode within a range of 5 g-50 g, selecting a maximum allowable temperature, of tissue to be ablated, within a range of 55° C.-65° C., and selecting an irrigation rate for providing irrigation fluid to the electrode within a range of 8-45 ml/min. The method further includes performing an ablation of tissue using the selected values by initially using the first power, switching to the second power after a predefined time between 3 s and 6 s, and terminating the ablation after a total time for the ablation between 10 s and 20 s.

Abstract: A catheter and method for the treatment of a patient having atrial flutter or other arrhythmia comprises an elongated catheter body having an outer wall, proximal and distal ends, and at least one lumen extending therethrough. Further it has a distal tip section comprising a flexible tubing having a proximal end and a distal end and a plurality of lumens extending therethrough. The proximal end of the tip section is fixedly attached to the distal end of the catheter body. The tip section further comprises a nitinol tube having slots formed therein which causes the distal tip section to deflect using the same puller-wire action used to cause the deflectable catheter to deflect at a point proximal to the distal tip section.

Abstract: A photoablation device includes a laser source to propagate a focused laser beam with a beam waist, wherein a radius of the beam increases from the waist in a direction of propagation of the beam; an adjusting structure to adjust an intensity of the beam; a position detector to detect a position of the source in relation to the tissue; a positioning device to move the source in relation to the tissue; and a controller. The controller is to define a photoablation zone of the beam, wherein the zone ends in a cutting face located offset from the waist in the direction of propagation; adjust the intensity of the beam at the face of the zone using the adjusting structure; and move the beam towards the tissue by using the positioning device, wherein the position of the source detected by the position detector is evaluated.

Abstract: A cutting element for a cutting head for a device for cutting hair is disclosed. A laser beam is directed across a cutting zone, in the cutting head, substantially parallel to a user's skin. The laser beam has an effective cutting region in which the laser beam is of a sufficient intensity to cut hair entering said region. The cutting element has a guard adjacent to the cutting zone to contact a user's skin and space the laser beam there from. The guard has a non-planar shape in a direction extending across the cutting zone so that it substantially follows the contours of an edge of the effective cutting region of the laser beam to reduce any variation in the distance between the edge of the effective cutting region and the user's skin across the length of the cutting zone.

Abstract: Surgical tools having a two degree-of-freedom wrist, wrist articulation by linked tension members, mechanisms for transmitting torque through an angle, and minimally invasive surgical tools incorporating these features are disclosed. An elongate intermediate wrist member is pivotally coupled with a distal end of an instrument shaft so as to rotate about a first axis transverse to the shaft, and an end effector body is pivotally coupled with the intermediate member so as to rotate about a second axis that is transverse to the first axis. Linked tension members interact with attachment features to articulate the wrist. A torque-transmitting mechanism includes a coupling member, coupling pins, a drive shaft, and a driven shaft. The drive shaft is coupled with the driven shaft so as to control the relative orientations of the drive shaft, the coupling member, and the driven shaft.

Abstract: Devices and methods for performing a surgical step or surgical procedure with visual guidance using an optical head mounted display are disclosed.

Abstract: Various aspects of a surgical assistive device and method to provide assistance in neurosurgery are disclosed herein. The surgical assistive device includes circuitry that determines initial positional shift in the anatomical portion of a subject caused by an incision into a protective portion. A first depth value is estimated based on the plurality of stereo images that are captured from different specified positions of the surgical image capture device to capture views of the anatomical surface of the anatomical portion through the incision. A residual shift in a position of a surgical region of interest is determined with respect to the estimated first depth value. Surgical guidance information is generated to indicate a correct depth of the surgical region of interest in a surgical cavity, based on the determined residual shift. Display of the generated surgical guidance information is controlled on a display screen coupled to the surgical assistive device.

Abstract: The disclosure herein relate to systems, methods, and devices for developing patient-specific spinal treatments, operations, and procedures. In some embodiments, systems, methods, and devices described herein for developing patient-specific spinal treatments, operations, and procedures can comprise an iterative virtuous cycle. The iterative virtuous cycle can further comprise pre-operative, intra-operative, and post-operative techniques or processes. For example, the iterative virtuous cycle can comprise imaging analysis, case simulation, implant production, case support, data collection, machine learning, and/or predictive modeling. One or more techniques or processes of the iterative virtuous cycle can be repeated.

