Glaucoma Treatment Device
First Claim
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1. An ocular treatment device, comprising:
- an inflow port near a proximal end region configured to be in fluid communication with the anterior chamber of an eye;
an outflow port near a distal end region;
a fluid flow pathway communicating between the inflow port and the outflow port;
a plurality of openings in the distal end region extending through a wall of the device and communicating with the fluid flow pathway; and
a plurality of retention features in the distal end region surrounding the wall of the device,wherein the device has an outer contour defined by a first radius of curvature of the proximal end region and a second radius of curvature of the distal end region, wherein the second radius of curvature is tighter than the first radius of curvature such that the proximal end region is directed away from a region of the cornea when the device is implanted in the eye.
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Abstract
Methods and devices are adapted for implanting into the eye. An incision is formed in the cornea of the eye and a shunt is inserted through the incision into the anterior chamber of the eye. The shunt includes a fluid passageway. The shunt is passed along a pathway from the anterior chamber through the scleral spur of the eye into the suprachoroidal space and positioned in a first position such that a first portion of the fluid passageway communicates with the anterior chamber and a second portion of the fluid passageway communicates with the suprachoroidal space to provide a fluid passageway between the suprachoroidal space and the anterior chamber.
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Citations
12 Claims
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1. An ocular treatment device, comprising:
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an inflow port near a proximal end region configured to be in fluid communication with the anterior chamber of an eye; an outflow port near a distal end region; a fluid flow pathway communicating between the inflow port and the outflow port; a plurality of openings in the distal end region extending through a wall of the device and communicating with the fluid flow pathway; and a plurality of retention features in the distal end region surrounding the wall of the device, wherein the device has an outer contour defined by a first radius of curvature of the proximal end region and a second radius of curvature of the distal end region, wherein the second radius of curvature is tighter than the first radius of curvature such that the proximal end region is directed away from a region of the cornea when the device is implanted in the eye. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12)
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Specification