Abstract: A medical device includes a handle, a shaft extending from the handle, and an articulation member integral with or attached to a distal end of the shaft. The articulation member includes a first portion coupled to a second portion, the second portion is receivable in a slot defined by the first portion, and the handle is coupled to each of the first portion and the second portion and to articulate the first portion independently of articulating the second portion.

Abstract: A medical device, for example a delivery catheter, may include a handle portion, a shaft portion extending distally from the handle portion, a deployment mechanism, and an actuation member positioned on the handle portion. The shaft portion may include a working channel and a distal tip portion having a payload chamber configured to receive a payload, such as a bio-absorbable foam. The distal tip portion may be operatively connected to the working channel. The deployment mechanism may be positioned in the working channel, and may be operable to deploy the payload out from the distal tip portion. The actuation member may be actuatable to operate the deployment mechanism.

Abstract: A medical device may include a handle and an end cap. The handle may include a first movable body and a stationary body. The end cap may include an outer portion, an inner portion disposed within the outer portion, and at least one biasing member. The outer portion may define a receptacle configured to contain a material. The inner portion may be proximal to the receptacle, within the outer portion, and coupled to the first movable body by at least one control element. The biasing member(s) may be disposed between a proximal face of the inner portion and a distal face of a proximal wall of the outer portion. Accordingly, movement of the first movable body relative to the stationary body moves the inner portion relative to the outer portion. Movement of the inner portion may be configured to deliver the material.

Abstract: A medical device may comprise a handle having a fluid source, a conduit coupled to the handle, and a distal portion coupled to a distal end of the conduit. The distal portion may comprise an outer portion defining a lumen and an inner portion. The inner portion may be disposed within the lumen if the outer portion. The inner portion may define a cavity having a distal opening. The cavity may be configured to contain a material. In a first configuration of the distal portion, the material is disposed within the inner portion. Delivery of a fluid from the fluid source into the lumen of the outer portion transitions the distal portion from the first configuration to a second configuration and causes the inner portion to move distally relative to the outer portion and deliver at least a portion of the material.

Abstract: A device includes a flexible sheath, a member, an expansion device, and a therapeutic patch. The sheath has a length selected to extend from a distal end which, when the device is in operative configuration, is adjacent to the target site, to a proximal end. The member extends through the sheath from a proximal end to a distal end. The expansion device is coupled to and extends distally from a distal end of the member. The patch is wrapped around the expansion device and forced radially outward into contact with and adhere to a first target portion of tissue when the expansion device is moved to deployed configuration. The expansion device is movable, after the patch has been adhered to the portion as desired, from deployed configuration to insertion configuration to separate the patch from the expansion device leaving the patch in a desired position adhered to the portion.

Abstract: A medical device may comprise: a handle including an actuator, an end container configured to be coupled to a distal end of another medical device, the end container including a cavity including a movable portion, at least one channel, and a distal opening; a control element coupling the actuator to the movable portion of the end container. A proximal movement of the actuator may move the movable portion of the end container proximally within the cavity of the end container. The cavity may be configured to hold a fluid, and the proximal movement of the movable portion is configured to apply a compressive force to the fluid so that the fluid is expelled distally through the distal opening.

Abstract: A medical device includes a handle, a shaft extending from the handle, and an articulation member integral with or attached to a distal end of the shaft. The articulation member includes a first portion coupled to a second portion, the second portion is receivable in a slot defined by the first portion, and the handle is coupled to each of the first portion and the second portion and to articulate the first portion independently of articulating the second portion.

Abstract: A medical device includes a handle including a first slot, a first control device movable within the first slot in a proximal direction and a distal direction, and a sheath extending from the handle and having a longitudinal axis, the sheath defining a first lumen extending from the handle to a distal end of the sheath. A first tube extends within the first lumen, the first tube is connected to the first control device and moves between a first position, where a distalmost end of the first tube is flush with or proximal of a distalmost end of the sheath, and a second position, where the distalmost end of the first tube is positioned distal of the distalmost end of the sheath. The first slot extends parallel to the longitudinal direction of the sheath.

Abstract: A medical device that includes a handle, a shaft extending distally from the handle, an end effector extending distally from the shaft, a first actuator movably coupled to the handle, and a second actuator movably coupled to the handle. The first actuator is configured to (1) articulate the shaft in response to translating the first actuator in a first direction relative to the handle and the second actuator, and (2) actuate the end effector in response to translating the first actuator in a second direction relative to the handle and the second actuator. The second actuator is configured to (1) articulate the shaft in response to translating the second actuator in the first direction relative to the handle and the first actuator, and (2) actuate the end effector in response to translating the second actuator in the second direction relative to the handle and the first actuator.

Abstract: A biopsy forceps device includes a control member; a yoke coupled to the member; jaws coupled to the yoke; and a capsule. In an open configuration, the jaws are separated to receive target tissue. In a closed configuration, cutting edges of the jaws are moved toward one another to cut tissue. The capsule slidably receives the yoke and a portion of the jaws. The jaws are constrained to the closed configuration when withdrawn proximally to a first position within the capsule. When the jaws are moved to a second position, portions of the jaws are freed from the constraint capsule and spread apart. When the yoke and the jaws are moved distally and the jaws move to the open configuration, a tissue contacting structure of the yoke extends distally to engage tissue between the jaws to anchor the engaged tissue again lateral movement as the jaws contact the tissue.

