Abstract: An electrosurgical instrument for the treatment of tissue includes a longitudinal instrument shaft having a central axis, an end effector at the distal end of the shaft, the end effector including at least one element movable between a first and a second position. An actuator includes a handle which reciprocates movement between a first and second actuator position, and an actuation wire associated with the actuator for movement. Movement of the actuator causes the wire to move the element between its first and second positions, the wire running longitudinally of the shaft offset on one side from the central axis of the shaft. Compensation wire is associated with the actuator, the compensation wire running longitudinally of the shaft and being offset on the opposite side of the central axis of the shaft to that of the actuation wire.

Abstract: The present invention relates to a non-stick coated electrosurgical diathermy instrumentation, comprising: a handle portion; an isolation tube, connected to the handle portion by one end thereof; an instrument portion, connected to another end of the isolation tube, wherein an anti-sticking layer is formed on the surface of the instrument portion; and an electrode, connected to the handle portion and an external conductive member. In the present invention, the instrument portion is able to generate heat when the conductive member conducts electricity to the instrument portion.

Abstract: An interchangeable tip comprising: a stylet; a blade module including: an enclosure that electrically connects, signally connects, or both the interchangeable tip to a power source, a signal source, or both; and blade circuitry having: one or more control buttons, one or more switches, or both for controlling operation one or more functions of the interchangeable tip.

Abstract: A biopsy needle (80) having a longitudinal channel (84) formed within an inner conductor (86) of a coaxial antenna is disclosed. The coaxial antenna terminates in a rigid insertion tip (82) e.g. a ceramic cone that is insertable into biological tissue. Microwave energy (e.g. having a frequency of 1 to 100 GHz) delivered to the coaxial antenna is emitted at the insertion tip. The insertion tip may be arranged to match the impedance of the coaxial antenna to a predetermined tissue impedance. The emitted radiation can be used to measure properties of or treat (e.g. ablate) tissue at the insertion tip. Needle biopsy apparatus is also disclosed, in which a microwave energy is controllably delivered to a needle from a microwave generator. The apparatus may include an impedance tuner to dynamically match the impedance of the needle with tissue at the insertion tip.

Abstract: An electrosurgical instrument for removal of tissue from a patient and a method for doing the same. The electrosurgical instrument includes a pair of lever members each of which having an associated end effector associated. One of the end effectors includes a cutting element forming a loop on the end of the end effector. The cutting element is also configured to receive electrical energy from an electrical energy source. The other of the end effectors includes a pad that can be brought into a position generally opposing the cutting element during relative movement of the end effectors toward one another. When electrical energy is discharged from the cutting element and the end effectors moved toward one another, dissection and cauterization of tissue from a patient is facilitated.

Abstract: A system and method for powering a wireless electrosurgical device using a powered glove. The powered glove includes at least a conductive pad on a finger and a thumb. The glove is connected to a generator and supplies power to the wireless electrosurgical device when at least two conductive pads touch conductive buttons on the wireless device. The user selects the operating mode by selecting different combination of conductive buttons and/or switches on the wireless device. The generator senses a voltage drop across a circuit within the electrosurgical device to determine the operating mode. The generator then supplies the RF energy based on the selected operating mode via the glove to the wireless device.

Abstract: A device for forming a lesion includes a hub defining a passageway and a shaft attached to the hub and defining a lumen. The shaft has a proximal end and a distal end extending away from the hub. The shaft includes an electrically conductive material on at least a portion of an inner surface and on at least a portion on an outer surface. A conductive member has a longitudinal axis and is attached to a mounting structure mateable with mounting structure of the hub so that the conductive member extends through the passageway into the lumen so that at least near the hub the conductive member longitudinal axis is spaced from the lumen longitudinal axis to create electrical contact between the conductive member outer surface and the shaft inner surface.

Abstract: The invention pertains to techniques or processes for managing surgical smoke. In one embodiment a suction apparatus evacuates the surgical smoke. For example, the suction apparatus may be arranged adjacent to an electrocautery electrode, which may generate smoke during operation, for evacuating smoke from a surgical site.

