Abstract: A penile prosthesis includes a penile prosthetic; a pump; a reservoir; first tubing adapted to couple the penile prosthetic to the pump; second tubing adapted to couple the reservoir to the pump; and a plate adapted to couple with the penile prosthetic. The plate is implantable and adapted to orient the penile prosthetic in an anatomically natal penis position that is adapted for penetrative intercourse.

Abstract: An implant device and method is provided. The implant may be a generally spherical, hollow body having one or more layers configured to be implanted within a scrotum and a cavity sized to receive a testis. Net sheeting provides structural rigidity to the implant and facilitates suturing of the implant to the patient. The cavity has a cavity configured to permit access to the cavity. Implantation involves administering one or more anesthetic agents to a patient having at least one testis and a scrotum; cutting an at least 1.5-inch longitudinal incision in the scrotum to expose the tunica vaginalis; cutting an at least 1.5-inch longitudinal incision in the tunica vaginalis; providing the testicular implant placing the testicular implant over the at least one testis; closing the at least 1.5-inch longitudinal incision in the tunica vaginalis; connecting the testicular implant to the tunica vaginalis; and closing the scrotum.

Abstract: A pump is connected between penile cylinder(s) and a reservoir of a prosthesis. A squeezing pressure applied to the penile cylinder moves a first liquid volume out of the cylinder and into a first chamber of the pump, which displaces a piston inside of the pump. Displacement of the piston creates a vacuum space (a second chamber) between the piston and the housing of the pump, and a second liquid volume is drawn out of the reservoir and into the vacuum space. A return spring pushes the piston back to its starting position, which pushes both the first liquid volume and the second liquid volume out of the pump and into the penile cylinders.

Abstract: The invention relates to the radiation treatment of colorectal cancerous tissue in the rectum of a human or animal subject. In particular the invention relates to an endorectal probe device for effecting radiation treatment of colorectal cancerous tissue in the rectum of a human or animal subject. Furthermore the invention relates to an afterloading apparatus for effecting radiation treatment of colorectal cancerous tissue in the rectum of a human or animal subject using an endorectal probe device according to the invention. Moreover the invention relates to a method for effecting radiation treatment of colorectal cancerous tissue in the rectum of a human or animal subject, wherein the method implements the endorectal probe device according to the invention.

Abstract: An applicator for delivery of radiotherapy seeds to a tumor of a patient through an elongate needle (104). The elongate needle comprises a needle handle (204) and a needle tube having a given length for insertion into the patient. The applicator comprises an elongate applicator tube (106) designed to pass through the elongate needle, wherein the elongate applicator tube defines an internal channel which receives one or more radiotherapy seeds (110), an applicator handle (210) configured to be attached to the needle handle (204); and a stylet (108) within the elongate applicator tube. The elongate applicator tube is longer than the elongate needle.

Abstract: Stimulation devices and methods of use are described herein. An example stimulation device configured to stimulate a portion of a body of a user comprises a housing that includes a casing and a covering. The casing includes a nozzle, a motor disposed within the casing configured to generate stimulation patterns, a drive shaft connected to the motor, a sensor configured to detect changes in the rotation of the draft shaft, a controller, and a battery. The covering covers a portion of the casing.

Abstract: Systems for promoting sexual well-being in males and for treating erectile dysfunction using acoustic energy.

Abstract: Systems and methods for promoting sexual well-being in males and in some cases for treating erectile dysfunction and, more particularly, to such systems that use shock waves delivered to tissue.

Abstract: Exemplary brachytherapy applicators may include an interstitial tube having a body with a proximal end and a distal end and a central conduit extending from the distal end of the body, wherein the central conduit includes a proximal opening, a distal opening, and a channel extending from the proximal opening to the distal opening, and wherein the proximal opening is offset from an axis of the body. The proximal opening may be configured to fluidly connect to a brachytherapy guide tube, and the channel of the central conduit may be dimensioned to receive at least one of a needle or a catheter therethrough.

Abstract: The present invention is directed to a method of penile prosthesis implantation that is minimally invasive, particularly in comparison to traditional methods of penile prosthesis implantation. The implantation method utilizes image guidance and a catheter deployment system for implanting a penile prothesis into the corporal body of a penis of a patient. More specifically, the implantation method may utilize the Seldinger technique and/or a modified Seldinger technique for implanting the prothesis. The method of implantation may result in more accurate placement, better cosmetic results, faster healing, and less likelihood for infections and other complications.

