Abstract: Embodiments include implantable valves with attached polymeric components. In an embodiment, an implantable valve is included having a frame comprising a plurality of frame struts. The frame defines a central lumen and at least one of the frame struts defines a connection aperture. The implantable valve can include at least one valve leaflet including a coaptation edge and two connection portions, with one connection portion disposed on either end of the coaptation edge. The connection portion can be disposed within the connection aperture thereby coupling the valve leaflet to the frame. Other embodiments are also included herein.

Abstract: According to an aspect, an inflatable penile prosthesis having an inflatable member; a reservoir configured to hold fluid; and a pump assembly configured to facilitate a transfer of the fluid from the reservoir to the inflatable member when the prosthesis is in an inflation mode, and facilitate a transfer of the fluid from the inflatable member to the reservoir when the prosthesis is in a deflation mode, the pump assembly including a valve housing and a reinforced pump bulb member.

Abstract: According to an aspect, a penile implant includes a first member having a coupling portion and a locking portion and a second member having a coupling portion and a locking portion. The coupling portion of the first member is configured to engage the coupling portion of the second member to movably couple the first member to the second member such that the first member is configured to be placed in a first position with respect to the second member and a second position with respect to the second member. The locking portion of the first member is configured to engage the locking portion of the second member help retain the first member in its second position with respect to the second member.

Abstract: The invention pertains to implants that facilitate tissue expansion while not substantially inhibiting normal anatomical movement. The implants may be made of different materials or made in different configurations such that such that a measured property at a first location on said implant is different than said same measured property at a second location on said implant. In one particular embodiment the implants may be a cosmetic penile implant.

Abstract: A method of implanting a shoulder prosthesis in a scapula of a patient includes the step of placing a guide over a primary glenoid component previously implanted within the scapula of the patient. The method further includes the steps of removing the primary glenoid component from the scapula and preparing the scapula for implantation of a secondary glenoid component, wherein the removing and preparing steps occur simultaneously.

Abstract: An interbody spacer for the spine is provided. The interbody spacer includes a cage and at least one bone screw configured to anchor the cage between two vertebrae of the spine. The cage includes a lock rotationally movable with respect to the cage between a locked configuration and an unlocked configuration. When in an unlocked configuration, bone screws may be inserted and removed from the cage. When in a locked configuration, the insertion and removal pathway of the bone screw is blocked by the lock, thereby, providing backout protection for the bone screws. The lock is coupled to the cage by a pronged retainer and includes a camming surface to provide for incremental rotation of the lock. The lock includes a space-saving shape providing for maximum bone screw angulation on a laterally smaller anterior platform.

Abstract: An expandable fusion device is capable of being installed inside an intervertebral disc space to maintain normal disc spacing and restore spinal stability, thereby facilitating an intervertebral fusion. The fusion device may include a body portion, a first endplate, and a second endplate, the first and second endplates capable of being moved in a direction away from the body portion into an expanded configuration or capable of being moved towards the body portion into an unexpanded configuration. The fusion device is capable of being deployed and installed in both configurations.

Abstract: A joint implant system adapted for use in joint surgeries. Among other things, the joint implant has an anterior cutting edge and a rotatable cutter supported by a rotatable shaft.

Abstract: An expandable cage for placement between adjacent vertebrae having two or more upper and lower end plates having compound-angled slots, ramps or rails, and a drive means having corresponding compound-angled slots, ramps or rails configured to slidingly engage the compound-angled slots, ramps or rails of the two or more upper and lower end plates, wherein movement of the drive means in a first direction moves the two or more upper and lower end plates away from each other both vertically and horizontally to expand both a height and a width of the expandable cage from a collapsed state to an expanded state.

Abstract: A computer-assisted surgery system comprises a calibrating instrument adapted to be applied to a pelvis in a known manner, and a surgical instrument. A computer-assisted processor unit operating a surgical assistance procedure and comprises at least one portable inertial sensor unit configured to be connected to the at least one calibrating instrument and the at least one surgical instrument, the portable inertial sensor unit outputting readings representative of its orientation. A geometrical relation data module provides a geometrical relation data between the orientation of the portable inertial sensor unit, of the calibrating instrument and of the surgical instrument.

