Abstract: A method, computer program product, and computing system for receiving content from a third-party. The content may be processed to predict the disclosure of sensitive information. The sensitive information may be obscured from a platform user, where the third-party may be a customer and the platform user may be a customer service representative.

Abstract: A method, computer program product, and computing system for receiving content from a third-party; processing the content to predict the disclosure of sensitive information; and obscuring the sensitive information from a platform user.

Abstract: A glaucoma shunt (10) for reducing intraocular pressure (IOP) is provided. The glaucoma shunt (10, 50) includes a first planar element (12) from which extends a divider element (16). The first planar element (12) and the divider element (16) form two passageways (32) for aqueous evacuation.

Abstract: A flow regulating implant is provided with one or more grooves for allowing fluid flow. One or more grooves may have a constant or varying cross-section along its length. One or more grooves may have in it biodegradable material, absorbable material, and/or threads or sutures. A resilient band or coating may be placed around the implant or one or more grooves, to act as a pressure regulator. The implant may have a side projection, such as a side pin, for engaging tissue. The implant may comprise two or more parts that are held at a distance from each other to allow fluid flow between the parts.

Abstract: A flow regulating implant is provided with one or more grooves for allowing fluid flow. One or more grooves may have a constant or varying cross-section along its length. One or more grooves may have in it biodegradable material, absorbable material, and/or threads or sutures. A resilient band or coating may be placed around the implant or one or more grooves, to act as a pressure regulator. The implant may have a side projection, such as a side pin, for engaging tissue. The implant may comprise two or more parts that are held at a distance from each other to allow fluid flow between the parts.

Abstract: A flow regulating implant is provided with one or more grooves for allowing fluid flow. One or more grooves may have a constant or varying cross-section along its length. One or more grooves may have in it biodegradable material, absorbable material, and/or threads or sutures. A resilient band or coating may be placed around the implant or one or more grooves, to act as a pressure regulator. The implant may have a side projection, such as a side pin, for engaging tissue. The implant may comprise two or more parts that are held at a distance from each other to allow fluid flow between the parts.

Abstract: A glaucoma drain for non-penetrating deep sclerotorny is made of non-resorbable and hydrophilic synthetic material. The drain is configured to be entirely covered by the scleral flap and totally inserted in the intrascleral space. It comprises a transverse bar (110) at one front end of the drain and a longitudinal body (120) extending longitudinally from said transverse bar. The transverse bar (110, 10) is configured to run along and cover the Schlemm's canal (CS) and the opposite ends are configured to penetrate beneath the deep sclera inside the Sclernm's canal. A hole (125) between the arms of the bar provides a target for possible YAG laser micro-punctures.

Abstract: A flow regulating implant is provided with one or more grooves for allowing fluid flow. One or more grooves may have a constant or varying cross-section along its length. One or more grooves may have in it biodegradable material, absorbable material, and/or threads or sutures. A resilient band or coating may be placed around the implant or one or more grooves, to act as a pressure regulator. The implant may have a side projection, such as a side pin, for engaging tissue. The implant may comprise two or more parts that are held at a distance from each other to allow fluid flow between the parts.

Abstract: The invention concerns a glaucoma drain for non-penetrating deep sclerotomy, made of non-resorbable and hydrophilic synthetic material. The invention is characterised in that the drain is configured to be entirely covered by the scleral flap and totally inserted in the intrascleral space. It comprises a transverse bar (110) at one front end of the drain and a longitudinal body (120) extending longitudinally from said transverse bar. The transverse bar (110, 10) is configured to run along and cover the Schlemm's canal (CS) and the opposite ends are configured to penetrate beneath the deep sclera inside the Sclemm's canal. A hole (125) between the arms of the bar provides a target for possible YAG laser micro-punctures.

Abstract: A posterior chamber lens implant 10 formed of a soft material comprises a lens 12, a pair of flexible and resilient holding arms 14, 16 formed integrally with and projecting from the periphery of the lens 12 and lying in substantially the same plane as the lens 12, each arm 14, 16 having a first end 22 formed integrally with the lens 12 and a second end 24 distanced from the periphery of the lens 12, and a flexible web 18, 20 associated with each arm 14, 16 each web 18, 20 stretching between and being formed integrally with the periphery of the lens 12 and the second end 24 of its associated arm 14, 16. The webs 18, 20 are designed to hold the arms 14, 16 in position to prevent them flopping about during implantation and use of the lens implant 10. However, the webs 18, 20 are formed of a flexible material and thus it is possible to compress the arms 14, 16 towards the periphery of the lens 12 to assist in insertion of the lens implant 10 into the capsular bag or the ciliary sulcus of the eye.