Abstract: Various embodiments disclosed relate to a balloon catheter for use with a ureteroscope. A balloon catheter may include an elongated shaft having a proximal end and a distal end, the elongated shaft shaped for insertion into a patient. A balloon catheter may include a balloon attached at the distal end of the elongated shaft, wherein the balloon is inflatable between a collapsed state and inflated state, and wherein a wall of the balloon comprises a balloon wall material defining plurality of valves that open to allow fluid flow therethrough when the balloon is in the inflated state.

Abstract: A biliary diagnostic device comprises a tubular body comprising an outer wall and an internal lumen, and a biliary diagnostic sensor comprising for analyzing biological matter in contact with the tubular body. A method of guiding an endoscope to a bile duct comprises inserting the endoscope into a duodenum, engaging a sensor with biological matter, electrically analyzing biological matter with the sensor to identify an electrical parameter, identifying liver bile in the biological matter from the electrical parameter, and guiding the endoscope through the duodenum based on the bile. A method of identifying biological matter comprises engaging a medical device sensor with biological matter in a bile duct, electrically analyzing biological matter with the sensor to identify an electrical parameter, identifying biological matter from a liver, pancreas or gall bladder from the electrical parameter, and outputting indicia of the biological matter to a user of the medical device.

Abstract: A medical device for debridement can include an elongate housing, a shaft extending through the housing and distally therefrom, a drive to manipulate the cutter, and a collapsible handle than can to couple with the housing. An elongate grip of the handle can turn aft and be at least partially disposed in the elongate housing for use of the device with pen grip. The elongate grip of the handle can turn fore and extend distally from the housing for use of the device with pistol grip.

Abstract: A method includes: delivering a biodegradable expandable member into a body cavity of a patient; insufflating the biodegradable expandable member in the body cavity to expand the body cavity; sealing the biodegradable expandable member against an inner wall of the body cavity to seal the body cavity internally; and delivering an endoscope into the body cavity.

Abstract: A laser lithotripsy guide system for guiding a laser fiber during a lithotripsy procedure may include a guide which may include a proximal end portion and a distal end portion. The guide may define a guide bore to receive a laser fiber therethrough. The guide may include at least one prong on the distal end portion. The guide system may also include a mounting assembly which may be securable to the laser fiber. The mounting assembly may be releasably insertable into the proximal end portion of the guide to releasably secure the mounting assembly to the guide.

Abstract: A medical device can include an elongate member, an irrigation port at a proximal end of the elongate member, and a resection assembly. The elongate member defines a first track and a second track. The resection assembly extends from a distal end of the elongate member and has a first member, a second member, and an electrically activatable resection element extending from a distal end of the first member. The first member includes a first portion located along the first track. The second member has a first portion located along the second track and the second member includes a longitudinally axial fluid conduit passageway. The passageway is in fluid communication with the irrigation port.

Abstract: A sizing device configured to measure a dimension of a lumen in a patient can include an elongated member, an extendable assembly, and an actuation mechanism. The elongated member can be insertable into the patient and define a lumen extending from a proximal end to a distal end. The extendable assembly can be insertable into the lumen. The extendable assembly can include elements that can have a shape-set memory bias. The shape-set memory bias can be configured to allow the elements to extend radially outward from a central axis of the elongated member. The actuation mechanism can be operably coupled to the extendable assembly and can be configured to move the elements between a retracted position and a plurality of deployed positions.

Abstract: A medical device can include an elongate outer member and an elongate inner member in the elongate outer member. The elongate outer member defines a first lumen and includes a lateral suction port that is in fluid communication with the first lumen. The elongate inner member is rotatable relative to the elongate outer member and defines a second lumen. The second lumen includes an opening at a distal end of the elongate inner member to allow passage of fluid into the second lumen. The elongate inner member has a first lateral passage where the first lateral passage is rotatable into partial alignment with the lateral suction port to provide or control suction or other fluid communication between the lateral suction port and the second lumen. The medical device also has an electrode at a distal end of the inner member.

Abstract: Disclosed herein is a fluid management assembly. The fluid management assembly includes a handpiece, a slider based fluid control mechanism, and a fluid occluding member. The slider based fluid control mechanism housed in the handpiece. The fluid occluding member is configured to be in communication with the fluid control mechanism. The fluid occluding member being separate from the handpiece.

Abstract: A medical device includes an outer tubular member, a middle tubular member received within the outer tubular member, an inner tubular member received within the middle tubular member, and an engagement gear, wherein the inner tubular member is configured to be rotatable in one direction while the middle tubular member is configured to be simultaneously rotatable in an opposite direction through the engagement gear while the outer tubular member is configured to be stationary relative to both the middle tubular member and the inner tubular member.

Abstract: A suturing system for a scope having a scope shaft comprises a drive shaft to extend along the scope shaft, a mounting ring to mount to a distal end of the scope shaft to receive the drive shaft, a pinion gear mounted to a distal end of the drive shaft, a ring gear rotatably mounted to the mounting ring in engagement with the pinion gear, and a needle mounted to the ring gear.