Abstract: A measurement device is provided for measuring a resected femoral head. The device comprises a base (102) with a support rod (104) extending transversely from the base and extending in a direction corresponding to a height of a resected femoral head. A femoral head support (108) is attached to a base proximate an end of the support rod (104) for supporting a severed end of a femoral head at a selected incline between about 30° and 60° relative to the base such that a height of the resected femoral head extends in the general direction of the support rod. A transverse height indicating arm (120) is adjustable up the height of the support rod (104) so as to measure the height of a resected femoral head (106) positioned on the femoral head support in use. The transverse height indicating arm (120) may carry adjustable offset indicating arm (122).

Abstract: An orthopedic surgical device and method of using thereof is provided. The orthopedic surgical device includes a sensor portion including a conformable pad sized for positioning within a knee joint of a patient. The pad includes a femoral side and a tibial side and a sensor array disposed between the femoral side and the tibial side configured to generate a signal indicative of the force within the knee joint. The tibial side includes an adhesive coating. The orthopedic surgical device also includes a display portion including a display and a controller. The controller is configured to receive the signal from the sensor array and to control the display to provide a visual indication of the force within the knee joint.

Abstract: A limb support device includes a variable stiffness mechanism. The limb support device can be an orthotic or prosthetic device. The variable stiffness mechanism can include, for example, a rate-sensitive or speed-dependent material or a damping mechanism. The variable stiffness mechanism causes the limb support device to exhibit different properties when the user of the limb support device is walking at high or fast walking speeds compared to low or slow walking speeds. The limb support device can exhibit high damping and energy absorption, and therefore stability, at slow speeds, and high energy return at faster speeds.

Abstract: A delivery apparatus can include a handle portion and at least one rotatable drive shaft. The handle portion has an actuation mechanism. The actuation mechanism includes a motor and one or more actuators. The rotatable drive shaft has a proximal end portion and a distal end portion. The proximal end portion is coupled to the motor, and the distal end portion is configured to be releasably coupled to a prosthetic heart valve. The actuation mechanism is configured to control and monitor expansion of the prosthetic heart valve. The handle is configured for actuating the actuation mechanism, tracking a response of native tissue when the prosthetic heart valve is in contact with the native tissue, and stopping expansion of the prosthetic heart valve once a rate of change of expansion of the prosthetic heart valve declines below a threshold.

Abstract: A vascular intervention device delivery system includes a thumbwheel rotatably mounted in a handle. A termination assembly is mechanically connected to the handle. A catheter extends through the termination assembly and has a proximal end attached to the handle, and a distal carrier segment for mounting a vascular intervention device. A retractable sheath is movable from a first position covering the distal carrier segment to a second position retracted proximally to uncover the distal carrier segment. A pull extends between the thumbwheel and the retractable sheath, and through the termination assembly. A stability sheath that receives the pull and the inner catheter has a proximal end that terminates in the termination assembly.

Abstract: Apparatus and methods are provided for flaring a stent deployed within a branch vessel including an ostium communicating with a main vessel, a first end of the stent extending at least partially from the branch. A catheter is provided that includes a first balloon carried on its distal end, and a second balloon that includes a distal section overlying at least a portion of the first balloon and a proximal section. The catheter distal end is introduced into the main vessel and positioned through the ostium and stent into the branch until the first balloon is disposed within the stent. The first balloon is expanded to anchor the stent, and the second balloon is expanded to flare the first end of the stent. Optionally, the first balloon is expanded further, e.g., to expand the stent within the branch body lumen and/or dilate the lesion.

Abstract: Intravascular delivery system for deployment of a therapeutic device, such as a stent, in a controlled and robust manner is supported by a lockable balloon catheter equipped with a locking mechanism configured to lock in vivo to a delivery component, such as a guidewire. The lockable balloon catheter can be controllably transitioned between a locked and an unlocked modes of operation by inflation/deflation of the balloon of the lockable balloon catheter. Being in the locked mode of operation, the lockable balloon catheter facilitates delivery of the therapeutic element along the delivery component to a target site while enhancing the stability of the delivery component, especially near the target site.