Abstract: A device comprising: a handpiece having one or more attachment ports; a tubeset having one or more attachment features for connecting the tubeset to the one or more attachment ports in the handpiece; a removable tip having an attachment arm for attaching to the one or more attachment ports in the handpiece; wherein the device comprises one or more of the following: the handpiece includes an attachment port that attaches the handpiece to an active lead and a return lead and the device is adapted to use only the active lead or both leads so that the device can switch between bi-polar energy and mono-polar energy; the tubeset has one or more fluid conduits that are in fluid communication with the removable tip, wherein the removable tip is located at a distal end of the device; and the handpiece connects to one or more electrical input lines; the tubeset connects to one or more fluid lines, and the removable tip is free of direct connection to both the one or more electrical input lines and the one or more fluid

Abstract: An apparatus for deployment of a hemostatic clip comprises a handle assembly, a shaft connected to a distal portion thereof and a clip assembly releasably coupled to a distal portion of the shaft. The clip assembly includes clip arms and a capsule cooperating with the clip arms to provide a first user feedback indicating a decision configuration of the clip assembly. In addition, the apparatus includes a control wire including a ball connector, the control wire extending from the handle assembly and coupled to the clip assembly by the ball connector to maintain the clip assembly coupled to the shaft, wherein the ball connector is detachable from the clip assembly to provide a second user feedback indicating separation of the clip assembly from the shaft.

Abstract: A surgical instrument includes a handpiece, an elongate shaft extending distally from the handpiece, an end effector disposed at a distal end of the elongate shaft, and a firing beam. The end effector has a first jaw and a second jaw. The first jaw is pivotable toward and away from the second jaw to capture tissue. The end effector further comprises a preheating element and an electrode. The preheating element is configured to provide heat to the captured tissue, thereby increasing electrical conductivity of the tissue. The electrode is configured to seal the captured-preheated tissue by providing RF energy to the tissue. The firing beam is configured to sever the sealed tissue.

Abstract: An end effector for operating on tissue comprises a first jaw, a second jaw, a firing beam, and a support band. The first jaw is movable toward the second jaw to capture tissue. The first jaw has a first slot and the second jaw has a second slot. The firing beam and the support band are coupled together and are positioned to translate through the first and second slots of the jaws. The firing beam presents a sharp distal edge for severing tissue captured between the jaws. The support band presents a curved distal end. The sharp distal edge of the firing beam is partially covered and partially exposed by the curved distal end of the support band.

Abstract: A combination tissue coagulation and cutting apparatus, system and method for coagulating and cutting tissue. A clamp element includes first and second clamp members having respective first and second porous electrodes, such as sintered metal electrodes. A portion of tissue, such as a blood vessel, is held between the porous electrodes, and fluid from a fluid source can pass through the porous electrodes. The tissue portion can be coagulated when electrical current is applied to the first and second porous electrodes, and an adjustable cutting element that is associated with the clamp members is positioned to cut a segment or all of the coagulated tissue portion. In this manner, the same surgical instrument is used to coagulate and cut tissue.

Abstract: A surgical device and procedure for accessing tissue to perform microsurgery, including a capsulotomy of a lens capsule of an eye. The device includes a handpiece with a tip for insertion into an incision. A sliding element is disposed within the handpiece and a suction cup is mounted to the sliding element. The sliding element can be translated to move the suction cup into and out of the handpiece. A compression mechanism associated with the suction cup and the handpiece compresses the suction cup for deployment through the tip of the handpiece. The suction cup can expand inside the anterior chamber into a cutting position. A cutting element mounted to the suction cup is used to cut a portion and to remove the portion. The cutting element may be mounted to a cutting element support structure in a way that prevents heating of the device.

Abstract: A drive unit for a rotatable high-frequency electrode of a medical resector for cutting, ablating, or coagulating human or animal tissue includes an engine device for generating a rotation movement and a coupling device for transmitting the rotation movement generated by the engine device to an axis coupled with the rotatable high-frequency electrode when the drive unit is coupled with the medical resector. The drive unit is configured to provide on the coupling device a rotation frequency in a range from 10 rpm to 200 rpm.

Abstract: A system for targeting an operation site includes an identifier having an electromagnetic field generator configured to produce electromagnetic fields. The system includes an implement that includes a handle, a blade portion, and an electromagnetic field sensor coupled to the blade portion. The electromagnetic field sensor is configured to produce a signal responsive to electromagnetic fields produced by the electromagnetic field generator. The system includes a control unit configured to access information indicating a position of the electromagnetic field sensor relative to the operation site, receive a signal from the electromagnetic field sensor that is indicative of a position of a tool relative to the electromagnetic field sensor, and determine a position of the tool relative to an operation site based on the received signal and the position of the electromagnetic field sensor relative to the operation site.