Abstract: Systems, methods and devices are provided for illuminating tissue with monochromatic or broadband light and imaging light that has been reflected back from the tissue. Imaging may be white-light imaging or hyperspectral imaging. The system can be a stand-alone hyperspectral imaging system, integrated as part of an external video scope, or as an auxiliary imaging module on an external videoscope. Various elements of a video scope that is particularly suited for minimally invasive surgery is first presented and then its configurations suitable for hyperspectral imaging are explained.

Abstract: The present teaching relates to surgical procedure assistance. In one example, a first set of positions of a plurality of sensors are obtained in an image captured prior to a surgical procedure. The plurality of sensors are coupled with a patient's body. One or more second sets of positions of the plurality of sensors are obtained based on information from a tracking device associated with the plurality of sensors. The one or more second sets of positions change in accordance with movement of the patient's body. One or more similarity measures are calculated between the first set of positions and each of the one or more second sets of positions of the plurality of sensors. A timing at which the surgical procedure initiates is determined based on the one or more similarity measures.

Abstract: At an imaging site an imaging device (14) generates an image of a subject (4) and an imaging light markers generation device (6) generates light markers at locations on a surface of the subject before an interventional procedure is performed. At an interventional site an interventional light markers generation device (17) generates light markers at the locations on the surface of the subject (4) and a localization device (25, 27) determines the position of a catheter during the interventional procedure. A position determination unit (29) then determines the position of the catheter within the pre-interventional image based on the position of the catheter determined by the localization device and provided spatial relations between the devices used for generating the image and the light markers and for localizing the catheter. This allows showing the position of the catheter within the pre-interventional image without necessarily using x-rays.

Abstract: There is described a method for tracking a patient in a coordinate system of a surgical tool using an optical waveguide modeling system having one multicore optical fiber with a portion attached to the surgical tool and a portion attached to the patient. The method generally includes receiving a patient model representing a shape and orientation of at least one of a limb and a bone of the patient, generating a waveguide model representing a shape and orientation of the multicore optical fiber as attached to the surgical tool and to the patient, and tracking the patient model in the coordinate system by registering the patient model in the coordinate system using the waveguide model and known spatial relationships relating to the surgical tool, the portion of the multicore optical fiber attached to the surgical tool, and the portion of the multicore optical fiber attached to the patient.

Abstract: A system and method for determining the spatial position and the shape of a surgical instrument (1) having a deformable body (2) by: providing an elasticity model of the surgical instrument (1); defining at least one parameter which influences the shape of the instrument (1); determining the spatial position and/or orientation of at least one tracking sensor (3) of the surgical instrument (1); determining the value of the at least one parameter; calculating the position and/or orientation of at least one part of the surgical instrument (1) with the aid of the elasticity model together with the determined value of the at least one parameter and the determined spatial position and/or orientation of the at least one tracking sensor (3).

Abstract: A method using a sheathed surgical apparatus includes equalizing a pressure differential between a surgical insufflation gas pressure and an initial pressure lower than the insufflation gas pressure. The insufflation gas pressure is external to a portion of a surgical apparatus upon which a sheath is disposed, and the initial pressure is within the surgical apparatus. The equalizing of the pressure differential occurs via permeation of insufflation gas through the sheath.

Abstract: The present embodiments relate to operator control in a master-slave robotic system, including, but not limited to, wherein an operator uses a master control input device to guide the position and orientation of a tool that is driven by the robotic system. Embodiments described herein provide devices and methods of increasing precision control for complex motions by, for example, decoupling operator control of rotational and translational movement.

Abstract: Described herein is a surgical instrument holder for use with a robotic surgical system, for example, during spinal surgery. In certain embodiments, the surgical instrument holder is an interface between the robotic arm and a surgical instrument used during surgery. This interface may hold the surgical instrument precisely, rigidly, and in a stable manner while permitting a surgeon to easily and quickly install or withdraw the instrument in case of emergency.

Abstract: A tool adapting device attaches to a robotic surgery arm, and receives a manual surgical instrument, and translates movement by the robotic surgery arm into multiple degrees of freedom of the manual surgical instrument, to interact with a tissue under surgery.

Abstract: A haptic glove configured to transmit haptic feedback to an operator of a surgical robot system may include: a plurality of vibrators on a first surface of the haptic glove, the plurality of vibrators configured to apply vibrations; at least one pressure sensor at a finger part of a second surface of the haptic glove opposite to the first surface, the at least one pressure sensor configured to sense grip force in the finger part; at least one sensation applier on the second surface, the at least one sensation applier configured to apply sensations including vibration or force to the finger part; and/or a controller configured to output the grip force sensed by the at least one pressure sensor, and configured to control the vibrations applied by the plurality of vibrators and the sensations applied by the at least one sensation applier.