Abstract: A wirelessly powered inflatable medical implant system includes a medical provider software application, a patient external controller and a MR-Conditional, nonferrous pump in reservoir implant. The medical provider software application programs the patient external controller for the patient to transmit wireless power and control signals to circuitry in a pump in reservoir implant. In response, the pump in reservoir implant, containing a fluid reservoir and pump package submerged therein, transfers fluid from the reservoir through tubing, and into one or more inflatable medical implants. Submerging the pump package within the reservoir simplifies surgery in males and pump placement in females and provides pump package heatsinking to limit implant overheating.

Abstract: A water and gas dual-purpose electric erection aid includes a vacuum barrel and a device bin, which has a seal cover that covers one end of the vacuum barrel and a pump valve pipeline mechanism arranged in the seal cover and used for vacuumizing the vacuum barrel; the device bin is installed with a button control assembly via a support frame; the seal cover is provided with an open groove exposing a button part of the button control assembly and the open groove is tightly attached to the button control assembly; the pump valve pipeline mechanism is communicated with two connection ports formed at the top of the vacuum barrel and a vent cover fixedly arranged on the seal cover through a connecting pipe. The erection aid can be used both in air and underwater. It has good adjuvant treatment and improvement effects on men suffering from sexual dysfunction.

Abstract: The present invention relates to a system comprising an apparatus for treating a sexually dysfunctional male patient. The apparatus comprises at least one implantable vibrator adapted to be implanted within at least one corpus cavernosum of a human patient, wherein said vibrator is adapted to cause vibration in at least one of the corpus cavernosum for stimulating the sexually responsive tissue of the penis. The system further comprises an operation device adapted to operate the vibrator.

Abstract: The present invention relates to a method of implanting a penile implant for curing impotence of a patient. The method provides steps of cutting a skin of the patient, dissecting an area of a corpus cavernosum of a penis of the patient, implanting the penile implant in the corpus cavernosum. The penile implant is implanted by placing a relatively short proximal portion of the penile implant in the root of the penis, placing a flexible relatively long distal portion of the penile implant such that it extends along or in the pendulous or protruding part of the penis.

Abstract: An apparatus for providing treatment to at least one tissue includes a distal balloon, a proximal balloon, and an intermediate balloon positioned between the distal balloon and the proximal balloon and inflatable independently from the distal and proximal balloons. A source lumen is positioned within at least the intermediate balloon receives a radiation source to treat target tissue adjacent the intermediate balloon.

Abstract: Provided herein are devices, systems, and methods configured to alleviate erectile dysfunction by preventing outwards blood flow away from the penis while allowing inward blood flow into the penis to aid in erection initiation, maintenance, and stamina. The geometry, configuration, flexibility, and pliability of the device enable its use on flaccid or erect penises. The penile constriction device and band enables the system to apply an adjustable compressive force on a flaccid or an erect penis.

Abstract: An implantable inflatable penile prosthesis cylinder includes an outer tube member having a longitudinal axis, an inner tube member contained within the outer tube member, and one or more tensile support members within the inner tube member. The inner tube member includes at least one inflatable chamber section, at least a portion of which is defined by a wall of the inner tube member. The one or more tensile support members extend between interior surfaces of the wall and are placed in tension when the at least one chamber section is in an inflated state.

Abstract: A medical device and method for artificial insemination are provided. The medical device has a shield and an arm secured to the shield at one end and extending outwardly from the shield. The arm is inserted into the cervical canal of a patient and the shield covers the external os of the patient. By inserting the medical device into a patient's cervical canal after insemination, a physical barrier that holds a semen sample within the cervical canal and prevents leakage from the cervical canal back into the vaginal cavity is established. The device may have a bore extending through the device for a catheter to pass through. The bore has a valve to allow passage of the catheter and prevent backflow of semen. The arm may have a circumferential bulge to help keep the device in place during use.

Abstract: The present invention relates to compositions and methods configured to deliver a stimulus (e.g., a therapeutic agent or a therapeutically beneficial signal) to a cell, tissue, organ, or organism. The stimulus is applied at least twice, and the first and second applications are separated by a rest period in which no further stimulus is actively applied. The rest period is of a duration (e.g., about 1-6 hours) sufficient to provoke an enhanced response to the second stimulus.

Abstract: Acceleration protective trousers or G-protective trousers are double-walled forming airtight compartments. The trousers include an air-permeable, tear-resistant, fire-resistant and low-stretch synthetic textile material, and the trousers are provided with compartments which can be inflated into a circular cross-section. These compartments act as muscles by two opposite edges being pulled together and the adjacent pieces of textile material being stretched. These compartments extend along the trouser legs and are connected at the upper end of the trouser legs. The compartments on the outer sides of the trouser legs extend upwards from the groins and terminate in a bag-like bladder towards the lower abdomen. On the rear side of the trousers they communicate with one another via a connecting channel. A coccyx channel branches off downwards and extends towards the crotch. The compartments communicate via at least one hose with raccord with an automatically meterable compressed air supply.