Abstract: A rechargeable cleaner includes a body, a rechargeable battery, and a charger. The body is configured to generate suction power capable of sucking dust together with air using a motor. The rechargeable battery is configured to supply electric power to the motor. The charger is configured to charge the battery at a charging rate of 3 C or higher and lower than 10 C.

Abstract: The disclosure extends to methods, devices, and systems for removing speckle from a coherent light source, such as laser light. The methods, devices, and systems help eliminate or reduce speckle introduced from a coherent light source, such as laser light, by utilizing the teachings and principles of the disclosure.

Abstract: A handheld end of an endoscope includes a housing, an insertion end positioning assembly and a self-locking assembly. The self-locking assembly is hinged to the housing. The housing includes an insertion port. The insertion end positioning assembly includes a positioning member, a first positioning nut and a threaded steel tube. The positioning member is inserted into the insertion port. The threaded steel tube is in threaded fit with the first positioning nut. The first positioning nut is fixed in the positioning member. The insertion end positioning assembly further includes a through hole and a fixing member. The fixing member is fit with the through hole to abut against the threaded steel tube. The threaded steel tube is fit with the positioning member to fix an axial position of the positioning member. A second nut is fit with a fixing screw to fix a rotational position of the positioning member.

Abstract: An endoscope device includes a hollow tube, a thermal-conductive member, an image-capturing module, and a heat-dissipation tube. The hollow tube includes an insertion end. The thermal-conductive member is in the hollow tube and adjacent to the insertion end. The thermal-conductive member includes a first end, a second end, and a receiving groove. The first end is near to the insertion end as compared with the second end, and the receiving groove is between the first end and the second end. The image-capturing module includes a camera module and a circuit board in the receiving groove. The camera module is at the insertion end and electrically connected to the circuit board. The first end contacts the camera module. The heat-dissipation tube is in the hollow tube. One end of the heat-dissipation tube contacts the thermal conductive member, and the other end of the heat-dissipation tube extends away from the insertion end.

Abstract: An endoscope includes: an objective optical system including a lens, allowing light from an imaging subject to be incident on a distal end surface, and focusing the light onto an image-capturing surface of an image-capturing element; an elongated light guide provided adjacent to a side of the system and guiding illumination light to be emitted from a distal end; and an optically transparent distal end cover disposed at a position where the distal end of the guide is covered, wherein the distal end surface is located farther forward than the distal end of the guide, a notched portion is provided at a distal-end outer edge of a side surface of the system, the side surface being adjacent to the guide, so that the system is narrower toward a front side from the distal end of the guide, and the cover is provided so as to bulge toward the notched portion.

Abstract: An endoscope apparatus includes: an endoscope distal end portion including an optical system configured to form an optical image, an image sensor configured to generate an image signal in accordance with a predetermined frame rate when the optical image is input, and an actuator configured to move the optical system along an optical axis; and a controller electrically connected to the endoscope distal end portion and including an imaging circuit configured to acquire the image signal from the image sensor, a drive circuit configured to feed a drive voltage to the actuator, and a processor configured to control the imaging circuit and the drive circuit, detect a vertical blanking period of the image signal acquired by the imaging circuit based on the image signal, and control the drive circuit to gradually increase a voltage supplied to the actuator within the vertical blanking period.

Abstract: An endoscope treatment tool includes: a cylindrical distal-end member to be attached to a distal end of an endoscope; a grasping tool that is provided at an outer side surface of the endoscope along a longitudinal axis of the endoscope, that grasps biological tissue, and that is movable in a first direction perpendicular to the longitudinal axis in a state in which the biological tissue is grasped; an electrode that is disposed so as to protrude forward with respect to a distal end of the distal-end member; and an electrode driving portion that is configured to move the electrode in the first direction.

Abstract: An endoscope in which a reusable part is inserted into a sheath of a single-use portion that includes a needle with an imaging module at its tip and a part of the reusable portion that is not covered by the sheath is covered with a flexible cap that initially was sterile and covered the open end of the sheath, whereby the entire reusable portion is covered and sealed from the environment by the cap and the sheath during a medical procedure.