Abstract: A method of performing bariatric surgery includes inserting a gastrectomy device into a stomach of a patient, positioning the gastrectomy device in a selected location in the stomach, transecting a portion of the stomach thereby reducing a size of the stomach, and applying a reinforcement scaffold to an outer surface of the stomach. The reinforcement scaffold is configured to maintain the reduced size of the stomach.

Abstract: A dynamic foot plate assembly structured for therapeutic use adjacent the ankle area of the body comprising a base element, at least one side element extending along the ankle area, and at least one joint movably and adjustably connecting the base element to the side element for variable displacement of the base element and side element into different operative orientations. The dynamic foot plate assembly may also comprise a plurality of strut members disposed in an interconnecting relationship between either a support member and a side element, or the support member and the base element. The strut members, if present, facilitate the variable relative displacement of the base element, side element and support member into different operative orientations.

Abstract: A removable and replaceable hip orthotic that includes a back panel formed from a rigid material that supports a patient's lumbar area; a front panel formed from the rigid material that supports the patient's abdomen area and is hinged to the back panel to allow application and removal of the orthotic to the patient; a leg support that extends from the back support that includes a space that allows a patient's leg to pass through into the leg support; and straps to secure the back panel to the front panel and the leg into the leg support. The back panel includes a pair of windows with a trochanter pad movably disposed within the windows. An adjustment mechanism selectively moves the trochanter pads relative to the greater trochanter regions of the hips of the patient to apply pressure to the hip joint to prevent dislocation of the femoral head.

Abstract: A spinal orthosis includes posterior panels arranged with a flat spinal curvature to create a reverse three-point pressure system to the spine. The reverse three-point pressure system relieves pressure on the posterior side of the vertebrae beneficial for certain indications. Various arrangements allow for securing the posterior panel to the spinal orthosis. The spinal orthosis includes a belt member length adjustment system including belt members having end portions reducible in length and a belt panel adapted to secure to the end portion of the belt member reduced in length to form at least in part a belt circumference of the spinal orthosis.

Abstract: A nasal support device includes a device body. The device body defines a perimeter shape of the nasal support device and also can include a nasal support structure. The nasal support device also includes adhesive carried with the device body. The nasal support device further includes a peelable backing that covers the adhesive and includes at least one peelable backing piece that is divided into a first section and a second section by a pre-defined fold location. The pre-defined fold location is configured such that the first and second sections of the peelable backing piece remain coupled together at the pre-defined fold location after folding at the pre-defined fold location.

Abstract: A head positioning aid includes at least one head positioning assistor and at least one securing member. Some head positioning aids include positioning members secured to a headwear member. The positioning members maintain an infant's head in midline. An optional cheek flap protects the skin on the face. An optional support member supports the neck and an open airway. Size adjustment members may also be used to secure and orient tubing for a nasal cannula.

Abstract: The present invention comprises a kit of a restraint ring, a base and a quick release, tamper resistant fastener. The base is adapted to attach to a fixture. The fixture may be a bed, chair, floor or wall. The base may be attached using tamper resistant fasteners. The base may be permanently attached or may be removably attached. The base is adapted to releasably receive the quick release fastener thereby attaching the restraint ring to the base.

Abstract: A multilayer film includes an outer foam layer and a gas barrier layer. The multilayer film may also include at least one tie layer and at least one inner layer, and can be configured to have various film layer constructions. For example, the multilayer film can be configured as a five-layer, six-layer, or seven-layer films. The multilayer film can provide unique texture, softness, quietness, gas barrier properties, light weight and low cost per volume. Further, one or more layers of the multilayer film can contain a vinyl-bond rich triblock copolymer to provide sound absorbing properties.

Abstract: An asymmetric multilayer film for an ostomy pouch includes a barrier layer including a first side and a second side. At least one layer is arranged on the first side of the barrier layer, and at least one layer arranged on the second side of the barrier layer, in which the combined thickness of the at least one layer arranged on the first side of the barrier layer is at least two times greater than the combined thickness of the at least one layer arranged on the second side of the barrier layer. The asymmetric multilayer film has a thickness of about 25 ?m to about 50 ?m.

