Abstract: A medical device and method for facilitating a surgery through a body opening is disclosed. The medical device includes a flexible member configured to be placed within the body opening so as to cover a portion of the body opening. The flexible member includes a distal end portion with a closed end, a proximal end portion with an open end and an elongate portion joining the proximal end portion and the distal end portion. The proximal end portion is configured to extend out of the patient's body opening to cover an area around and outside the patient's body opening.

Abstract: According to an aspect of the present invention, surgical films for soft tissue repair are provided. The surgical films comprise at least one sheet of a non-filamentous material within which pores are formed. Further aspects of the invention, among others, pertain to methods of using such surgical films and to kits containing such surgical films.

Abstract: A medical device and method for facilitating a surgery through a body opening is disclosed. The medical device includes a flexible member configured to be placed within the body opening so as to cover a portion of the body opening. The flexible member includes a distal end portion with a closed end, a proximal end portion with an open end and an elongate portion joining the proximal end portion and the distal end portion. The proximal end portion is configured to extend out of the patient's body opening to cover an area around and outside the patient's body opening.

Abstract: In one embodiment, a medical device includes a resorbable material that is configured to be disposed within the body of the patient proximate a bodily implant. The resorbable material is configured to frictionally retain the implant in place within the body of the patient for at least a period of time. In one embodiment, a kit includes an implant and a resorbable material. The implant is configured to be disposed within a body of a patient. The resorbable material is configured to be disposed within the body of the patient proximate the implant to frictionally retain the implant in place within the body of the patient for a period of time. The resorbable material is configured to be resorbed by the body after the period of time.

Abstract: In one embodiment, a medical device includes a resorbable material that is configured to be disposed within the body of the patient proximate a bodily implant. The resorbable material is configured to frictionally retain the implant in place within the body of the patient for at least a period of time. In one embodiment, a kit includes an implant and a resorbable material. The implant is configured to be disposed within a body of a patient. The resorbable material is configured to be disposed within the body of the patient proximate the implant to frictionally retain the implant in place within the body of the patient for a period of time. The resorbable material is configured to be resorbed by the body after the period of time.

Abstract: In one embodiment, a medical device includes a needle and a catch. The catch has a body portion. The body portion of the catch defines a cavity. The catch is configured to be coupled to the needle such that at least a portion of the needle is disposed within the cavity.

Abstract: A medical device including a break having a housing member and an actuation member. The housing member has a receiving portion and is configured to be removably coupled to a syringe. The actuation member is movably coupled to the housing member.

Abstract: According to one aspect of the invention, composite implants for soft tissue repair are provided which comprise (a) a substantially two-dimensional piece of biologic matrix material and (b) one or more non-absorbable synthetic polymeric filaments.

Abstract: In one embodiment, a medical device includes an elongate member, a fixation device and a driving member. The elongate member defines a lumen and includes a proximal end and a distal end. The distal end of the elongate member has an opening. The fixation device is at least partially disposed within the elongate member and includes a tissue piercing portion at a distal end of the fixation device. The driving member is at least partially disposed within the elongate member and is configured to move the fixation device from a position within the lumen to a location outside of the lumen through the opening. The opening at the distal end of the elongate member is angled to insert the fixation device in a tissue of a patient at an angle to a plane of the tissue of the patient to fasten a bodily implant to the tissue.

Abstract: Medical devices such as ureteral stents, and methods of use thereof are disclosed. The medical device may include an elongate member configured to be implanted within a patient's body, wherein the elongate member includes an outermost diameter and a plurality of support members disposed within a biodegradable matrix. Degradation of the biodegradable material may result in a reduction of size of the medical device. Some or all of the support members, such as at least two of the support members, may be arranged non-concentrically.

Abstract: Ureteral stents assembled from multiple segments and methods for using the same in body lumens are described. The ureteral stents optionally include multiple segments having different compositions or characteristics, such as radiopacity, stiffness or flexibility, and loading with therapeutic agents.