Abstract: A medical device can include an elongate member that defines a lumen and a resection element that extends through the elongate member lumen. The elongate member can include a side window at a distal portion and a front window at a distal end of the elongate member and proximate to the side window. The front window can define an opening at the elongate member distal end. The resection element can be movable within the elongate member lumen where a distal end of the resection element can be exposed at the front window. The resection element can have a side window that is alignable with the elongate member side window. In addition, the resection element can define an electrically active electrode and the elongate member can define a return electrode.

Abstract: An electrosurgical device is provided. The electrosurgical device can include an elongated member configured to be attached to an elongated shaft of an endoscope, the elongated member including a distal portion that, when axially extended beyond a distal end of the shaft, bends toward a longitudinal axis of the shaft. The electrosurgical device can include an electrode exposed at the distal portion of the elongated member. The electrosurgical device can include an electrical interconnect coupling the electrode to an electrosurgical energy connection at a proximal portion of the elongated member.

Abstract: A tissue removal device, and methods of using the same, are described. An exemplary detachable, handheld tissue removal device comprises a hand piece and a blade assembly removably attachable to the hand piece. The blade assembly includes a rotatable resection member driven to rotate and surgically remove tissue from a target tissue site, and a coupling assembly including a locking member to detachably couple the blade assembly to the hand piece and operatively enable or disable the rotation of the blade assembly relative to the hand piece. The rotation of the blade assembly causes a change in rotating angle of the blade assembly. The coupling assembly can secure the rotating angle of the blade assembly during the tissue resection procedure.

Abstract: A device having a hub assembly and a lever coupled with the hub assembly is provided. The device includes a sheath coupled with the lever and extending from the hub assembly. The sheath has a surgical elevator with a surgical elevator edge along with a hypotube having an access hole. The device has a shaver blade assembly with an outer shaft having an outer blade and an inner blade within the outer blade. The outer shaft has a stop and an access hole near the outer and inner blades. The sheath partially surrounds the outer shaft and the lever moves between a first position and a second position. In the first position, the surgical elevator edge abuts the outer shaft stop and the outer shaft access hole aligns with the hypotube access hole. In the second position, the surgical elevator edge is spaced apart from the outer shaft stop.

Abstract: An endoscope may include an expandable and collapsible working channel, a flexible endoscope body, and an optical sensor located at a distal tip of the endoscope body. The optical sensor can provide a distal field of view from the distal tip. In the collapsed configuration, the working channel can be collapsed such that a channel wall is in a first position relative to the endoscope body and the working channel defines a first cross-sectional area. In the expanded configuration, the channel wall is displaced relative to the first position and the working channel defines a second cross-sectional area that is larger than the first cross-sectional area.

Abstract: A method for delivering surgical material comprises inserting a delivery device into an anatomic area, coupling a surgical material delivery system to the delivery device, the surgical material delivery system having a reservoir of surgical material, positioning an anatomic electrode relative to the anatomic area, applying a first charge to the anatomic electrode, dispensing surgical material from the delivery device, applying a second charge to surgical material leaving the delivery device opposite the first charge, and delivering charged surgical material to the anatomic area proximate the anatomic electrode via a directional-oriented electrostatic field.

Abstract: An endoscope can comprise a proximal section, an insertion section extending longitudinally from the proximal section and comprising an elongate tubular body disposed along an insertion section longitudinal axis and a lumen extending through the elongate tubular body, and a distal section extending from the insertion section and comprising an elevator portion comprising an elevator configured to position and orient one or more endotherapy tools extending from the lumen, and a camera module comprising an illumination unit and an imaging unit. The camera module can be positioned longitudinally spaced apart from the elevator portion in an in-line configuration, such that the insertion tube longitudinal axis passes through the elevator portion and the camera module. The camera module can be user-detachable from the elevator portion. The camera module can be cleaned and sanitized for reuse and the insertion section can be disposable.

Abstract: An assembly can include a first component having at least one drainage channel and at least one fluid channel. The assembly can also include a second component having at least one drainage channel and at least one fluid channel. The assembly can also include a quick-connect coupling. The quick-connect coupling can be configured to couple the first component and the second component, fluidically connect the at least one drainage channel of the first component to the at least one drainage channel of the second component, and fluidically connect the at least one fluid channel of the first component to the at least one fluid channel of the second component.

Abstract: An endoscope can comprise a proximal section, an insertion section extending longitudinally from the proximal section and comprising an elongate tubular body disposed along an insertion section longitudinal axis and a lumen extending through the elongate tubular body, and a distal section extending from the insertion section and comprising an elevator portion comprising an elevator configured to position and orient one or more endotherapy tools extending from the lumen, and a camera module comprising an illumination unit and an imaging unit. The camera module can be positioned longitudinally spaced apart from the elevator portion in an in-line configuration, such that the insertion tube longitudinal axis passes through the elevator portion and the camera module. The camera module can be user-detachable from the elevator portion. The camera module can be cleaned and sanitized for reuse and the insertion section can be disposable.