Abstract: Disclosed herein is a sleeve for reducing involuntary leakage of a flowable material from a urethral meatus of a penis. The sleeve comprises a body that is configured to temporarily receivably retain a glans penis. When the glans penis is temporarily receivably retained by the body, the body applies an inwardly-directed pressure to the glans penis to close a urethral meatus of the glans penis.

Abstract: A method for repairing a defective heart valve includes directing a delivery catheter to form a first curve around the heart valve at a first side of the heart valve leaflets and forming a second curve of the delivery catheter around the heart valve on a second side of the heart valve leaflets. The first and second curves are connected through a commissure of the heart valve and an annuloplasty implant is ejected from the delivery catheter while the delivery catheter is retracted such that the annuloplasty implant is arranged along the first and second curve.

Abstract: A face shield includes a front surface opposite of a back surface, a shield portion, and a band portion extending from a top side of the shield portion. A plurality of spacing projections extend outward from the back surface of the face shield that are configured to be positioned against a forehead of a wearer.

Abstract: An orthotic joint device has an attachment member rotatably attached to the joint device for rotation in a first direction, a resistive element such as a spring, and a first lever for transmitting a first direction resistance force from the resistive element to the attachment member. The resistive element may also resist rotation in the second direction opposed to the first via a second lever. The orthotic joint device may be used in an orthosis and in a method of supporting an ankle of a human.

Abstract: A knee brace includes a flexible sleeve made of a flexible fabric; a memory device configured to store a reference configuration of the flexible sleeve; a first sensor configured to detect a configuration of the flexible sleeve; and a sleeve tightening mechanism configured to adjust a tightness of the flexible sleeve. A controller is configured to receive an output signal representing, or indicative of, the detected configuration from the first sensor, compare the detected configuration with the reference configuration, and control the sleeve tightening mechanism based on a result of a comparison of the detected configuration of the flexible sleeve and the reference configuration of the flexible sleeve.

Abstract: A taping method that follows a specific set of rules based on anatomical and physiological patterns in humans. This taping method causes a change in skeletal muscle tone in the human body when tape is directly applied to the skin of the human body over the targeted muscles. This taping method will inhibit the muscle tone in the affected motor units that are underneath the tape applied in a specific inhibition method. This taping method will elicit the muscle tone in the affected motor units that are surrounded by the tape applied in a specific elicitation method. There are three different types of elicitation method patterns based on muscle size or groups of muscles, secondarily to the length tension relationship required for a muscle contraction. There is only one type of inhibition method.

Abstract: A pediatric position holder for holding a child in a position is provided. The pediatric position holder includes a central panel extending longitudinally from a cranial portion to a caudal portion, arm flaps extending outwardly from opposing sides of the central panel, and leg flaps extending outwardly from opposing sides of the central panel. The arm flaps each include a proximal arm segment and a distal arm segment extending from the proximal arm segment. The leg flaps each include a proximal leg segment that defines one cutout and a distal leg segment extending from the proximal leg segment. The pediatric restraint is configurable between an initial, open configuration and a second, closed configuration in which the distal arm segments of the arm flaps overlap one another, and the distal leg segment of each of the leg flaps is positioned within the cutout of the respective leg flap.

Abstract: A splint and a method for operating a splint are disclosed. The splint includes a plurality of plates, at least one rope, and at least one fastening drive device. The plurality of plates include a first plate. The rope is in movable connection with the plurality of plates. The fastening drive device is on the first plate, and is connected to the rope and configured to drive the rope under control, so as to allow the rope to be tightened or loosened under drive of the fastening drive device to drive the plurality of plates to move relatively close to each other or relatively away from each other.

Abstract: An orthopedic implant with an inferior portion having a tibia contact surface configured to extend over a tibia; a superior portion opposite to the inferior portion having a tendon contact surface configured to change a position of a patellar tendon by lifting or tilting the patellar tendon when the curved surface of the first portion is engaged with the tibia; and a fixation mechanism adapted to attach the orthopedic implant to the tibia, the orthopedic implant being further configured to change shape from a first configuration to a second configuration in response to a load applied between the tendon contact surface and the tibia contact surface. The invention also addresses corresponding methods.

Abstract: The present disclosure relates generally to the field of medical devices. In particular, the present disclosure relates to delivering a variable length stent within a patient. In one example, a stent may include a body comprising coils about a longitudinal axis of the stent and along the length of the stent between a proximal end and a distal end in a substantially helical pattern. The coils may define a lumen along the longitudinal axis through the center of the body. A distal tube may have a wall extending from the distal end of the body. A first aperture may extend through the wall of the distal tube into the lumen. A distal retention member may extend from the distal tube. A distal suture may have a mid-portion. The mid-portion may extend through the first aperture.

Abstract: Ankle foot orthoses and methods of manufacturing an ankle foot orthosis. In one embodiment, an ankle foot orthosis is disclosed that includes a foot plate constructed to have both a trimmable portion and a non-trimmable portion. The ankle foot orthosis includes a spiral strut coupled with either the hindfoot region of the foot plate laterally of a mid-line for the foot plate or the midfoot region of the foot plate laterally of the mid-line. The spiral strut includes a transition portion that spirals by approximately sixty-five degrees (65°) over less than one-hundred sixty millimeters (160 mm) in height from the bottom surface of the foot plate. The spiral strut also includes an adjustable portion that enables a cuff coupled thereto to be height adjustable. Methods of manufacturing the aforementioned ankle foot orthoses are also disclosed.