Abstract: The present disclosure relates to the field of medical devices. Specifically, the present disclosure relates to devices, systems and methods for extending a working channel of an endoscope, such as for delivery of a stent.

Abstract: A method comprises measuring, with a sensor, a shape of a section of an elongated flexible instrument and comparing the measured shape of the section of the elongated flexible instrument to an expected shape. The method also comprises determining whether the measured shape of the section of the elongated flexible instrument differs from the expected shape by a predefined threshold.

Abstract: A channel device is disclosed for transporting gas and/or liquid between a control unit and a scope accessory, the channel device comprising a wash line, the wash line comprising: a wash line gas channel; a wash container; a piston; and a wash line wash channel, the wash line gas channel being configured to receive a gas from a wash line gas output of the control unit, the piston being configured to be actuated due to an increase in pressure in the wash line gas channel caused by the received gas to cause a liquid to be expelled from the wash container, the wash line wash channel being configured to transport the expelled liquid to the scope accessory.

Abstract: A channel device is disclosed for transporting gas and/or liquid between a control unit and a scope accessory, the channel device comprising a wash line, the wash line comprising: a wash line gas channel; a wash container; a piston; and a wash line wash channel, the wash line gas channel being configured to receive a gas from a wash line gas output of the control unit, the piston being configured to be actuated due to an increase in pressure in the wash line gas channel caused by the received gas to cause a liquid to be expelled from the wash container, the wash line wash channel being configured to transport the expelled liquid to the scope accessory.

Abstract: The technology described herein can be embodied in a method that includes receiving data representing information captured using a first sensor and a second sensor of a multi-sensor camera. The sensors are configured to capture a surgical scene illuminated by a light source configured to emit wavelengths in the visible spectrum corresponding to sensing capabilities of the first and second sensors, respectively. The method also includes receiving data representing information captured using a third sensor of the multi-sensor camera, the third sensor configured to capture the surgical scene as illuminated by a near-infrared light source, and generating a first visual representation of the surgical scene based on the data representing the information captured using the first and second sensors. The first visual representation is combined with the information captured using the third sensor to generate a second visual representation, and the second visual representation is presented on a display device.

Abstract: A medical control apparatus to which a rigid endoscope having an insertion portion to be inserted into a subject is detachably connected is configured to perform image processing on a captured image obtained by capturing a subject image introduced by the rigid endoscope and generate a medical photographic image to be displayed on a display device that displays images. The medical control apparatus includes: a detection unit configured to detect a mask width that is a distance between boundary points dividing the subject image included in the captured image and a mask area that is an area other than the subject image; and a control unit configured to calculate a first parameter used for the image processing in accordance with the mask width.

Abstract: An endoscope has an improved chip-on-tip configuration that includes both a first configuration of source illumination fibers and a second plurality of source illumination fibers, along with a camera chip. The combination of the camera chip and the source illumination fibers on the tip of the endoscope results in endoscopes with reduced size and weight.

Abstract: Systems, devices, and methods for identifying a target during an endoscopic procedure are disclosed. An endoscopic target identification system includes an endoscope having an endoscopic illumination source, an optical fiber insertable through a working channel of the endoscope and coupled to a non-endoscopic illumination source different from the endoscopic illumination source, and a controller. The controller can send a control signal to the non-endoscopic illumination source to emit a diagnostic beam through the optical fiber when the at least one endoscopic illumination source changes from a first mode to a second mode. The second mode has a lower amount of illumination than the first mode. The controller can determine a composition of a target based on the diagnostic beam incident on the target and light from the diagnostic beam being reflected from the target.

Abstract: A device for visible puncture includes a balloon, a canula, a needle tube, an image acquisition device, and a fluid injection tube. The balloon includes a first end including a first hole, and a second end including a second hole. The canula includes a first axial through hole. The needle tube includes a second axial through hole and is disposed in the first axial through hole. The image acquisition device is disposed in the second axial through hole. The balloon is axially disposed on the canula. The first end of the balloon is disposed on the outer wall of the front end of the needle tube, and the second end of the balloon is disposed on the outer wall of the front end of the canula. The second axial through hole includes a fluid channel disposed between the outer wall of the needle tube and the canula.

