214results about "Penis implants" patented technology

A device for treatment of mitral annulus dilation is disclosed, wherein the device comprises two states. In a first of these states the device is insertable into the coronary sinus and has a shape of the coronary sinus. When positioned in the coronary sinus, the device is transferable to the second state assuming a reduced radius of curvature, whereby the radius of curvature of the coronary sinus and the radius of curvature as well as the circumference of the mitral annulus is reduced.

Described is an adjustable device for sizing a heart valve annulus by a minimally invasive route, the device comprising: a cannula comprising a proximal end, a distal end and an interior lumen; and at least one wire extending through the interior lumen of the cannula, wherein the at least one wire may be advanced or retracted through the lumen and from the distal end of the cannula, such that a segment of the wire may form a plurality of different predetermined shapes of predetermined sizes used to size the heart valve annulus. Additionally, methods of using such adjustable sizing devices are disclosed.

An implant for use in a human or animal body can include a flexible housing with an outer wall and having a chamber therein. The implant can have at least one high vapor pressure medium within the chamber. The at one high vapor pressure medium can have a combined vapor pressure equal to or greater than about the average value of the hydrostatic pressure of the implantation site plus the skin tension of the housing minus the gas tension of the dissolved gasses present at the implantation site.

A medical device and a method for providing a change of shape in a part of the body of an organism. The device is insertable into the body of the organism and comprises a member having a preferred state of shape and having a tendency to transfer its shape towards said preferred state of shape when being in a non-preferred state of shape. The device further comprises a resorbable means which is arranged to hold the member in the non-preferred state of shape and to delay the transfer when the device is inserted into the body of the organism by counteracting said transfer during resorption of the resorbable means by the surrounding body of the organism.

A device for reshaping a cardiac valve (26), which is elongate and has such dimensions as to be insertable into a cardiac vessel (24). The device has two states, in a first state (K) of which the device has a shape that is adaptable to the shape of the vessel (24), and to the second state (k′) of which the device is transferable from said first state (K). Further, the device comprises a fixing means (22,23;22a,23a) for fixing the ends of the device within the vessel (24), when the device is first positioned therein, a shape-changing member (20;20a) for transferring the device to the second state (K′) by reshaping it, and a delay means (21;21a) for delaying said reshaping until the fixing of the ends of the device has been reinforced by keeping said device in said first state (K) until the delay means (21;21a) is resorbed.

A male impotence prosthesis apparatus comprises an operable penile prosthesis implanted in an impotent patient's corpus cavernosum to provide flaccid or erect states of the patient's penis. An energy transmission device for wireless transmission of energy from outside the patient's body to inside the patient's body is provided for use in connection with the operation of the penile prosthesis.

A device for treatment of mitral annulus dilation is disclosed, wherein the device comprises two states. In a first of these states the device is insertable into the coronary sinus and has a shape of the coronary sinus. When positioned in the coronary sinus, the device is transferable to the second state assuming a reduced radius of curvature, whereby the radius of curvature of the coronary sinus and the radius of curvature as well as the circumference of the mitral annulus is reduced.

A therapeutic prosthetic device for women or men configured to transmit tactile sensations through a stimulation material to the surface of a sex organ such as the vagina or penis. The therapeutic prosthetic device can include sensors and stimulators on the outer surface and inner surface and a controller. Sensors for detecting state, sensation or movement can be disposed within, on, or separate from the device and can transmit signals electrically or wirelessly to a microprocessor, which is programmed to generate stimulation sensations in response to signals from the sensors, stimulation materials, or controllers that are transmitted to the stimulation material. In one embodiment the therapeutic prosthetic device is a therapeutic condom.

A surgically implantable device is a single unit comprised of a hydraulically activated extendable cavernosal component and a manually controlled fluid transfer system composed of a pump. Flow from the pump is directed by a one way valve interposed between a bypass from an included elastic reservoir, the pump and a second one way valve interposed between the pump and the cavernosal unit. A manually controlled release valve, interposed between the outlet of the cavernosal unit and the reservoir, permits de-activation of the cavernosal unit and returns fluid to the reservoir. These components are housed by a molded tailpiece which stabilizes the device against the symphysis pubis, positions the cavernosal implant properly within the shaft of the penis and presents the controls for easy access. An access port permits adjustment of the fluid volume. The unit has utility as a tissue expander and penile re-construction in event of congenital or traumatic deformity.