Abstract: An device including a proximal portion adapted for placement intermediately within a hollow body cavity to capture and divert contents; the proximal portion being expandable from an initial state with an initial diameter, into an expanded state with a diameter greater than the initial diameter for engaging the proximal portion with an inner wall of the hollow body cavity; and a distal portion, connected to the proximal portion, adapted to extend through the abdominal wall or into the intestine to conduct the hollow body cavity contents out of the proximal portion.

Abstract: The present subject matter relates to medical devices for ostomy applications, specifically a floating ring design for securing robust attachment between the flange surrounding a stoma on a patient's body and an ostomy bag. Existing ostomy appliance designs present significant drawbacks related to routine, high replacement cost and poor performance, the latter resulting in anxiety, grief over fear of stool leakage due to rapid, sudden and/or unexpected detachment or mechanical compromise of ostomy appliance components. This further includes discomfort due to the mechanical stresses placed on the subject's body.

Abstract: The purpose of the present invention is to provide a heat generator that contains a volatile component and in which the volatile component is stably maintained during storage, the volatile component is prevented from adhering to a heat-generating section, and it is possible to achieve an excellent warming effect during use. This heat generator comprises a heat-generating section (1), an accommodation body (2) for accommodating the heat-generating section (1), an adhesive layer (3) provided to an attachment surface side of the accommodation body (2), and a release sheet (4) provided to the attachment surface side of the adhesive layer (3). As a result of including a volatile component in the adhesive layer (3) and respectively providing gas barrier layers (211), (41) to a first packaging material (21) constituting the attachment surface side of the accommodation body (2) and to the release sheet (4), it is possible to stably maintain the volatile component within the adhesive layer (3) during storage.

Abstract: An in-ear stimulator for administering thermal stimulation to the ear canal of a subject includes (a) an earpiece configured to be insertable into the ear canal of said subject, the earpiece having an outer surface and an internal cavity formed therein, the internal cavity having an inner surface; and (b) at least one thermoelectric device thermally coupled to the earpiece internal cavity inner surface.

Abstract: Devices can be implanted in an eye to treat a dry eye condition. The devices include a body defining a lumen and having first and second ends and external and lumenal surfaces. The body has a length sufficient to provide fluid communication between the anterior chamber and tear film of the eye through the lumen when the device is implanted in the sclera. In some embodiments, the device is filterless. In some embodiments, a filter is included. The dry eye treatment devices provided herein prevent bacterial ingress, provide outflow resistance to retain a normal intraocular pressure, and provide moisture (e.g., aqueous humor) to an otherwise dry eye. Methods of treating a dry eye condition wherein the device is implanted in the sclera of an afflicted eye are also described.

Abstract: A surgical cassette for use with a phacoemulsification system having a front plate, a back plate, and a gasket therebetween. The front plate having molded fluid channels that mate with the gasket. The gasket having multiple valves and a sensor or diaphragm accessible through the back plate.

Abstract: A water jet instrument may be used for manually performing surgery. The water jet instrument may be manually controlled or controlled by a system with a robotic control. The water jet apparatus defines a jet cutting area that is based at least in part on a flow rate meter and a feedback loop.

Abstract: Drainage of body fluid from a first area of the body to a target area of the body can be accomplished by interconnecting an artificial non-blood fluid conduit with the venous and/or lymphatic system of the body. For example, an artificial non-blood fluid conduit can be inserted into the eye to fluidly interconnect the anterior chamber with a venous structure, such as an anterior ciliary vein, or lymphatic in a target location of the eye. The outflow end of the conduit can be positioned adjacent to and/or cannulated within the venous structure or lymphatic. Further, the conduit can optionally have an angiogenic material for stimulating growth of new blood vessels in the target location to fluidly interconnect the venous structure or lymphatic with the anterior chamber using the non-blood fluid conduit.

Abstract: The present disclosure provides a system for femtosecond ophthalmic surgery in which the position of a suction cone in the z direction is measured via the measuring device to generate data that is processed and used to create a pictorial representation, a histogram, or other graph based on the data. The pictorial representation may include at least one threshold marker. The disclosure further provides a method of performing docking in femtosecond laser ophthalmic surgery including measuring the position of a suction cone with a measuring device, and transmitting data regarding the position to a processor which processes the data and uses it to create a pictorial representation, histogram, or other graph that is presented on a display.