Abstract: A nasal irrigation diagnostic assembly comprising an irrigation device including a fluid collection portion structured to retain a biological sample, in the form of waste solution from the nasal cavity resulting from irrigation. A detection member disposed on said irrigation device is exposed to the biological sample and is structured to determine the existence of at least one analyte within the biological sample of the waste solution. The detection member comprises a plurality of detection zones individually structured to analyze the biological sample upon engagement therewith, wherein said plurality of zones include at least a reaction zone and a detection zone, which respectively include reagents cooperatively and collectively formulated to detect the existence of the at least one analyte within biological sample of the waste solution. A control zone may also be included to indicate the intended operability of at least the detection member.

Abstract: A medical mechatronic male interface device couples a surgical assistance system to a mount. The male interface device includes a base including an end face and a functional body extending from the end face, a first mechanical coupling for positive and/or non-positive coupling to a medical mechatronic female interface device, and at least one first electronic interface configured to connect to a second electronic interface of the female interface device. The functional body includes a centering device that centers the surgical assistance system free of play relative to the base. The centering device includes a first functional surface, a second functional surface, and a third functional surface that together at least partially define a three-sided pyramid. The first mechanical coupling includes a first undercut and a second undercut on the functional body that each define a segment engageable from behind.

Abstract: A device for joining two layers of tissue, comprises a substantially flat and flexible scaffold having an upper surface, a lower surface and sidewalls; a plurality of first passages penetrating said scaffold from said upper surface to said lower surface; a plurality of second passages penetrating said scaffold from said upper surface to said lower surface; a substantially flat and flexible top cover releasably attached to said upper surface and covering all of said upper surface; said top cover having a plurality of top cover passages aligned with said first plurality of passages.

Abstract: The present disclosure relates generally to the field of medical devices. In particular, the present disclosure relates to a tissue traction device, e.g., for an endoscopic procedure such as endoscopic tissue dissection. For example, a tissue traction device may include a traction band having a first end, a second end, a length therebetween and extending along a longitudinal axis. A first attachment member may extend from the first end of the traction band. A second attachment member may be associated with the body between the first end and the second end of the traction band. A third attachment member may extend from the second end of the traction band.

Abstract: A retraction system and method are provided for retracting tissues surrounding a surgical site. In one aspect, a method including engaging slide connections between a guide dilator and a plurality of tissue engaging members and sequentially enlarging an incision using the guide dilator and the plurality of tissue engaging members. In another aspect, a method of inserting a plurality of tissue engaging members into an incision including fixing tip portions of the plurality of tissue engaging members in an insertion configuration, advancing the tip portions into an incision, and restricting movement of the tip portions away from the insertion configuration. A guide dilator system comprising an elongate body, a plurality of tissue engaging members, and slide connections between the elongate body and the tissue engaging members is also provided.

Abstract: Various devices, systems, and methods are provided for securing soft tissue to bone. In one exemplary embodiment, a two-piece inserter tool is provided that includes a tip portion that is configured to be removably coupled to a handle portion. A distal portion of the tip portion can be configured to be coupled to a suture anchor, and the tip portion and the anchor can be passed through a continuous suture loop prior to mating the tip portion to the handle portion.

Abstract: A mechanical suture fastener includes a crimpable sleeve defining a channel therein. The crimpable sleeve also has a sleeve length, a channel diameter, and a sleeve length to channel diameter ratio of at least 4.0. The mechanical suture fastener also includes a flange joined to the crimpable sleeve on a distal end of the sleeve. The flange further includes a distal opening which is in communication with a proximal opening defined by the crimpable sleeve. The mechanical suture fastener also includes an inner flange radius of at least 0.007 inches.

Abstract: A bi-directional medical suturing device includes a first needle; a second needle being disposed distal to the first needle; a first thread control member including a first holding portion being movable between a position where the first holding portion prevents a movement of the first needle and a position where the first holding portion does not prevent the movement of the first needle; and a second thread control member including a second holding portion being located the first holding portion, the second holding portion being movable between a position where the second holding portion prevents a movement of the second needle and a position where the second holding portion does not prevent the movement of the second needle.