A device and method for male impotence correction and female anorgasmy. An electronic stimulator with at least one pulse generator is implanted inside the body. At least one electrode is installed in the epidural space in the sacrum section of the spinal column and a conductor running under the user's skin electrically connects the electrode to the pulse generator. The stimulator is programmable and may be controlled from outside the body. Upon command initiated by the user or the user's lover the stimulator produces very short low-voltage electrical pulses in the sacrum section that are picked up by the nerves leading to the sex organs of the user, which stimulates arousal in the user's reproductive systems. The pulses are similar to the pulses generated by heart pacemakers. In other preferred embodiments the stimulator includes one or two drug chambers and a tube extending from each chamber to a nerve for producing stimulation of a sex organ. The present invention works on both males and females. In a preferred embodiment, the programmable electronic stimulator is implanted under the skin in the patient's back. Stimulation of the nerves coming out from the parasympathetic part of the spinal cord causes dilatation of the penile arteries in the male and in the clitoris arteries of the female, which results in an erection in the male and pre-orgasmic sensation in the female. In female, the stimulation of the sacral part of the spinal cord increases sexual desire and escalation to the level of orgasm. A preferred embodiment provides for emission stimulation. Emission is stimulated by electrical excitation of the sacral part of the spinal cord by increasing the voltage of the previous impulses. The device may be preprogrammed to set in motion the emission and ejaculation process at a predetermined time interval after the start of the erection process.

A penile prosthesis is provided, which includes a generally cylindrical body portion comprising a cavity with an inner wall, a proximal end, a distal end, and at least one volume-displacing member occupying at least a portion of the cavity, wherein the at least one volume-displacing member is smaller in at least one dimension than the dimensions of the cavity to provide an internal chamber at least partially surrounding the at least one volume-displacing member and adjacent to the inner wall of the cavity. The prosthesis further includes a fluid transfer tube extending from the body portion for transferring fluid to and from the internal chamber, wherein the device is convertible from a flaccid condition to a rigid condition when a sufficient volume of fluid is transferred into the internal chamber to substantially fill the internal chamber.

An antibiotic delivery system including an intramedullary stem that is adapted to be removably mounted into a medullary canal of a bone. The stem includes a body having an inlet adapted to be in fluid communication with a source of liquid-borne antibiotic and a plurality of outlets disposed along the stem. A channel extends between the inlet and the plurality of outlets for delivering a fluid-borne antibiotic from the inlet to the plurality of outlets so as to distribute the antibiotic along the medullary canal in a controlled fashion. A method of treating an infected joint during a two-stage re-implantation of an orthopedic implant is also disclosed.

Methods and systems for detecting wall breach in inflatable prostheses rely on intrusion of a body fluid or inflation medium to electrically alter a signaling circuit. In one embodiment, an open portion of a circuit is closed to enable or modify a transmitted signal. In another embodiment, electrical current is generated to power an electrical transmission.

An implantable pump with a plurality of protrusions and grooves is described.

A male sexual impotence treatment apparatus includes an elongate adjustable constriction member extending in a loop around a male patient's penile tissue or the prolongation thereof. An adjustment device adjusts the longitudinal extension of the constriction member in the loop to temporarily constrict the penile tissue or the prolongation thereof to restrict the penile exit blood flow to achieve erection. A layer of a soft viscoelastic material is applied on the constriction member such that it is located between the constriction member and the patient's penile tissue or the prolongation thereof at least along a portion of the constriction member to protect the penile tissue or the prolongation thereof from being eroded by the constriction member. The layer has an inwardly directed radial extension in the loop such that, when the adjustment device is operated to decrease the longitudinal extension of the constriction member in the loop, the soft layer is forced to expand radially inwardly in the loop causing a corresponding increased constriction of the penile tissue or the prolongation thereof.

A penile prosthesis is provided, which includes a generally cylindrical body portion comprising a cavity with an inner wall, a proximal end, a distal end, and at least one volume-displacing member occupying at least a portion of the cavity, wherein the at least one volume-displacing member is smaller in at least one dimension than the dimensions of the cavity to provide an internal chamber at least partially surrounding the at least one volume-displacing member and adjacent to the inner wall of the cavity. The prosthesis further includes a fluid transfer tube extending from the body portion for transferring fluid to and from the internal chamber, wherein the device is convertible from a flaccid condition to a rigid condition when a sufficient volume of fluid is transferred into the internal chamber to substantially fill the internal chamber.

A pump assembly for a penile implant is provided having a mechanism which prevents spontaneous inflation of the cylinders implanted within the user. The preventative mechanism uses overpressure generated by the reservoir during unintentional compression to effectively seal the pump assembly from unintended fluid flow. The prevention mechanism itself creates all necessary forces to prevent the undesired fluid flow to the cylinders. This is accomplished by incorporating appropriate mechanisms within the pump itself.

Methods and systems for detecting wall breach in inflatable prostheses rely on intrusion of a body fluid or inflation medium to electrically alter a signaling circuit. In one embodiment, an open portion of a circuit is closed to enable or modify a transmitted signal. In another embodiment, electrical current is generated to power an electrical transmission.

