Abstract: A prosthetic valve including an annulus, a pair of leaflets, and a pair of support elements is described. The annulus has a generally saddle-type shape and is connected to the support elements. The pair of leaflets extends from the annulus and are separated from each other by the support elements. In use, the valve is open when the support elements are angled or separated outward, and sealed or closed when the support elements are angled or moved inward.

Abstract: Embodiments described herein address the need for improved catheter devices for delivery, repositioning and/or percutaneous retrieval of the percutaneously implanted heart valves. One embodiment employs a plurality of spring-loaded arms releasably engaged with a stent frame for controlling expansion for valve deployment. Another embodiment employs a plurality of filaments passing through a distal end of a pusher sleeve and apertures in a self-expandable stent frame to control its state of deployment. With additional features, lateral positioning of the stent frame may also be controlled. Yet another embodiment includes plurality of outwardly biased arms held to complimentary stent frame features by overlying sheath segments. Still another embodiment integrates a visualization system in the subject delivery system. Variations on hardware and methods associated with the use of these embodiments are contemplated in addition to those shown and described.

Abstract: The present invention satisfies the long felt need for a more compact and durable valve which may be formed in situ. The present invention provides a self-deployable valve system, a method of delivery, and a method of manufacturing for the self-deployable valve system. The present invention delivers the necessary components for forming a complete valve system in situ. The collapsed subcomponents of the system lack any functional characteristics commonly associated with a valve before being expanded. However, once expanded, the system is transformed into a competent valve for use in a wide variety of applications.

Abstract: Described is a scaffold that is strong enough to resist forces that exist inside a body, while possessing biocompatible surfaces. The scaffold is formed of a layer of mesh (e.g., Stainless Steel or Nitinol) that is tightly enclosed by a multi-layer biological matrix. The biological matrix can include three layers, such a first layer (smooth muscle cells) formed directly on the metal mesh, a second layer (fibroblast/myofibroblast cells) formed on the first layer, and a third layer (endothelial cells) formed on the second layer. The scaffold can be formed to operate as a variety of tissues, such as a heart valve or a vascular graft. For example, the mesh and corresponding biological matrix can be formed as leaflets, such that the scaffold is operable as a tissue heart valve.

Abstract: Described is a scaffold that is strong enough to resist forces that exist inside a body, while possessing biocompatible surfaces. The scaffold is formed of a layer of mesh (e.g., Stainless Steel or Nitinol) that is tightly enclosed by a multi-layer biological matrix. The biological matrix can include three layers, such a first layer (smooth muscle cells) formed directly on the metal mesh, a second layer (fibroblast/myofibroblast cells) formed on the first layer, and a third layer (endothelial cells) formed on the second layer. The scaffold can be formed to operate as a variety of tissues, such as a heart valve or a vascular graft. For example, the mesh and corresponding biological matrix can be formed as leaflets, such that the scaffold is operable as a tissue heart valve.

Abstract: The present invention satisfies the long felt need for a more compact and durable valve which may be formed in situ. The present invention provides a self-deployable valve system, a method of delivery, and a method of manufacturing for the self-deployable valve system. The present invention delivers the necessary components for forming a complete valve system in situ. The collapsed subcomponents of the system lack any functional characteristics commonly associated with a valve before being expanded. However, once expanded, the system is transformed into a competent valve for use in a wide variety of applications.

Abstract: Described is a wireless hemodynamic monitoring system that is integrated with implantable cardiac devices. The system includes at least one sensory component that is adapted to measure one or more hemodynamic parameters inside a cardiac chamber of a subject. At least one transceiver is attached with the sensory component to transmit a signal containing data corresponding to the hemodynamic parameters and receive control signals from an external control device. An energy harvesting system is attached with the sensory component to measure pressures within the cardiac chamber and generate power for the monitoring system. The monitoring system can be attached with a heart valve or other cardiac device and implanted within a patient.

Abstract: The present invention satisfies the long felt need for a more compact and durable valve which may be formed in situ. The present invention provides a self-deployable valve system, a method of delivery, and a method of manufacturing for the self-deployable valve system. The present invention delivers the necessary components for forming a complete valve system in situ. The collapsed subcomponents of the system lack any functional characteristics commonly associated with a valve before being expanded. However, once expanded, the system is transformed into a competent valve for use in a wide variety of applications.