Abstract: Devices, systems and/or methods for repairing soft tissue adjacent a repair site. In one embodiment, a repair device is delivered with a delivery device system configured to move a cartridge with the repair device disposed therein toward an anvil with soft tissue positioned thereon. The delivery device linearly moves the cartridge toward the anvil with a worm drive positioned within a housing by rotating a thumb wheel disposed around the worm drive. Such linear movement is provided with a finger element extending from the worm drive that is configured to cooperate with an internal surface of the thumb wheel. With this arrangement, upon rotating the thumb wheel, the worm drive rotates with the finger element engaged with the internal surface of the thumb wheel to linearly move the cartridge toward the anvil.

Abstract: The present disclosure provides a closure driving mechanism and a medical stapler including the same. The closure driving mechanism includes a driving part and a cylinder body, the driving part is connected with a closure pulling sheet of the stapler, and a cavity provided with a one-way valve is formed inside the cylinder body. When the driving part moves toward a distal side of the stapler, a volume of the cavity is decreased, the one-way valve is closed, and the driving part drives the closure pulling sheet to move distally, so as to open a head assembly of the stapler. Since the driving part is subjected to a resistance of compressed air in the cavity, a movement speed of the driving part is decreased, and the head assembly is opened slowly to prevent a force of opening the head assembly being too large to damage surrounding tissues.

Abstract: A surgical system comprising a stapling instrument and a staple cartridge including a plurality of independent circuits powered by the surgical instrument is disclosed.

Abstract: A surgical stapling assembly is disclosed. The assembly can include a cartridge body having cavities defined therein forming a pattern of openings in the deck of the cartridge body. The pattern can include longitudinally-repeating clusters of cavity ends. The assembly can also include fasteners removably positioned in the cavities. The pattern of openings can comprise openings on a first side of the cartridge body comprising inner openings each defining an inner proximal-to-distal axis oriented parallel to the longitudinal axis, outer openings each defining an outer proximal-to-distal axis obliquely-oriented relative to the longitudinal axis at an outer angle, and intermediate openings each defining an intermediate proximal-to-distal axis obliquely-oriented relative to the longitudinal axis at an intermediate angle, wherein the intermediate angle is different than the outer angle.

Abstract: A surgical stapling device (10) includes a replaceable cartridge assembly (44) having knife assembly (80) and an anvil assembly (42) including a cutting plate (52). The cutting plate (52) is configured be durable to maintain performance of the stapling device (10) over multiple firings.

Abstract: To provide a surgical clip capable of being held by, in particular, a robot arm or other device, thus promoting automation of a procedure. A surgical clip to pull an organ or other body tissue so as to provide an area necessary for an operation includes: a pair of upper and lower holders to hold the organ or other body tissue therebetween; a grip to open and close the holders; an urger to constantly urge the holders in a holding direction; and an engagement portion provided on the grip. The engagement portion comes into engagement with a hole defined in a functional part provided on a medical device that includes any one of a robot, forceps, and an applier. The functional part is configured to open and close so as to perform a holding, incising, or other operation.

Abstract: A surgical stapling system comprising an actuator system operable to generate independent motions and a stapling end effector responsive to the independent motions generated by the actuator system is disclosed. The stapling end effector comprises a staple cartridge jaw comprising a plurality of staples removably stored therein, an anvil jaw, and a firing member. The firing member comprises an anvil-engaging portion and a cartridge jaw-engaging portion configured to engage the staple cartridge jaw.

Abstract: Implantable medical devices for connecting tissue layers, such as for connecting a gallbladder and a portion of a gastrointestinal tract to create an anastomosis, include a tubular structure having a plurality of apposition portions, a central region, and a covering material. The methods of using the devices include endoscopic deployment, and the devices may include self-expanding frameworks that facilitate a secure connection between the tissue structures.

Abstract: The present disclosure relates to a device for assisting in communicably coupling a first organ body with a second organ body by employing a plurality of arc-shaped tissue connector devices comprising a tissue connector body with a proximal and distal end, and a method for manufacturing such a device. The device comprises a curved frame having a principle axis and configured to embrace, at least partially, the first organ body, the curved frame configured to receive a plurality of tissue connector devices which extend from a proximal end thereof coupled to the curved frame and terminate in a free distal end. The disclosure further relates to a tissue connector device, a holder for tissue connector devices and a tissue-collar manipulating device, and a method of coupling a first and a second organ body using such device.