Abstract: An injection device for injecting a material into tissue may include a sheath having a distal end. The injection device may also include an injector having an outlet tube. The outlet tube may be received in the sheath, and may include a distal portion with a penetrating tip for penetrating the tissue. The sheath and the outlet tube may be slidable relative to each other, to extend a length of the distal portion from the distal end. The injection device may also include an adjuster operatively coupled to at least one of the sheath and the outlet tube. The adjuster may be configured to control relative movement between the sheath and the outlet tube for selectively adjusting the extended length.

Abstract: Systems and methods for performing medical procedures in body lumens are described. Embodiments of the methods include forming a plug to partially or fully occlude the lumen and moving the plug through a surgical field. Embodiments of the systems include an elongate body graspable by a surgical instrument or by a surgeon that are adapted to anchor to the plug.

Abstract: In an embodiment, the invention discloses a medical assembly comprising a ring shaped member configured to surround a vaginal wall and an arm member. The arm member is coupled to the ring shaped member and configured to extend from the ring shaped member to a bodily location. The arm member is configured to be coupled to the bodily location and provide a support to a vagina of a patient. The ring shaped member is configured to hold the arm member during implantation of the arm member within the body. The ring shaped member is further configured to be cut after implantation so that the ring shaped member is transformed into a non-circular shape.

Abstract: In one general aspect, an apparatus can include a mesh having an edge, a loop coupled to the edge of the mesh, and a suture coupled to at least one of the loop or the edge of the mesh, the suture having a barb. The loop can have an inner diameter smaller than a combined width of the suture and at least a portion of an outer portion of the barb.

Abstract: In one embodiment, a stent includes a retention portion and an elongate portion. The retention portion is configured to help retain the stent in place within a body of a patient. The elongate portion extends from the retention portion. The elongate portion has a sidewall defining a lumen and the outer surface of the sidewall includes a pattern. The sidewall has a first section and second section. The first section of the sidewall has a first thickness. The second section of the sidewall has a second thickens different than the first thickness.

Abstract: The resorption of a medical implant can be controlled with the use of particles embedded in a resorbable bulk material forming the implant or portion thereof. The implant can be removed from a body of a mammal by natural biological mechanisms after use. The resorption of the implant can involve swelling and/or hydrolyzing of the particles within the implant upon contact with a body fluid such that porosity and flow of fluid within the bulk material of the implant is increased. Resorption of the implant may also involve the use of particles with magnetic properties embedded within the implant such that an applied magnetic field causes the particles to vibrate within the bulk material thereby increasing the porosity and thus the flow of fluid, hence facilitating resorption of the implant. The resorption rate of the implant can be controlled by modulating swelling, hydrolysis, or movement of the embedded particles.

Abstract: In one embodiment, a medical device includes a resorbable material that is configured to be disposed within the body of the patient proximate a bodily implant. The resorbable material is configured to frictionally retain the implant in place within the body of the patient for at least a period of time. In one embodiment, a kit includes an implant and a resorbable material. The implant is configured to be disposed within a body of a patient. The resorbable material is configured to be disposed within the body of the patient proximate the implant to frictionally retain the implant in place within the body of the patient for a period of time. The resorbable material is configured to be resorbed by the body after the period of time.

Abstract: A medical device and method for facilitating a surgery through a body opening is disclosed. The medical device includes a flexible member configured to be placed within the body opening so as to cover a portion of the body opening. The flexible member includes a distal end portion with a closed end, a proximal end portion with an open end and an elongate portion joining the proximal end portion and the distal end portion. The proximal end portion is configured to extend out of the patient's body opening to cover an area around and outside the patient's body opening.

Abstract: A bodily implant is provided to support body tissues of a patient. The bodily implant includes a strip having a first portion and a second portion. The strip is configured to be stretched in a manner such that the second portion is stretched from a first length to a second length. The second portion of the strip is configured to maintain the second length. The strip is further configured to be disposed proximate to the patient's body tissues.