A penile prosthesis is provided, which includes at least one cylinder, a reservoir, and a pump including a pump housing, at least one reservoir channel fluidly coupling the pump housing to the reservoir, at least one cylinder tube fluidly connecting the pump housing to the cylinders, and a fluid passageway fluidly coupled to the cylinder tube and a transfer chamber. The pump further includes a first poppet and a second poppet, each of which is biased toward its respective valve seat within the fluid passageway. A bypass chamber is fluidly connected to the fluid passageway by a bypass input channel and a bypass output channel. The bypass chamber comprises a bypass check valve biased toward a closed position. The pump also includes a pump bulb fluidly connected to the fluid passageway between the bypass input channel and bypass output channel along the length of the fluid passageway.

A male sexual impotence treatment apparatus comprises a constriction device implanted in an impotent male patient and engaging the patient's penile tissue. The constriction device includes an elongate adjustable constriction member extending in a loop around the penile tissue or the prolongation thereof. A connection device releasably connects the end portions of the constriction member to each other and an adjustment device adjusts the longitudinal extension of the constriction member in the loop to temporarily constrict the penile tissue or the prolongation thereof to restrict the penile exit blood flow to achieve erection. The connection device includes a female part and a male part fitting into the female part to lock them together. The design of the connection device facilitates laparoscopic surgery for implanting the constriction member.

The invention provides a sterilizable pouch having at least one wall formed of a flexible film and including an opening formed therein for providing communication to an interior space of the package. A breathable material is disposed on an outer surface of the wall covering the opening. The breathable material is joined to the outer surface of the wall with a continuous heat seal. The flexible film forming the wall comprises a multilayer film having a peel feature that permits the breathable material to be peelably removed from the surface of the pouch.

A delivery system for delivering a prosthetic heart valve to a native valve site within the human vasculature. The prosthetic valve is disposed on a balloon at the end of a balloon catheter. The balloon catheter passes through a delivery sleeve assembly and handle. A pull wire travels from the handle to a distal end of the delivery sleeve assembly. Actuation of the handle pulls on the pull wire, which causes openings in a slotted tube of the delivery sleeve assembly to close, thus causing the delivery sleeve assembly to bend. A stretchable cover is placed over the slotted tube for biasing the steerable catheter toward a straight position. Once advanced to the native valve site, the prosthetic valve is deployed by inflating the balloon.

A pump assembly for a penile implant is provided having a mechanism which prevents spontaneous inflation of the cylinders implanted within the user. The preventative mechanism uses overpressure generated by the reservoir during unintentional compression to effectively seal the pump assembly from unintended fluid flow. The prevention mechanism itself creates all necessary forces to prevent the undesired fluid flow to the cylinders. This is accomplished by incorporating appropriate mechanisms within the pump itself.

A penile prosthesis is provided, which includes at least one cylinder, a reservoir, and a pump including a pump housing, at least one reservoir channel fluidly coupling the pump housing to the reservoir, at least one cylinder tube fluidly connecting the pump housing to the cylinders, and a fluid passageway fluidly coupled to the cylinder tube and a transfer chamber. The pump also includes a pump bulb fluidly connected to the fluid passageway between the bypass input channel and bypass output channel along the length of the fluid passageway.

A stem of an artificial hip joint is capable of removing a gap that may be formed between a proximal portion of a femur and a backside of the stem. The stem has an upper end portion 11 to face a proximal side and a backside 15 to face a greater trochanter 33 and is adapted for insertion into, and fixation to, a medullary space of a femur, and the stem has a through bore 17 opened both to said upper end portion and the vicinity of proximal end of said backside.

A male prosthetic device configured to be worn on a flaccid, partially-erect or erect penis which transmits tactile sensations through a stimulation material to the surface of the penis. The device includes a prosthesis with an outer surface and in inner chamber, a microprocessor, one or more sensors and one or more stimulation materials. The outer surface is configured to appear as a penis or other elongate body with hard or soft materials, with optional stimulation materials and sensors. The inner cavity is lined with stimulation material configured to contact the surface of the penis. Sensors for detecting sensation or direction can be disposed within, on, or separate from the device transmit signals electrically or wirelessly to the microprocessor, which is programmed to generate stimulation sensations in response to signals from the sensors, stimulation materials, or controllers that are transmitted to the stimulation material.

An inflatable penile prosthesis cylinder of the present invention includes an inflatable chamber and a constraining sleeve of fabric. The inflatable chamber is configured to expand in response to an increase in pressure within the chamber. The sleeve of fabric constrains the expansion of the chamber, however, the sleeve of fabric includes a corrugation that facilitates some expansion of the sleeve.

Surgical implants and procedures for restoring erectile function are described. One method includes the steps of providing an inflatable prosthesis system with a pump, a cylinder, a septum, and a reservoir, the system having sufficient fluid to inflate the cylinder and reservoir, implanting the system in an inflated condition and leaving the system in this condition in the post-operative period, then inserting a needle through the septum and withdrawing some fluid from the system. The systems of the invention may include the insertion of a needle through the septum for the injection of an antimicrobial or antibiotic.