Abstract: A hamstring support system comprising a waist strap, a heel cup and an elongated biasing element assembly elastically extending between the waist strap the heel cup. The waist strap is secured to a waistline of a patient having an injured or recovering hamstring injury. The heel cup is secured to a heel of an injured leg of the patient. A length of the biasing element assembly is adjusted to a neutral or slight biasing force when the injured leg is bent, thus providing a supporting force when the injured leg is extended. A pliant material can be placed between the heel cup and the heel. A shoe is preferably worn over the heel cup.

Abstract: A vascular graft deployment tool may include a grip, an elongated mandrel positioned distal of the grip, a vascular graft, at least part of which is disposed coaxially about the mandrel, a sheath configured to be withdrawn proximally that constrains the vascular graft against the mandrel in an insertion diameter and an actuator that is moveable relative to the grip and engages the sheath assembly. A first operation of the actuator causing withdrawal of the sheath to free at least a distal portion of the vascular graft and a repeated operation of the actuator causing further withdrawal of the sheath to free a proximal portion of the vascular graft.

Abstract: A textile graft includes a tubular wall disposed between a first open end and an opposed second open end and having an inner surface and an opposed outer surface. The tubular wall includes a textile construction of one or more filaments or yarns, the textile construction by itself being permeable to liquid. A portion of the inner surface of the tubular wall includes a coating of a substantially water-soluble material thereon. The outer surface includes a coating of a substantially water-insoluble elastomeric sealant disposed thereon. The tubular wall having the coating of the substantially water-insoluble elastomeric sealant is, after curing thereof, substantially impermeable to liquid.

Abstract: Disclosed are methods and devices for regulating fluid flow to and from a region of a patient's lung, such as to achieve a desired fluid flow dynamic to a lung region during respiration and/or to induce collapse in one or more lung regions. Pursuant to an exemplary procedure, an identified region of the lung is targeted for treatment. The targeted lung region is then bronchially isolated to regulate airflow into and/or out of the targeted lung region through one or more bronchial passageways that feed air to the targeted lung region. An exemplary flow control device is configured to block fluid flow in the inspiratory direction and the expiratory direction at normal breathing pressures and allow fluid flow in the expiratory direction at higher than normal breathing pressures.

Abstract: Methods and apparatus for an orthopedic device. In one embodiment, the orthopedic device includes a first panel defining opposed first and second sides; a second panel having a first end secured to the first side of the first panel along a seam, and a second end securable to the second side of the first panel at a location site; and a first strap having a first end secured to the first side of the first panel along the seam and laying under the second panel, and a second end securable to the second side of the first panel at the location site. The orthopedic device may include a dynamic force strap that includes three ends, that collectively helically extend between upper and lower portions of the orthopedic device and connect to the first panel.

Abstract: An orthopedic implant apparatus, said apparatus comprising: a body, said body having a generally cylindrical shape and comprising a first material, a flat bottom surface, a concave upper surface disposed opposite said bottom surface, and a longitudinal axis disposed through the center of said body; a cylindrical bore, said bore disposed along said longitudinal axis through said top surface of said body; cylindrical plug, said plug comprising a second material and disposed within said bore of said body; and at least one stem, said at least one stem connected to said bottom surface of said body.

Abstract: An apparatus for use in a surgical procedure for delivering a prosthetic implant comprises a flexible sleeve configured with a first end and a second end, the flexible sleeve being tapered such that a width of a region at the second end is relatively smaller than a width of a region at the first end, and an interior surface of the flexible sleeve that form an interior cavity, the interior cavity being sized to receive the prosthetic implant; one or more surface active coatings are applied to the interior cavity. The flexible sleeve is manipulatable such that when the prosthetic implant is positioned within the interior cavity, a manually applicable directional pressure in the direction of the second end causes the prosthetic implant to extrude from the second end.

Abstract: A method of making an implantable prosthesis includes applying a gelling enhancer layer over an inner surface of a wall of a silicone shell having anterior and posterior walls surrounding an interior volume. The method includes filling the interior volume of the shell with a silicone gel and curing the silicone gel. The cured silicone gel that is located within a zone that is in the vicinity of the gelling enhancer layer has a higher level of cohesiveness than the cured silicone gel that is located outside the zone. The zone of the silicone gel having the higher level of cohesiveness has a thickness of 2-10 mm. The silicone gel located outside the zone has a first concentration level of a gelling enhancer and the silicone gel located within the zone has a second concentration level of the gelling enhancer that is 5%-300% greater than the first concentration level.

Abstract: An endovascular medical assembly and method for restoring chordal support to a leaflet of a heart valve by implanting artificial chordae tendinea in the heart. A chord is inserted into the heart endovascularly with a leaflet grasper which pierces the leaflet and implants the chord through the leaflet. An anchor assembly is implanted into an intracardiac wall and has anchor lines extending therefrom. The chord and an anchor line are assembled by a line gathering member and the tension of the chord is adjusted and secured. The chord is, thus, secured to the anchor assembly to support the leaflet.