Abstract: Some embodiments are directed to medical devices, and methods for making and using the medical devices. An exemplary medical device includes a first elongate member, a second elongate member, and a coupler. The coupler may be configured to removably couple the first elongate member to the second elongate member.

Abstract: In an embodiment, the invention discloses a medical device configured to be delivered and placed within a patient's body. The medical device includes an implant and a cover member. The implant is configured to be disposed within the patient's body. The implant includes a support member, a first arm member and a second arm member, an elongated first sleeve, and an elongated second sleeve. The support member includes a crescent shaped opening.

Abstract: Some embodiments are directed to implants and methods for making and using the implants. An exemplary implant includes a first elongate member and a second elongate member each having a first end portion and a second end portion. The first and second end portions of the first elongate member may be configured to be coupled to tissue of a patient proximate the vagina and sacrum, respectively. The first elongate member may define a first opening and a second opening, where the second elongate member may be configured to extend through the first opening and the second opening. The first end portion of the second elongate member may be coupled to tissue proximate the vagina of the patient.

Abstract: According to an aspect, a medical device includes an elongate member, a first arm extending from the elongate member, a second arm extending from the elongate member, the second arm being configured to move with respect to the first arm, and a needle coupled to the elongate member, the needle being configured to move with respect to the elongate member.

Abstract: According to an aspect, a medical device includes a needle member and a handle member. The handle member is coupled to the needle member. The handle member has a substantially flat portion. The handle member defines a groove. The groove is disposed on the substantially flat portion of the handle member.

Abstract: The present invention discloses a medical assembly including an implant, a first sleeve, a second sleeve and an elongate member. The implant has a first portion, a second portion and a mid portion. The first portion of the implant is configured to be enclosed by the first sleeve and the second portion of the implant is configured to be enclosed by the second sleeve. The elongate member is configured to couple the implant with the first sleeve and the second sleeve and is configured to respectively extend from the first portion to the mid portion of the implant and past the mid portion such that the elongate member exits the implant through the mid portion and forms a loop near the mid portion.

Abstract: The present disclosure is directed to a medical device. Systems and methods are provided for removing particles, stone fragments and/or stone dust from a patient. The medical device described herein may work by positioning within the kidney, a catheter to flush stone dust. The catheter may include a dual lumen tube which provides fluid through one lumen to irrigate a target area and provides suction through a second lumen to carry out the irrigation fluid along with stone dust. This stone dust may be the result of a previously performed stone dusting. The irrigation fluid may be introduced with a pulsed flow. The pulsed flow irrigation may facilitate the removal of small stone fragments. The suction may be applied by a vacuum at to evacuate the target area at a flow rate balanced with the flow rate of the introduction of the irrigation fluid.

Abstract: An insertion device, includes an elongate member having a needle portion and a handle portion. The handle portion includes a visual indicator. The visual indicator is configured to indicate an orientation of the needle portion.

Abstract: According to an aspect, a medical device may include a needle member, and a handle coupled to the needle member. The handle may define a track portion. The medical device may also include a pusher member having a sheath disposed around a portion of the needle member, and an extension member being movably coupled to the track portion of the handle such that the pusher member is configured to move from a first position to a second position during a surgical procedure. The pusher member may be removable from the handle. The sheath may define a slot, and the pusher member may be removable from the needle member through the slot.

Abstract: Some embodiments are directed to medical devices, and methods for making and using the medical devices. An exemplary medical device includes a first elongate member, a second elongate member, and a coupler. The coupler may be configured to removably couple the first elongate member to the second elongate member.

Abstract: Some embodiments are directed to implants and methods for making and using the implants. An exemplary implant includes a first elongate member and a second elongate member each having a first end portion and a second end portion. The first and second end portions of the first elongate member may be configured to be coupled to tissue of a patient proximate the vagina and sacrum, respectively. The first elongate member may define a first opening and a second opening, where the second elongate member may be configured to extend through the first opening and the second opening. The first end portion of the second elongate member may be coupled to tissue proximate the vagina of the patient.

Abstract: A medical device assembly includes an implant having a support portion, and an arm portion and a dilator. The medical device assembly further includes a first suture having a first portion coupled to the arm portion of the implant, and a second portion coupled to the dilator. In addition, the assembly includes a second suture having a first portion coupled to the arm portion of the implant, and a second portion coupled to the dilator.