Abstract: A medical dressing is provided. The dressing has a central portion and a border portion, and comprises a backing layer, an adhesive body contact layer and a pad arranged in the central portion between the backing layer and the adhesive body contact layer. The pad is symmetric about a longitudinal center line and the dressing comprises a lobed portion on each side of the center line. The medical dressing comprises a gripping tab which is coplanar with the border portion and which projects outwardly from the border portion. The medical dressing may be used for pressure ulcer prevention, such as at the sacrum region of a human body.

Abstract: A therapeutic compression garment, including: a body portion; and a spine portion, wherein the bands extending from either the body portion and/or spine portion attach the body and spine portions together when the body and spine portions are wrapped around a body limb, and wherein the spine portion is releasably attached onto the body portion such that the spine portion is positionable at different locations on the body portion.

Abstract: A nose compression device for treating a nosebleed of a person. The device includes a wire frame having a straight middle section and two end sections angled with respect to the middle section. The device also has a body attached to the wire frame, and two nasal sponges attached to the body for insertion into the person's nasal passages. The end sections are wider than the user's nose, and the device is slid upward on the user's face so that the nasal sponges enter the user's nasal passages. The end sections are then bent inward to a pinch position where they pinch the upper lateral side surfaces of the user's nose. The nasal sponges can be pre-treated with medication to further stop the nosebleed. Ice pack may also be provided that extends over the compression device. The combination of compression, medication, and cooling facilitate treatment of the nosebleed.

Abstract: Methods for deforming a multilayer web are disclosed. Steps of the method include: supplying a first layer of a precursor web; supplying a second layer of the precursor web onto at least the first area of the first layer; forming a plurality of first features and a plurality of second features in the precursor web. The plurality of first features are apertures formed in a first area of the precursor web, and the plurality of second features are formed in a second area of the precursor web in a positive and/or negative Z-direction. The plurality of first features and the plurality of second features are formed simultaneously.

Abstract: A stretchable/contractible sheet having an up-down direction and a left-right direction intersecting each other is provided. The stretchable and contractible sheet includes: a first welded-portion row including a plurality of welded portions arranged side-by-side in the up-down direction; and a second welded-portion row including the plurality of welded portions located adjacent to the first welded-portion row on a one side in the left-right direction. The first welded-portion row includes: a first convex portion protruding toward the one side; and a second convex portion. The second welded-portion row includes a third convex portion protruding toward another side opposite to the one side in the left-right direction.

Abstract: An absorbent article for wearing about the lower torso of a wearer includes a first waist region having a first waist edge, a second waist region having a second waist edge, and a crotch region disposed between the first and second waist regions. The article further includes a first longitudinal edge, a second longitudinal edge, and a chassis having a topsheet, a backsheet, and an absorbent core disposed between the topsheet and backsheet. A waist gasketing element is joined to the chassis and disposed in one of the first waist region or the second waist region. The waist gasketing element has a top layer and a bottom layer, an inboard lateral edge and an outboard lateral edge, and first area, A1. The top layer is bonded to the bottom layer in a closure bond region by a closure bonding technique. The closure bond region has an aggregate closure bond area, BA, which is at least about 10% of the first area, A1.

Abstract: The present invention provides a sanitary pad including an upper sheet made of pure organic cotton through which a liquid is permeable, a first absorbing sheet disposed below the upper sheet and made of pure organic cotton configured to absorb the liquid, a second absorbing sheet disposed below the first absorbing sheet and made of natural compressed pulp configured to absorb the liquid, and a waterproof sheet disposed below the second absorbing sheet and having air permeability.

Abstract: A first aid kit including a bottom in which to carry a first number of first aid products, a cover pivotally connected to the bottom and rotatable between closed and open positions lying over and away from the bottom, and an auxiliary tray having rotatable storage shelves at which a second number of first aid products are carried. The auxiliary tray is pivotally connected to the bottom of the first aid kit and rotatable between a folded position lying within the bottom of the kit and an unfolded position lying slightly above and to one side of the bottom to create a multi-level product storage configuration. A mounting bracket carried by the first aid kit is detached therefrom and connected to a wall. The first aid kit is reattached to the bracket, whereby the kit is suspended from the wall by the bracket.