Abstract: A method of manufacturing a glove that includes discrete elements and component systems, such as, but not limited to, lights, electrical cautery, suction, and irrigation, attached to the surgical glove. The gloves produced by this method can be used as surgical gloves or for other industrial applications. In a particular application, the method includes providing a former comprising a hand-shaped portion and a first surgical system comprising a first surgical instrument, and a first switch for controlling the first surgical system. The former includes a first depression for receiving the first surgical system. The first depression is adapted to produce an interference fit with at least a portion of the first surgical system. The first surgical system can be loaded into the first depression and a polymer coating can be applied over the loaded former to form a surgical glove.

Abstract: The invention relates to a lighting device (100), which is equipped for fastening to a surgical instrument (200) or, by means of adapter (90; 91), to a body part (92), in particular a finger of a surgeon or of an operating room assistant, in order to serve as a light source during a surgical operation, in particular within a body cavity or organ cavity of genuine or traumatic origin and in other body regions that are difficult to access. At least one pin (20) pointing outward from the wall of the housing (10) is arranged on the housing (10) of the lighting device (100) in a wall area (30) directed toward the surgical instrument in the fastening position, which pin has a light emitting opening (40) at the distal end of the pin and is designed for passing through an opening (220) of the surgical instrument or of the adapter (90; 91) and thus establishing a form-closed or force-closed connection to the opening. The pin (20) is preferably movable in order to achieve optimal illumination of the operation site.

Abstract: An ophthalmic illumination system includes a light source generating a source light beam and a beam splitter splitting the source light beam into first and second light beams. A first attenuator is located in a path of the first light beam and a second attenuator is located in the path of the second light beam, the first and second attenuators operable to change the intensities of the first and second light beams, respectively. A first optical fiber port is configured for connection to a first optical fiber for delivering the first light beam to a patient's eye and a second optical fiber port is configured for connection to a second optical fiber for delivering the second light beam to the patient's eye. A control unit is communicatively coupled to the first and second attenuators and is operable to adjust the attenuators to control the intensities of the light beams delivered to the patient's eye.

Abstract: Embodiments of claimed subject matter are directed to an illuminating surgical device comprising an array of illuminating elements and an array of louvers to direct light from the individual illuminating elements toward a surgical field.

Abstract: A grip (1), for a medical device (2), has an inner part (3), which has fastening features (6) for fastening to the medical device (2) and an outer part (4), which has a snap-in element (5), which can lockingly engage an snap opposing element (7) of the inner part (3) for the detachable fastening of the outer part (4) to the inner part (3) and at least partially overlaps the inner part (3) on surfaces not facing the medical device. An actuating element (8) is provided on the outer part (4), and is manually actuatable for unlocking detachment. The actuating element (8) is configured in one piece with the snap-in element (5) and the outer part (4) such that the actuating element (8) performs a movement with the snap-in element (5) in relation to the snap opposing element (7) during the unlocking.

Abstract: Embodiments include a fiducial deployment system with a handle configured for actuation of same. A fiducial may include one or more protuberances configured to engage one or more slots in a needle of the system. The needle may be configured to deliver a plurality of fiducials to a target location in serial fashion, one at a time. The handle includes an actuation mechanism with a recessible-toothed rack and actuation member(s) configured for incrementally or otherwise controlledly deploying one or more fiducials at a time by advancing a stylet through and/or retracting the body of a slotted needle in which fiducials are disposed with a fiducial protrusion extending into the needle slot, which needle slot also includes retaining structures that do not impede the needle lumen.

Abstract: A surgical instrument and a method for installing a RFID label on the surgical instrument are provided. The surgical instrument includes a surgical instrument body, a RFID label and an adhesive, the surgical instrument body and the RFID label are fixedly connection by the adhesive, the adhesive comprises a first adhesive and a second adhesive; the first adhesive is disposed between a bottom surface of the RFID label and a surface of the surgical instrument body, the other surfaces of the RFID label are covered by the second adhesive, the second adhesive also covers an intersection of the RFID label with the surgical instrument body; and the first adhesive and the second adhesive are different types of adhesives, and an adhesive intensity of the first adhesive is greater than an adhesive intensity of the second adhesive, and fluidity of the second adhesive is greater than fluidity of the first adhesive.