Abstract: A wound cover device can include a backing, a micro-structure device, and one or more of a wound dressing and a skin replacement layer. The backing can be stretchable. The micro-structure device can include a plurality of fasteners, such as micro-staples, micro-pins, micro-barbs and the like, that can be used to attach the wound cover device to tissue such as skin. The micro-structure device can be stretchable to stretch with the backing. The micro-structure device can be configured such that the fasteners are positioned in a two-dimensional pattern or fill-in an interior portion of the wound dressing or skin replacement layer. The fasteners of the micro-structure device can extend through the wound dressing or skin replacement layer. The micro-structure device can additionally be placed around a perimeter or edge region of the backing.

Abstract: A wound closure device comprises a backing comprising a width configured to extend along at least a portion of a wound from a first end to a second end and a length configured to extend transversely across the wound, an adhesive layer coupled to the backing, a first micro-structure array attached to the backing proximate the first end, the first micro-structure array configured to extend transversely across the wound, a second micro-structure array attached to the backing proximate the second end, the second micro-structure array configured to extend transversely across the wound, and an elongate wound closure space between the first and second micro-structure arrays.

Abstract: A wound cover device can comprise a backing, a micro-structure device, and one or more of a wound dressing and a skin replacement layer. The backing can be stretchable The micro-structure device can comprise a plurality of fasteners, such as micro-staples, micro-pins, micro-barbs and the like, that can be used to attach the wound cover device to tissue such as skin. The micro-structure device can be stretchable to stretch with the backing. The micro-structure device can be configured such that the fasteners are positioned in a two-dimensional pattern or fill-in an interior portion of the wound dressing or skin replacement layer. The fasteners of the micro-structure device can extend through the wound dressing or skin replacement layer. The micro-structure device can additionally be placed around a perimeter or edge region of the backing.

Abstract: A comprehensive system (10) for the growing, analyzing, storing, validating and distributing of cells or tissues for a variety of purposes, in which the comprehensive system (10) generally uses a macrocontainer (12) for each of the steps from beginning to end. The macrocontainer (12) may include a number of elements, an essential one of which is the primary container (14). In every case, the primary container (14) includes a biosensor and a data registry device (15) (usually a microchip) to record and to display the handling history of the primary container (14) throughout the implementation of the system (10). The macrocontainer (14) provides process control, sterility and a matrix within and around which associated inlets, outlets and data lines may be coordinated.

Abstract: A comprehensive system (10) for the growing, analyzing, storing, validating and distributing of cells or tissues for a variety of purposes, in which the comprehensive system (10) generally uses a macrocontainer (12) for each of the steps from beginning to end. The macrocontainer (12) may include a number of elements, an essential one of which is the primary container (14). In every case, the primary container (14) includes a biosensor and a data registry device (15) (usually a microchip) to record and to display the handling history of the primary container (14) throughout the implementation of the system (10). The macrocontainer (14) provides process control, sterility and a matrix within and around which associated inlets, outlets and data lines may be coordinated.

Abstract: The present invention relates to methods for the use of T cells or supernatants therefrom, and more particularly, activated T cells, in facilitating and/or regulating the differentiation, de-differentiation, maturation, organization, repair, and regeneration of various cells/tissues. Methods for inducing tissue repair and regeneration in vitro and in vivo are disclosed. The present invention also relates to compositions of cells, including activated T cells and/or cells resulting from the co-culture with activated T cells, and their use in inducing tissue repair and regeneration in vivo.