Abstract: A spinal immobilization device including a base member and a spinal support member configured to overlay the base member. The base member includes an elongate board having a curvate top surface, and a channel defined within the top surface. The spinal support member may include a bladder, a fluid housed within the bladder, a plurality of fluid absorbing members within the bladder, and a breakable barrier separating the fluid and the plurality of fluid absorbing members from mixing. The channel defines an impression within the top surface that matches a shape of a portion of the bladder.

Abstract: An autonomous stretcher intended for patients with reduced mobility, particularly quadriplegic and paraplegic, is adjustable in height and transformable between a horizontal position in the manner of a bed for housing the patient lying down and a staggered position in the manner of a chair. It incorporates transport litters destined for supporting the patient, endowed with movement in a transverse direction to the supports in both directions of movement: towards the exterior of the stretcher to remove the patient from the stretcher, for example towards a bed or a wheelchair and towards the interior of the stretcher to accommodate the patient therein. It makes it possible to modify its longitudinal or transverse orientation with respect to the frame and enables the patient to satisfy his or her physiological evacuation needs through the stretcher itself in a sitting position.

Abstract: A wheelchair lift includes a platform assembly to receive a wheelchair, and a lifting assembly to move the platform assembly, a supporting plate to support the lifting assembly, and a supporting arm to support the platform assembly. The lifting assembly includes a pair of a first lifting arm and a second lifting arm. The first lifting arm has a bent shape along the longitudinal direction of the first lifting arm, and the second lifting arm has a bent shape along the longitudinal direction of the second lifting arm.

Abstract: A connection assembly for coupling an auxiliary drive system to a wheelchair for disabled people, of the type comprising a fixing structure adapted to be fixed to the framework of the wheelchair and a longitudinal member operatively connected to the fixing structure so that the longitudinal development axis of the longitudinal member is substantially parallel to the advancement direction of the wheelchair. The connection assembly comprises connection means associated with the free end of the longitudinal member and with the auxiliary drive system, such connection means are configured to allow rapid coupling and decoupling of the auxiliary drive system to/from the wheelchair.

Abstract: A collapsible mobility aid with two frame elements, on each of which at least one wheel is secured or can be secured, and with a folding mechanism by which the frame elements are connected to each other, and a distance between the frame elements in a first position of the folding mechanism can be adapted to a transport distance and in a second position of the folding mechanism can be adapted to a use distance, wherein the folding mechanism has a central element with a slide arranged moveably with respect thereto, at least two connection arms which are each articulated on a frame element and on the central element, and at least two levers which are each articulated on a connection arm and on the slide, wherein the swivel axes, about which the levers are arranged on the connection arms and the slide such that they can be swiveled, are on one plane when the folding mechanism is in the second position.

Abstract: A patient support apparatus comprises a base and a support structure coupled to the base and being configured to support a patient. The apparatus also comprises a panel having a surface and being physically adapted to vibrate at one or more frequencies, a controller configured to generate an electrical signal, and a vibrational exciter. The vibrational exciter comprises a surface coupled to the surface of the panel and being configured to receive the electrical signal from the controller and to convert the electrical signal into vibrational energy. The surface of the vibrational exciter is configured to transfer the vibrational energy to the surface of the panel to vibrate the panel at the one or more frequencies.

Abstract: The hospital bed with pivoting side rail includes a bed frame having a headboard, a footboard and a platform mounted thereon. The side rail has an upper end, a lower end, and first and second longitudinally opposed sides. The lower end of the side rail is pivotally attached to the bed frame, and the upper end of the side rail is releasably attached to the headboard and the footboard. In order to safely and easily deploy and collapse the side rail, first and second adjustable struts are provided, the struts having opposed first and second ends, such that the first ends of the first and second adjustable struts are pivotally attached to the first and second sides of the side rail, and the second ends of the first and second adjustable struts are pivotally secured to the headboard and footboard, respectively.