Abstract: A clip-over disposable assembly includes a switch assembly and a disposable body. The disposable body includes a first disposable member, a second disposable member including first and second wall portions, and a third disposable member. The first wall portion defines a first aperture therethrough and a first cavity configured to receive therein a first portion of the switch assembly. The third disposable member includes a third wall portion, wherein a body of the second disposable member and the third wall portion define an opening configured to allow a shaft of a hemostat-style surgical instrument to pass therethrough. The second wall portion and the third wall portion cooperatively define a chamber in communication with the opening and configured to receive therein at least a portion of the shaft of the hemostat-style surgical instrument, wherein the at least a portion of the shaft is received in the chamber from an off-axis position.

Abstract: In surgery using monopolar HF, there is a constant risk of patients suffering burns at the neutral electrode. Said problem stems from the fact that numerous methods have been devised by which relatively high HF currents are applied for extended periods of time. The present invention solves said problem by providing a neutral electrode, device that is to be used for applying an HF current to a biological tissue. Said improved neutral electrode device comprises at least one latent heat accumulator for absorbing heat. Thus heat peaks can be at least temporarily accumulated until the accumulated thermal energy can be safely released.

Abstract: A tissue-resecting probe includes an elongated outer sleeve extending about an axis to a distal housing having a first window for receiving tissue. An edge of the first window has a dielectric surface. A rotatable inner sleeve has a second window, and at least a portion of an edge of the second window provides a first polarity electrode. Rotation of the inner sleeve within the outer sleeve moves the probe between window-open and window-closed configurations to resect tissue.

Abstract: Devices, systems, and methods for facilitating access to and visualization of the pancreaticobiliary system are disclosed. In particular, the present disclosure relates to devices used to expand and/or maintain the papilla opening to facilitate access therethrough, e.g., to visualize, examine, diagnose, and/or treat the bile duct and pancreatic ducts. The devices may include an elongate body, an expansion element having a compressed configuration and an expanded configuration, and an outer sheath.

Abstract: The present disclosure relates to a method and a device for treating heart failure by normalizing elevated blood pressure in the left and right atria of a heart of a mammal The present disclosure includes methods for creating and maintaining an opening in the atrial septum. Tools for making an opening and enlarging the opening are also disclosed. Use of the techniques and tools described herein prolongs the patency of an intra-atrial pressure relief opening.

Abstract: A method and apparatus for treating an intraosseous nerve. The method includes positioning a hollow shaft through the cortical shell of a vertebral body and into a cancellous bone region of the vertebral body. The hollow shaft includes an annular wall having a longitudinal bore therein, a proximal portion and a distal portion, and a first window extending transversely through the annular wall. An electrosurgical probe is advanced within the longitudinal bore from the proximal portion toward the distal portion. The electrosurgical probe includes a first treatment element at a distal end of the probe, wherein the first treatment element being in electrical connection with a power supply. The first treatment element is slidably disposed within the longitudinal bore so that the first treatment element is advanced radially outward from the window and shaft to affect treatment of the intraosseous nerve within the cancellous bone region.

Abstract: Systems and methods are provided for treating chronic pain occurring secondarily to subacromial impingement syndrome in a human body. A system is provided to deliver percutaneous electrical stimulation through at least one electrode to neurological motor points of the posterior and middle deltoid muscles to mediate such pain. One-time, continued and/or periodic dosing of treatment methods according to the present invention may result in a change to central nervous system maladaptive neuroplasticity.

Abstract: In various embodiments, a surgical instrument is provided that may comprise an end effector for performing a surgical procedure on tissue, for example. The end effector may comprise a pair of jaws, a closure beam, and a cutting member. The closure beam and the cutting member may be releasably coupled together by an interlocking member such that movement of the cutting member may cause the closure beam to also move relative to the jaws and cause the jaws to close and grip tissue, for example. The interlocking member may then unlock, allowing the cutting member to move through the gripped tissue and relative to the closure beam. Additionally, the cutting member and closure beam may be operated by a single trigger, which may be configured to provide haptic feedback to a user at various stages. Further, the jaws may be electrically energized to deliver energy and/or seal the gripped tissue.

Abstract: A magnetically-guided catheter 100 includes a tip positioning magnet in the distal electrode assembly configured to interact with externally applied magnetic fields for magnetically-guided movement. A magnetically-guided mapping catheter 100 includes an electrically-conductive capsule in the form of a casing 146 that includes a distal ablation surface and isolates the positioning magnet from bio-fluids to prevent corrosion. An open irrigation ablation catheter includes an isolated manifold that isolates the positioning magnet from contact with irrigation fluid to prevent corrosion.

