Systems, devices, and methods are provided for the delivery of an implant into the prostatic urethra. Embodiments of delivery systems can include a delivery device for insertion into the patient and a proximal control device for use in controlling release of the implant from the delivery device.

The multi-material stent includes a renal portion and a bladder portion with respective, different hardness. A valve is disposed within the stent to guide liquid from the renal portion of the stent to the bladder portion of the stent. The present invention relates towards systems and method for stents. More particularly, the invention relates to a stent designed to increase patient comfort by minimizing irritation and reflux through the use of a stent that incorporates one or more flexible elements, which may involve materials with varying degrees of hardness, and a valve disposed therein.

An implantable medical device for implantation within a passageway of a patient comprises a stent including a plurality of wires, at least one of the plurality of wires having a cross-section having a first tapered point, and a covering layer having an inner diameter and an outer diameter. In some embodiments, the plurality of wires may be disposed at least partially around the covering layer. Additionally in some embodiments, the first tapered point may extend outward further than the outer diameter of the covering layer.

A dilating device for the prostatic urethra comprising: Prostatic implant includes independently actuatable distal retractor incorporating and proximal retractor. Retractors may be connected via a spine member. System and method include implant manipulator detachably connected to implant, for manipulating and forcing implant into close proximity, for delivery into subject.

A urinary prosthesis can include an elongate tube that can extend from outside a patient's body, through the patient's urethra, and into the patient's bladder. A funnel can be coupled to a terminal end portion of the elongate tube, and can be positioned inside the patient's bladder so that a surface of the funnel contacts tissue within the patient's bladder surrounding the patient's urethra across a full 360 contact profile.

Methods are provided for the delivery of an implant into a body lumen of a patient. The method includes the steps of advancing a delivery device that includes a first tubular member housing an implant, a distal control member slidable within the first tubular member and releasably coupled with a distal portion of the implant, and an elongate grasper member slidable within the first tubular member and releasably coupled with a proximal portion of the implant. The method includes causing relative motion between the elongate grasper member and the first tubular member to expose at least a portion of the implant within the first tubular member, and then releasing the distal portion of the implant from the distal control member and the proximal portion of the implant from the elongate grasper member.

Disclosed is a bending-resistant nerve catheter and a preparation method and application thereof, and relates to the technical field of tissue engineering materials. The catheter of the present application includes an inner layer, a middle layer and an outer layer, and each layer uses raw materials of biodegradable polymers; among them, the inner layer includes a smooth surface inner layer, an oriented microchannel inner layer or a fibrous inner layer, the middle layer is a fibrous middle layer with crossing angles, the middle layer is prepared by entangling micron fibers with a certain angular arrangement, and the outer layer is made of randomly entangled polymer fibers and is tightly bonded to the middle layer.

An example medical stent for treating a body lumen is disclosed. The example stent includes an expandable scaffold having a first end region, a second end region and an outer surface. The stent further includes a first fixation member coupled to the expandable scaffold and a biodegradable material disposed along the first fixation member at a first tissue engagement region. Further, the biodegradable material is designed to degrade from a first configuration in which the biodegradable material shields the first fixation member from a target tissue site to a second configuration in which the first fixation member is engaged with the target tissue site.

A balloon including an outer circumferential portion which dilates to form a hollow circular cross-section and deflates when the internal pressure is reduced, an inner circumferential portion positioned inside the outer circumferential portion, and support portions positioned between the outer circumferential portion and the inner circumferential portion to support deflating the outer circumferential portion while compressing the outer circumferential portion. The support portions form first compression portions, which have a high compressive strain, and second compression portions, which have a compressive strain lower than the first compression portions. When the outer circumferential portion deflates, the distance between the center of the circular cross-section and the maximum outer diameter portion becomes shorter than the radius of the circular cross-section formed when a minimum pressure, which is necessary for dilating the outer circumferential portion to have a circular cross-section, is applied to the outer circumferential portion.

Systems, instruments, methods, and compositions are described involving removing a portion of the epidermis within a donor site on a subject, and harvesting dermal plugs within the donor site. An injectable filler is formed by mincing the dermal plugs. The injectable filler is configured for injecting into a recipient site on the subject.