Abstract: The present invention relates to a musical instrument for producing a harmonious scale of musical notes. The instrument includes nine separate sound actuators each of which is configured to cause the musical instrument to generate a different frequency selected from the group of frequencies comprising 174 Hz, 285 Hz, 396 Hz, 417 Hz, 528 Hz, 639 Hz, 741 Hz, 852 Hz and 963 Hz, the musical instrument being configured such that physically manipulating the sound actuators causes the musical instrument to generate the frequency corresponding to the sound actuator manipulated. The invention is also directed at a system for—writing music to be played with a musical instrument incorporating the harmonious scale of musical notes as described above.

Abstract: Rear tip extenders having a tether attached to a collar for penile implants that can be mounted onto a respective cylinder forward of a fluid line (that communicates with a scrotal pump) to prevent full separation or detachment from the cylinder during a revision procedure can be fabricated by molding. The fabrication methods include: providing a mold with a mold cavity configured to define three attached members of defined shapes, including a rear tip extender, a collar and a tether attaching the rear tip extender and collar; and flowably introducing moldable material into the mold cavity to form the collar, rear tip extender and attached tether as a molded assembly.

Abstract: Method and system for treating a patient using an inflatable device. A removal device may be used to remove the inflatable device from the body. The removal device can have at least one manually-actuatable member and at least two opposing jaws at a distal end. At least one of the at least two jaws can be movable by actuation of the at least one manually-actuatable member. At least one of the at least two jaws can have a puncturing member.

Abstract: An implant is disclosed. The implant includes a reinforcement component attached to a sheet component. The sheet component is formed as a porous and fibrous material. The implant is adapted to be implanted on an area of a penis having Peyronie's plaques excised. The implant will elongate during erection of the penis and contract when the penis returns to a flaccid state. The reinforcement component includes a longitudinal rod and a transverse connector, with the longitudinal rod providing column strength to the implant and the sheet component providing support for penile tissue.

Abstract: A pump adapted for use with an implantable penile prosthetic includes an inlet flow path formed in a pump body having a first portion communicating between a reservoir and an inlet valve and a second portion communicating between the inlet valve and the pump bulb. The inlet valve includes a spherical part having a groove formed on an exterior surface of the spherical part.

Abstract: An assistance system for visually handicapped persons with visual impairment in a part of their visual field includes body-worn sensors to inform them actively about objects or movements in the visually impaired sides.

Abstract: A method and morphologically adaptable apparatus for altering the charge distribution upon living membranes is provided. The method and apparatus further provides a static magnetic device for production of a magnetic field for treatment of various disorders that can be focused at the site of pain or edema to deliver a gradient in the magnetic field to prevent or reduce charge flow. Further there is provided a static magnetic device for production of a magnetic field for treatment of disorders wherein the device provides a static magnetic field such that the focused magnetic field gradient is oriented to be perpendicular to the neuron or membrane charge flow providing maximum deflection of the ion or charge flow.

Abstract: A tool adapted for inserting a penile prosthesis into a penis includes a first neck connected to a first end of a handle and a second neck connected to a second end of a handle, and a first guide connected to the first neck and a second guide connected to the second neck. The first guide has a first cylinder cradle and the second guide has a second cylinder cradle.

Abstract: In an embodiment, a medical device is a bodily implant and includes an elongate member. The elongate member has an inner edge that defines an opening. At least a portion of the inner edge being treated.

Abstract: A radiation system includes: a first support; a first structure rotatably coupled to the first support so that the first structure is rotatable about a first axis relative to the first support; a second structure rotatably coupled to the first structure so that the second structure is rotatable about a second axis that forms a non-zero angle relative to the first structure; and a first radiation source connected to the second structure; wherein the first structure and the second structure are parts of a capsule for accommodating at least a portion of a patient.

Abstract: A method of providing a patient with an implanted penile prosthetic adapted to provide improved flow of blood to a glans penis dilating a first portion of tissue in the corpora cavernosum and creating a first space and leaving a segment of vascularized tissue in the corpora cavernosum un-dilated and undisturbed, and engaging a channel formed in an exterior surface of a penile prosthetic with the segment of vascularized tissue.

Abstract: A treatment planning system (106) for generating patient-specific treatment margins. The system (106) includes one or more processors (142). The processors (142) are programmed to receive a radiation treatment plan (RTP) for irradiating a target (122) over the course of one or more treatment fractions. The RTP including one or more treatment margins around the target (122) and a planned dose distribution for the target (122). The processors (142) are further programmed to receive motion data for at least one of the treatment fractions of the RTP from one or more target surrogates (124), calculate a motion-compensated dose distribution for the target (122) using the motion data and the planned dose distribution, compare the motion-compensated dose distribution to the planned dose distribution, and adjust the treatment margins based on dosimetric differences between the motion-compensated dose distribution and the planned dose distribution.

Abstract: An artificial urinary sphincter (AUS) system that includes a reservoir to hold a fluid, a cuff that includes a pre-shaped spiral tube to be wrapped around a urethra, and a control device to be fluidically coupled to the reservoir and the cuff. The control device regulates transfer of the fluid between the reservoir and the cuff. The cuff receives and dispatches the fluid to expand and contract the pre-shaped spiral tube and to coapt the urethra for continence and open the urethra for voiding.

Abstract: A core member for semen collection device includes a flexible body and a built-in piece. The flexible body has a flexible base and an annular sidewall extending from the flexible base to form the cylindrical structure. The built-in piece is disposed in the sidewall of the flexible body. The built-in piece is made of a hard resin material, and the flexible body defines the insertion space having the inlet at the end of the flexible body.

Abstract: Embodiments of the present invention relate generally to the field of tissue repair and regeneration. More specifically embodiments of present disclosure relate to devices or constructs and methods to prepare various devices or constructs useful in directing cellular repair and controlling tissue regeneration to prevent or minimize postsurgical or post traumatic adhesions, excessive scars and/or fibrotic reactions of injured tissues.

Abstract: A cabinet structure for an infusion system includes a platform, on which the system is mounted, and a shell surrounding an interior space, which contains at least a portion of the system. The shell preferably includes an opening that is sized and oriented to allow a lowering of a radioisotope generator, for the system, into the interior space, and a lifting of the generator out from the interior space. The shell may further include another opening, located at a higher elevation than the aforementioned opening, in order to provide access to a waste bottle of the infusion system.

Abstract: The invention relates to a diffusional magnetic patch, which is a medical device for application in the treatment of disc hernia and sports injuries, including a special formulation that acts mechanically with diffusional effect.

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 compact and economical transcranial magnetic stimulation system has a magnetic field generator for generating a magnetic field to be used for providing magnetic stimulation to the head of patient. The generator has a magnetic coil for generating a variable magnetic field and a holder for holding the magnetic coil. The holder has positioning portions for positioning the holder against respective markings on the head of patient. The coil is placed into a suitable posture against certain position by aligning the positioning portions with the markings on the head of patient.

Abstract: Method for transcranial neurostimulation. A target of neurons for transcranial stimulation or modulation is located within an impedance model of the brain, a model of a selected device to be used for producing an electric or magnetic field outside the brain is obtained and used, along with the impedance model, to compute respective virtual target stimulating current vectors representing target stimulating currents that would result from using the device in two distinct trial dispositions of the device, an image of the cortical surface at the target is obtained and used to compute a target normal vector, and a determination is made of which of the two virtual target stimulating current vectors has a greater component projecting at predetermined angles from the target normal vector.