Abstract: A surgical clamp including a pair of jaws, which may be used to ablate or create lesions in tissue. In an exemplary embodiment, the jaws are movable between an articulated position in which the jaws are separated and not parallel to one another, an opened position in which the jaws are separated and substantially parallel to one another, and a closed position in which the jaws are adjacent and substantially parallel to one another.

Abstract: A resector balloon includes an outer wall having a resecting surface that resects biological material. The balloon also includes a woven sleeve including at least one woven thread disposed on at least a portion of the outer wall. The woven sleeve forms at least a portion of the resecting surface. In certain embodiments, the woven sleeve includes weft knit threads including crossover points where the threads overlap. In some embodiments, the woven sleeve includes electrically conductive threads.

Abstract: Methods of treating the sacroiliac region of a patient's body by delivering energy are described. In some embodiments, the method comprises the steps of: inserting at least one probe into the sacroiliac region, the probe comprising at least one energy delivery device: positioning the at least one energy delivery device adjacent material to be treated; and delivering energy through the at least one energy delivery device to create a longitudinal strip lesion; wherein the at least one energy delivery device remains in a substantially static position during creation of the strip lesion. In some embodiments, energy may be delivered to treat at least two branches of the sacral nerves or to create an intra-articular lesion.

Abstract: A contact sensing assembly including a catheter including an electrode having a base portion mounted adjacent a head portion of the catheter body. A sensor is disposed adjacent the base portion for measuring compression or tensile forces applied to an electrode tip portion, and includes a predetermined sensitivity. The base and head portions include predetermined rigidity so that forces applied to the electrode tip portion are determinable as a function of the sensitivity and a sensor output. A contact sensing assembly also includes an electrode pipe operatively connected to the catheter body for movement and bending with the catheter body, and an electrode wire disposed in the electrode pipe and including insulation. A change in capacitance resulting from movement of the electrode wire toward the electrode pipe or contact of the electrode wire with the electrode pipe during bending of the catheter correlates to a force applied to the catheter.

Abstract: A combined electrical tissue sealing and mechanical tissue cutting instrument. The instrument has two opposing jaw members. A removable cartridge is positioned in one of the jaw members. The cartridge includes a tissue sealing electrode and a tissue cutter. As either the tissue sealing electrode or the cutter deteriorates with use, the cartridge is replaced with a new cartridge. Cartridges are configured with various electrode geometries to accommodate various associated electro-surgical units. One or more pressure sensors in the cartridge or in the instrument jaw that supports the cartridge provide an indication that a required clamping pressure exists between the jaw members to carry out the tissue sealing. A cut and seal controller allows various actions to be carried out when particular clamping pressures are sensed, or when an indication that tissue sealing is complete is sensed.

Abstract: A high-frequency treatment apparatus includes an insertion portion, a covering portion provided in a distal end portion of the insertion portion, an electrode portion provided in the covering portion, through which high-frequency current is to flow, including a side treatment portion arranged along an outer surface of the covering portion and a distal end treatment portion formed of a distal end portion of the electrode portion, and configured to be moved between a forward position where the distal end treatment portion is protruded from the covering portion with respect to a forward and backward movement direction and a backward position where the distal end treatment portion is arranged within the covering portion with respect to the forward and backward movement direction, and an operation member inserted through the insertion portion and connected to the electrode portion wherein the electrode portion is configured to be moved by operating the operation member.

Abstract: A treatment system comprises an outer sheath and an end effector. The end effector has a plurality of cutting features, at least a portion of which are configured to debride a tissue surface when the end effector is actuated. The cutting features may also be configured to harvest tissue. A medical fluid reservoir is in fluid communication with the end effector, such that the end effector may deliver a medical fluid to a target site such as a fistula. The medical fluid may include harvested tissue cells and a scaffold material. A vacuum cannula may be positioned coaxially within the interior cavity of the end effector, and an RF probe may be positioned co-axially within the interior cavity of the vacuum cannula. The vacuum cannula and RF probe may be used together to seal a fistula in which medical fluid has been dispensed.

Abstract: An endoscope treatment tool includes a sheath having electric insulation; and an electrode unit provided at a distal end portion of the sheath. The electrode unit includes a rod-shaped electrode that is provided to extend in an axis direction of the sheath and is capable of being arranged in a state where the electrode protrudes from the distal end portion of the sheath and is exposed to the outside; and a chip that is fixed in a state where a distal end portion of the electrode is inserted into a concave portion provided in a proximal end surface so as to extend in the axis direction, has a greater external diameter than the external diameter of the electrode, and is formed from a single electric insulation material. The concave portion is formed with a smaller-diameter portion that allows the distal end portion of the electrode to be inserted thereinto.