Abstract: A pulmonary artery flow restrictor system includes a funnel shaped membrane with a proximal base and a restrictive distal opening which is stretchable to larger sizes. A self-expanding frame is attached to the proximal base of the membrane for securing the membrane within the pulmonary artery.

Abstract: Some systems and methods for treating heart tissue may include instruments for intermittently occluding the coronary sinus using a coronary sinus occlusion catheter device. In some embodiments, the coronary sinus occlusion catheter can be used before or during a coronary intervention procedure in which a blockage in a heart is repaired or removed.

Abstract: An indwelling clip includes a clip main body having a pair of arm plate portions that can be opened in a substantially V shape with an elastic force and claw portions formed on respective tip portions of the arm plate portions. The indwelling clip also includes a fastening ring attached to the arm plate portions so as to be movable along a longitudinal direction of the pair of arm plate portions and be able to close the pair of arm plate portions by moving in a direction of the claw portions. An outer surface of the claw portion is provided with a fluorescent body containing a fluorescent pigment emitting red or near infrared light by being irradiated with excitation light.

Abstract: An all-in-one osteotomy fixation device, along with various related components, systems, and methods. The various embodiments include a device body, a bone attachment structure, a removable slot body, and a movable cutting guide moveably attached to the body via a guide coupling structure. The various methods include using any single device embodiment herein to perform all of the steps of the osteotomy procedure.

Abstract: A surgical assembly, a stabilisation plate and methods. The surgical assembly comprises includes a jig having a body with a tissue-engaging surface shaped to be received by tissue to be re-orientated by a correction factor. The body defines a plurality of alignment apertures orientated to be parallel with respect to each other on application of said correction factor.

Abstract: Methods and apparatus for performing a discectomy are disclosed herein. In some embodiments, a surgical tool for use in a therapeutic treatment of a patient includes a handle; an upper arm coupled to the handle; a lower arm coupled to the handle; a pivot arm coupled to one of the upper arm or the lower arm via a first pivot pin; and an end effector pivotably coupled to the pivot arm via a second pivot pin, wherein actuation of the handle causes movement of the pivot arm and articulation of the end effector.

Abstract: There is provided herein and improved anterior cruciate ligament reconstruction technique which comprises drilling a guide wire straight through a tibial passage and then at an angle from an ACL insertion point straight through a femoral passage. A reamer is then attached to a proximal end of the guidewire. The reamer has a distal cutting head, a distal flexible shaft, a proximal cutting head and a proximal flexible shaft. The proximal cutting head has a greater diameter than that of the distal cutting head. The reamer is drilled to follow the guidewire until the distal cutting head passes through the femoral cortex. The reamer is then retrieved at a proximal end thereof, thereby having created a larger diameter medial passage portion and a smaller diameter lateral passage portion within the femoral passage in a single pass, thereafter being ready for insertion of a graft, including by endobutton fixation.

Abstract: A guide for a bone cut comprises a guide base having an inner wall defining an opening. The inner wall has a plurality of detents distributed around the opening. The guide base has a proximal surface adapted to contact a skin of a person. An inner collar has one or more spring loaded devices extending outward from the inner collar in opposite directions. The inner collar is mountable with the spring loaded devices fitting within one or more of the plurality of detents. The inner collar has an inner wall defining a bore for receiving a cutting tool. The inner collar is configured to pivot the cutting tool about an axis, for cutting a bone. The axis lies along or parallel to a line along which the spring loaded devices lie.

Abstract: A system for preparing an ankle bone to receive an ankle prosthesis is provided. The system includes a patient specific cutting guide that has an anterior surface, a posterior surface, and at least one cutting feature extending through the guide from the anterior surface. The posterior surface comprising a first protrusion or other member that extends from a first end fixed to the posterior surface to a second end disposed away from the first end of the first protrusion. The posterior surface has a second protrusion or other member that extends from a first end fixed to the posterior surface to a second end disposed away from the first end of the second protrusion. The first and second protrusions are spaced apart and have a length such that when the patient specific cutting guide is coupled with first and second bone references, which can include bushings implantable in bones, a clearance gap is provided between the posterior surface and the ankle bone.