Abstract: An expandable stent that can transform between a collapsed state and an expanded state is described. The stent includes a first cross-sectional shape and a second cross-sectional shape. The first cross-sectional shape is a non-convex shape when the stent is in the collapsed state. Alternatively, the second cross-sectional shape is a convex shape when the stent is in an expanded state. The stent can be formed of super elastic Nitinol, which allows it to be shape set in the desired shape. Due to its shape setting properties and the non-convex cross-section, the stent is capable of dramatically reducing its cross-sectional radial profile which is beneficial in a variety of procedures.

Abstract: First and second structures are connected by helical fibers. The orientation between the first and second structures are changed, and by doing so, the positions of the helical fibers are correspondingly changed. The position of change of the helical fibers can be used for a pumping effect, or to change some other fluidic characteristics. One other fluidic characteristics, for example, may use the movement of the helical fibers as a valve.

Abstract: First and second structures are connected by helical fibers. The orientation between the first and second structures are changed, and by doing so, the positions of the helical fibers are correspondingly changed. The position of change of the helical fibers can be used for a pumping effect, or to change some other fluidic characteristics. One other fluidic characteristics, for example, may use the movement of the helical fibers as a valve.

Abstract: Described is a monolithic in situ forming valve system. The valve system is delivered in an unformed, collapsed configuration that lacks any functional characteristics commonly associated with a valve before. However, once expanded, the system is transformed into a competent valve for use in a wide variety of applications. The valve system includes a superior expandable structure, an inferior expandable structure, and a helical pre-valve component. The helical pre-valve component comprises a first end attached with the superior expandable structure and a second end attached with the inferior expandable structure. The helical pre-valve component is formed such that expansion of the superior expandable structure and the inferior expandable structure causes the helical pre-valve structure to transform into a functional valve held between each of the expandable structures.

Abstract: In accordance with certain embodiments of the present disclosure, a nursing bottle is provided. The bottle includes a body having a hollow interior and defining an upper opening. The bottle further includes a nipple joined to the body and disposed over the upper opening. The bottle also includes a means for generating negative pressure within a portion of the interior of the body.

Abstract: In accordance with one embodiment of the present disclosure, a method for deformation mapping of a tissue is provided. The method includes utilizing a device to measure transient three-dimensional deformations in a tissue sample. The device comprises a non-contacting, high-speed stereo imaging apparatus and a mechanism for digital image correlation. The method further includes identifying regions of the tissue that are prone to damage based upon the deformations.

Abstract: In accordance with certain embodiments of the present disclosure, a device for treatment of obesity in a patient is provided. The device comprises an inflatable material and a flexible ring-shaped member. The inflatable material is joined to the flexible ring-shaped member to define a space that is configured to be expanded when the device is inflated to a generally torus shape, the ring-shaped member defining an opening therethrough.

Abstract: In accordance with one embodiment of the present disclosure, a prosthetic valve is provided. The prosthetic valve includes an annulus, a pair of leaflets, and a pair of support elements. The annulus has a generally saddle-shape formed by a movable pair of first portions separated from each other by a movable pair of second portions. The pair of leaflets extend from the annulus and are separated from each other by the pair of support elements. The first portions of the annulus and the second portions of the annulus are configured to move back and forth from being generally concave to being generally convex such that any movement of the first portions of the annulus occurs at generally the same time as any movement of the second portions of the annulus.

Abstract: An implantable prosthetic valve that is transformable from a first helical pre-implantation configuration to a second valvular functional configuration, and methods of delivery.

Abstract: The present invention satisfies the long felt need for a more compact and durable valve which may be formed in situ. The present invention provides a self-deployable valve system, a method of delivery, and a method of manufacturing for the self-deployable valve system. The present invention delivers the necessary components for forming a complete valve system in situ. The collapsed subcomponents of the system lack any functional characteristics commonly associated with a valve before being expanded. However, once expanded, the system is transformed into a competent valve for use in a wide variety of applications.

Abstract: Described is a monolithic in situ forming valve system. The valve system is delivered in an unformed, collapsed configuration that lacks any functional characteristics commonly associated with a valve before. However, once expanded, the system is transformed into a competent valve for use in a wide variety of applications. The valve system includes a superior expandable structure, an inferior expandable structure, and a helical pre-valve component. The helical pre-valve component comprises a first end attached with the superior expandable structure and a second end attached with the inferior expandable structure. The helical pre-valve component is formed such that expansion of the superior expandable structure and the inferior expandable structure causes the helical pre-valve structure to transform into a functional valve held between each of the expandable structures.

Abstract: An implantable prosthetic valve that is transformable from a first helical pre-implantation configuration to a second valvular functional configuration, and methods of delivery.