Abstract: A system for monitoring ablation size is provided and includes a power source including a microprocessor for executing at least one control algorithm. A microwave antenna is configured to deliver microwave energy from the power source to tissue to form an ablation zone. A radiation detection device is operably disposed on the microwave antenna. The radiation detection device is configured to generate a voltage corresponding to a radius of the ablation zone, wherein the radiation detection device is in operative communication with at least one module associated with the power source. The at least one module triggers a signal when a predetermined threshold voltage is measured corresponding to the radius of the ablation zone.

Abstract: A suction apparatus evacuates the surgical smoke. For example, the suction apparatus may be arranged adjacent to an electrocautery electrode, which may generate smoke during operation, for evacuating smoke from a surgical site. The suction apparatus may have a ring manifold having an inner perimeter for receiving the surgical instrument. A plurality of suction intake ports may be arranged about the outer perimeter of the ring manifold for evacuating smoke that may be generated by the surgical instrument.

Abstract: The invention relates to electrodes used in ablation catheter devices, where the electrodes contain two or more thermal sensors at different positions within the electrode that are capable of detecting temperature differences along the external surface of the electrode. In preferred embodiments, the thermal sensors are separated by one or more thermal insulating members and the thermal sensors are positioned near the external surface of the electrode at about the same distance from the end of the electrode, so that temperature measurements can indicate the position of the electrode with respect to the tissue desired to be ablated.

Abstract: A high-frequency knife conduit line and opening hole opening communicate allowing fluid to flow between a rod-shaped electrode outer peripheral surface and the opening hole inner peripheral surface. The guide hole is smaller than the opening and is further toward a radial inner side than the opening outer edge and further toward a radial outer side than the rod-shaped electrode. The fluid is released from the opening to the outside of the sheath over the whole circumference of the rod-shaped electrode on the radial outer side while an electrode portion protrudes toward the sheath distal end portion separating a larger-diameter portion from a supporting member. The fluid is injected to the larger-diameter portion front through the guide hole as the opening hole and the guide hole communicate while the electrode portion is pulled back toward the sheath proximal end portion so that the larger-diameter portion abuts against the supporting member.

Abstract: An apparatus comprises a body, a shaft assembly, and an end effector. The shaft assembly extends distally from the body. The end effector is in communication with the shaft assembly. The end effector comprises a first jaw and a second jaw. The second jaw comprises a proximal portion and a distal portion. The second jaw is moveable relative to the first jaw between a first position, a second position, and a third position. The second jaw in the first position is open relative to the first jaw. The second jaw in the second position is positioned such that the distal portion is closer to the first jaw than the proximal portion. The second jaw in the third position is parallel the first jaw.

Abstract: A treatment portion of a treatment device includes a pair of jaws, an energy emitter, a base having has electric insulation, an outer edge, first to third channels and a support portion. The first channel is formed by the energy emitter, the base, and the outer edge, fluid emanating from the living tissue of the treatment target flows into the first channel. The second channels are provided between the base and the outer edge. The third channel is provided between the outer edge and the energy emitter to allow the fluid emanating from the living tissue to flow toward the first channel. The support portion couples the base to the outer edge so that the fluid emanating from the living tissue flows into the first channel, and supports the living tissue to prevent it from coming into the first channel when it is held between the pair of jaws.

Abstract: In the case of an instrument (10) for coagulation and fusion as well as for severing vessels, provision is made for two shanks (19, 20), between which a vessel is to be gripped and fused. A blade (21) for severing the coagulated and fused vessel is provided with an isolator (40), which isolates the blade (21) against at least one of the electrodes or shanks (19, 20), respectively. On the other hand, the blade (21) is preferably in mechanical contact with at least one of the electrodes or shanks (19, 20), respectively, so that a safe separation of the fused biological tissue or vessel, respectively, is attained. This concept can be used to increase the safety of surgery and to miniaturize the tool (18) towards smaller sizes.