Abstract: The invention discloses an implant. The implant may include a first flap and a second flap. The first flap may further include a first portion, a second portion and a transition region. The first portion may be configured to be attached proximate a sacrum. The second portion may be configured to be attached to an anterior vaginal wall. The transition region lies between the first portion and the second portion. The second flap may be fabricated such that a portion of the second flap is configured to be attached to a posterior vaginal wall. The implant may be configured such that a value corresponding to a biomechanical parameter defining a biomechanical attribute of the portion of the first flap attaching to the anterior wall is different from a value of the biomechanical parameter defining the biomechanical attribute of the portion of the second flap attaching to the posterior wall.

Abstract: In an embodiment, the invention discloses a medical device configured to be delivered and placed within a patient's body. The medical device includes an implant and a cover member. The implant is configured to be disposed within the patient's body. The implant includes a support member, a first arm member and a second arm member, an elongated first sleeve, and an elongated second sleeve. The support member includes a crescent shaped opening.

Abstract: The invention discloses an implant. The implant may include a first flap and a second flap. The first flap may further include a first portion, a second portion and a transition region. The first portion may be configured to be attached proximate a sacrum. The second portion may be configured to be attached to an anterior vaginal wall. The transition region lies between the first portion and the second portion. The second flap may be fabricated such that a portion of the second flap is configured to be attached to a posterior vaginal wall. The implant may be configured such that a value corresponding to a biomechanical parameter defining a biomechanical attribute of the portion of the first flap attaching to the anterior wall is different from a value of the biomechanical parameter defining the biomechanical attribute of the portion of the second flap attaching to the posterior wall.

Abstract: In one embodiment, a medical device includes a tissue anchor has a first portion and a second portion. The tissue anchor is configured to be placed within bodily tissue of a patient. The first portion of the tissue anchor includes an extension member configured to engage the bodily tissue to help retain the tissue anchor within the bodily tissue. The first portion has an inner surface and defines a cavity. The second portion of the tissue anchor has a helical ridge. The helical ridge is configured to engage the inner surface of the first portion of the tissue anchor to movably couple the second portion of the tissue anchor to the first portion of the tissue anchor.

Abstract: The present invention discloses a medical assembly including an implant, a first sleeve, a second sleeve and an elongate member. The implant has a first portion, a second portion and a mid portion. The first portion of the implant is configured to be enclosed by the first sleeve and the second portion of the implant is configured to be enclosed by the second sleeve. The elongate member is configured to couple the implant with the first sleeve and the second sleeve and is configured to respectively extend from the first portion to the mid portion of the implant and past the mid portion such that the elongate member exits the implant through the mid portion and forms a loop near the mid portion.

Abstract: A thin-walled polymeric component that may have a selected complex shape, and a method of forming the component. The method includes heating a portion of a polymeric film to a selected malleable temperature, and forming a protrusion in the heated portion while it is malleable. The protrusion defines a protrusion having a first shape. The method also includes positioning a forming tool in the protrusion's interior and drawing a partial vacuum from within the protrusion so as to exert a force on the protrusion and move the protrusion's sidewalls inwardly into engagement with the forming tool. As the partial vacuum is drawn, the protrusion moves to a second shape that may be different than the first shape and that closely conforms to the selected shape of the forming tool. The protrusion is cooled below the malleable temperature and the forming tool is then removed.

Abstract: A thin-walled polymeric component that may have a selected complex shape, and a method of forming the component. The method includes heating a portion of a polymeric film to a selected malleable temperature, and forming a protrusion in the heated portion while it is malleable. The protrusion defines a protrusion having a first shape. The method also includes positioning a forming tool in the protrusion's interior and drawing a partial vacuum from within the protrusion so as to exert a force on the protrusion and move the protrusion's sidewalls inwardly into engagement with the forming tool. As the partial vacuum is drawn, the protrusion moves to a second shape that may be different than the first shape and that closely conforms to the selected shape of the forming tool. The protrusion is cooled below the malleable temperature and the forming tool is then removed.

Abstract: A thin-walled polymeric component that may have a selected complex shape, and a method of forming the component. The method includes heating a portion of a polymeric film to a selected malleable temperature, and forming a protrusion in the heated portion while it is malleable. The protrusion defines a protrusion having a first shape. The method also includes positioning a forming tool in the protrusion's interior and drawing a partial vacuum from within the protrusion so as to exert a force on the protrusion and move the protrusion's sidewalls inwardly into engagement with the forming tool. As the partial vacuum is drawn, the protrusion moves to a second shape that may be different than the first shape and that closely conforms to the selected shape of the forming tool. The protrusion is cooled below the malleable temperature and the forming tool is then removed.