Abstract: A device includes: a sheath; an operating wire disposed inside the sheath; a grasping part that is provided at a distal end of the operating wire and that has one or more wires; and a bipolar electrode disposed at a distal end of the sheath. The sheath has, at intervals in the circumferential direction, escape grooves that extend from the distal end toward a proximal end of the sheath, that penetrate from an inner circumferential surface to an outer circumferential surface thereof, and that have such dimensions as to allow the wires to pass therethrough. The bipolar electrode is disposed at a position shifted radially outward from the central axis and at a position between two of the escape grooves in the circumferential direction. The distal end of the bipolar electrode is positioned closer to distal ends of the escape grooves than to proximal ends of the escape grooves.

Abstract: A clot removal device for removing clot from a body vessel comprising an expandable structure and an elongate member. The elongate member can have a proximal end and a distal end, the elongate member being connected to the expandable structure at its distal end. The expandable structure can have a constrained delivery configuration, an expanded clot engaging deployed configuration, and an at least partially constrained clot pinching configuration. At least a portion of the expandable structure can be configured to engage clot in the expanded deployed configuration and to pinch clot on movement from the deployed configuration to the clot pinching configuration.

Abstract: An intraluminal device may be provided including an elongated structure formed of a plurality of wires. The intraluminal device may include at least one expandable mesh segment configured to engage an obstruction in a body lumen, wherein the plurality of wires may be arranged into sets of looped wires that overlap to form the expandable mesh segment. The intraluminal device may also include at least one clot anchoring segment that may be configured to trap the obstruction to prevent downstream movement of the obstruction relative to the intraluminal device.

Abstract: Fluid management in surgical procedures. At least some of the illustrative embodiments are methods including: supplying fluid to a surgical site inside a patients body, drawing fluid from the surgical site through a first instrument by a first pump at a first flow rate, the first flow rate during the drawing responsive to expected or actual visibility within the surgical site; and then performing a surgical resection within the surgical site using the first instrument, the performing the surgical resection changes the first flow rate; and adjusting, by a fluid management system after the surgical resection, the first flow rate responsive to the expected or actual visibility within the surgical site.

Abstract: A tissue-resecting end effector includes an outer shaft having a hub housing, an inner shaft including a sun gear, and a drive assembly disposed within the hub housing. The drive assembly includes a first and second drivers disposed about the inner shaft distally and proximally of the sun gear, respectively. The drive assembly further includes a plurality of planetary gears radially disposed about and in meshed engagement with the sun gear between the drivers, and a locking clip proximal of the planetary gears and the sun gear, rotationally keyed to the second driver, and engaged with the first driver via at least one snap-fit engagement. The locking clip retains the drivers and the planetary gears in operable engagement with one another and the sun gear such that a rotational input provided to the second driver drives rotation of the inner shaft.

Abstract: A method of treating or cleaning a wound bed is disclosed. The method includes obtaining a wound-care device. The wound-care device includes a handle and a head monolithically formed with a first end of the handle and extending away from the first end of the handle. The head includes a base and a plurality of projections monolithically formed with the base and extending away from the base. During use of the wound-care device, a user may manually disturb a wound bed of a patient by placing one or more projections of the plurality of projections in contact with the wound bed and manually moving, while the one or more projections are in contact with the wound bed, the wound-care device with respect to the wound bed.

Abstract: It is disclosed an actuation mechanism and ultrasonic surgical instrument. The ultrasonic surgical instrument includes an elongated body, a clamping assembly and an actuation mechanism configured to actuate the clamping assembly. The actuation mechanism includes: a handle portion; a first trigger and a second trigger pivotally arranged on the handle portion, respectively; and a driving member configured to actuate the clamping assembly, where the clamping assembly is arranged on a distal portion of the elongated body. The first trigger is engaged with the driving member through a first link, and the second trigger is engaged with the driving member through the first link and a second link. The first trigger is movable independently with respect to the second trigger during a portion of movement of the first trigger.