Abstract: An electrosurgical forceps is provided with a shaft that extends from a housing of the electrosurgical forceps. An end effector assembly operably coupled to a distal end of the shaft includes a pair of first and second jaw members having proximal and distal ends. One or both of the first and second jaw members is movable from an open configuration for positioning tissue therebetween, to a clamping configuration for grasping tissue therebetween. A knife blade assembly includes a knife blade that is translatable within the first and second jaw members when the first and second jaw members are in the clamping configuration. The knife blade assembly includes a knife blade stop configured to contact at least a portion of the proximal end of the second jaw member when the first and second jaw members are in the open configuration to limit translation of the knife blade assembly.

Abstract: A surgical instrument includes a first member having an inner surface defining a first passageway. A second member is disposable within the first passageway and movable relative to the first member. The second member defines a longitudinal axis and extends between a first end and a second end configured to engage tissue. The second end includes a first surface configured for a non-penetrating engagement with the tissue and a second surface including at least two spaced apart cutting members extending axially from the first surface. The cutting members are rotatable to excise a portion of the tissue. Systems and methods are disclosed.

Abstract: An electrosurgical device comprising: forceps including: (i) a first working arm having a contact surface and (ii) a second working arm having a contact surface; wherein the forceps has a first electrical configuration where the contact surface of the first working arm and the contact surface of the second working arm are substantially opposite each other so that the contact surfaces of the forceps can be used to grip an item between the working arms and so that the forceps is configured to deliver a first therapy current through the first working arm, the second working arm, or both; and wherein the forceps has second electrical configuration where the contact surface of the first working arm and the contact surface of the second working arm are askew relative to each other and an electrode edge is formed on at least one side of the forceps so that a second therapy current extends from the electrode edge.

Abstract: A novel device and method for surgical inducement of cervical vertebra fusion as a treatment for cervical spinal disease using a guide wire, slide knife, and a minimally invasive portal access device and an inter-vertebra linking member.

Abstract: A medical resector for oblating, cutting, or coagulating human or animal tissue includes a rotatable high-frequency electrode on the distal end of a shaft of the medical resector and an axle that runs from the proximal end to the distal end of the shaft and is mechanically coupled with the high-frequency electrode on the distal end. The axle is positioned on the distal end of the shaft in the center or as close as possible to the center of the cross-section of the shaft and on the proximal end of the shaft on the border or as close as possible to the border of the cross-section of the shaft.

Abstract: A medical device for treating and analyzing tissue is disclosed. The device includes a plasma applicator having a housing. The housing includes a substantially tubular shape and defining a lumen therethrough. The lumen is in fluid communication with an ionizable media source configured to supply ionizable media thereto. The applicator also includes one or more electrodes coupled to the housing. The electrodes are adapted to couple to a power source configured to that energizes electrodes to ignite the ionizable media to form a plasma plume for treating tissue. The device also includes an effluent-collection attachment coupled to the plasma applicator, the effluent-collection attachment configured to collect at least a portion of a plasma effluent.

Abstract: An apparatus comprises a catheter, a conductive element and a balloon. The catheter has a lumen. The conductive element is disposed along the catheter. The balloon has an interior in fluid communication with the lumen of the catheter. The balloon is formed of a conductive material conductively coupled to the conductive element. The balloon has a collapsed configuration and an expanded configuration.

Abstract: Various embodiments of a capsulotomy repair device include a resistive-heating element comprising an electrically resistive, superelastic wire forming a loop between first and second ends of the superelastic wire. The first and second ends of the loop may at least partially extend at an angle from a planar face defined by the loop, to an insulating portion, to form a transitional neck between the loop and the insulating portion. The capsulotomy repair device may be positioned in the eye relative to a capsularhexis perimeter to overlap tears in the capsularhexis perimeter to remove the tears by forming an adjusted capsularhexis perimeter by burning around the tear.

Abstract: An electrosurgical device coated with powder coatings including a silicone resin and siloxane additive without fluoropolymers. In the powder coatings, the silicone resin is methyl phenyl silicone or phenyl silicone or methyl polysiloxane or phenyl alkyl polysiloxane resin and the additive is either methyl alkyl polysiloxane or dimethyl polysiloxane. This coating is applied to the surfaces of an electrosurgical device minimize the build-up of charred tissue on the surfaces of the electrosurgical device.

Abstract: An electrosurgical device coated with powder coatings including a silicone resin and siloxane additive without fluoropolymers. In the powder coatings, the silicone resin is methyl phenyl silicone or phenyl silicone or methyl polysiloxane or phenyl alkyl polysiloxane resin and the additive is either methyl alkyl polysiloxane or dimethyl polysiloxane. This coating is applied to the surfaces of an electrosurgical device minimize the build-up of charred tissue on the surfaces of the electrosurgical device.