Abstract: A delivery device comprises a tube having a proximal end, a distal end, and a lumen extending from the proximal to the distal end. The proximal end is mountable to a distal tip of a medical device via the lumen. The tube includes an inner wall defining the lumen, an outer wall coupled to the inner wall at the proximal and distal ends, a cavity formed from the coupled inner and outer walls and configured to hold a deliverable substance, and a plurality of openings connected to the cavity and positioned on a distal-facing surface of the distal end. At least a portion of the inner wall or the outer wall is a flexible wall that transitions between a first and a second configuration to cause delivery of the deliverable substance from the cavity to a treatment site through the openings when a force is applied to the flexible wall.

Abstract: A medical device, for example a delivery catheter, may include a handle portion, a shaft portion extending distally from the handle portion, a deployment mechanism, and an actuation member positioned on the handle portion. The shaft portion may include a working channel and a distal tip portion having a payload chamber configured to receive a payload, such as a bio-absorbable foam. The distal tip portion may be operatively connected to the working channel. The deployment mechanism may be positioned in the working channel, and may be operable to deploy the payload out from the distal tip portion. The actuation member may be actuatable to operate the deployment mechanism.

Abstract: A medical device may include a handle including a fixed body and a movable body. The movable body may be movable relative to the fixed body. The medical device may include a shaft extending from the fixed body and an end effector at a distal end of the shaft. Rotation of the movable body relative to the fixed body may permit rotation of the end effector relative to the shaft, and rotation of the movable body with rotation of the fixed body may permit rotation of the end effector with the shaft. Deflection of the movable body relative to the fixed body may permit deflection of the end effector relative to the fixed body.

Abstract: A medical device that includes a handle including a plurality of actuators. The handle defines a longitudinal axis extending through a distal end of the handle. The device includes a shaft extending from the handle and an end effector at a distal end of the shaft. A first actuator of the plurality of actuators is configured to actuate the end effector in response to translation of the first actuator relative to the handle along an axis parallel to the longitudinal axis. A second actuator of the plurality of actuators is configured to deflect the end effector relative to the shaft in response to pivoting the second actuator about an axis transverse to the longitudinal axis. A third actuator of the plurality of actuators is configured to rotate the end effector relative to the shaft in response to rotation of the third actuator relative to the handle about the longitudinal axis.

Abstract: A medical device comprising a handle including a handle body and an actuator, and a shaft extending distally from the handle body, wherein the shaft comprises of a shape memory material, wherein the shaft includes a proximal section and a distal section, the proximal section having a first austenitic finish temperature and the distal section having a second austenitic finish temperature, and wherein the first austenitic finish temperature is lower than the second austenitic finish temperature.

Abstract: A medical device that includes a handle, a shaft extending distally from the handle, an end effector extending distally from the shaft, a first actuator movably coupled to the handle, and a second actuator movably coupled to the handle. The first actuator is configured to (1) articulate the shaft in response to translating the first actuator in a first direction relative to the handle and the second actuator, and (2) actuate the end effector in response to translating the first actuator in a second direction relative to the handle and the second actuator. The second actuator is configured to (1) articulate the shaft in response to translating the second actuator in the first direction relative to the handle and the first actuator, and (2) actuate the end effector in response to translating the second actuator in the second direction relative to the handle and the first actuator.

Abstract: A clipping system includes an adapter configured to be mounted over an insertion device and a clip including first and second jaws movable between an insertion configuration and an initial deployed configuration. A first extending member is releasably coupled to the clip and movably connected to the adapter to permit a movement of the clip relative to the adapter from the insertion configuration to the initial deployed configuration. The first extending member is configured to permit withdrawal of the adapter away from the clip to place the system in a review configuration to enhance a visual observation of the clip. The first extending member is operable to retract the clip over the adapter so that the clip is forced open, freeing the clip from tissue on which it has been clipped. The first extending member is configured to release the clip therefrom in a final deployed configuration.

Abstract: An assembly of a medical delivery device includes an inner sleeve including a flange at a proximal end. The flange includes one or more through holes. The assembly also includes an outer sleeve movably coupled to the inner sleeve. A distal tip of the outer sleeve includes a plurality of openings for delivering an adhesive to a treatment site. The assembly further includes a cavity formed between the inner sleeve and the outer sleeve and configured to hold the adhesive prior to the delivering. The assembly yet further includes one or more actuators connected to a proximal end of the outer sleeve and extended via the one or more through holes to a handle of the medical delivery device. Actuation of the one or more actuators moves one of the inner sleeve or the outer sleeve relative to the other to cause the delivering of the adhesive.

Abstract: A medical device may comprise a handle, wherein the handle includes a movable body and a main body; a cap configured to be coupled to a distal end of a scope; a patch, wherein the patch is moveable relative to the cap; and a petal body. The patch may be removably coupled to the petal body. The medical device may further comprise an actuator body coupling the patch to the moveable body such that movement of the moveable body extends the patch from the cap. The petal body may be configured to transition between a closed configuration in which the patch is retracted, and an open configuration in which the patch is extended radially-outward from a central longitudinal axis of the scope.

Abstract: A biopsy forceps device includes a control member; a yoke coupled to the member; jaws coupled to the yoke; and a capsule. In an open configuration, the jaws are separated to receive target tissue. In a closed configuration, cutting edges of the jaws are moved toward one another to cut tissue. The capsule slidably receives the yoke and a portion of the jaws. The jaws are constrained to the closed configuration when withdrawn proximally to a first position within the capsule. When the jaws are moved to a second position, portions of the jaws are freed from the constraint capsule and spread apart. When the yoke and the jaws are moved distally and the jaws move to the open configuration, a tissue contacting structure of the yoke extends distally to engage tissue between the jaws to anchor the engaged tissue again lateral movement as the jaws contact the tissue.