Abstract: A processing subsystem generates perceived images from information bearing nerve impulses that are transmitted from a subject's eye(s) to a visual processing region of the subject's brain along one or more nerves in response to the subject viewing a real-world scene. The processing subsystem generates display images based on the perceived images, and controls a display device to display the display images to the subject. In certain embodiments, the processing subsystem generates the display images by manipulating or modifying the perceived images to include virtual images, and provides a type of virtual pointing on the display images that is used to invoke one or more actions.

Abstract: A processing device receives signals associated with nerve impulses that are transmitted to the visual cortex of a subject in response to one or more visual stimuli provided to at least one eye of the subject. The processing device processes the received signals and generates digital image data from the processed received signals that is representative of the visual perception, by the subject, of the one or more visual stimuli. In certain embodiments, the processing device processes digital image data that is representative of a scene to convert the digital image data to a sequence of nerve impulses, and provides the sequence of nerve impulses to the visual cortex of a subject such that the subject visually perceives the scene.

Abstract: A patient simulator system includes a right eye assembly including a right eyelid and a right pupil, and a left eye assembly including a left eyelid and a left pupil, wherein the right pupil moves within an area of the right eye and the left pupil moves within an area of the left eye. In various embodiments, right/left optical sensors provide right/left electrical signals based on sensed light conditions associated with the right/left eyes, and a microprocessor changes a size of the right iris based on the right electrical signal, and changes a size of the left iris based on the left electrical signal. In various embodiments, the microprocessor electrically actuates at least one blink motor to rotate, wherein rotation of the at least one blink motor results in motion of the right eyelid and/or the left eyelid to simulate blinking.

Abstract: Systems and methods involving an intraocular implant with input and/or output electronics are described. In some embodiments, the system includes an intraocular lens having at least one optic operably coupled to a haptic, one or more input electronics on the haptic and/or the optic; and one or more output electronics on the haptic and/or the optic for receiving and/or transmitting data.

Abstract: Disclosed are devices, methods and systems for treatment of eye disease such as glaucoma. Implants are described herein that enhance aqueous flow through the normal outflow system of the eye with minimal to no complications. The implant can be reversibly deformed to a first shape, such as a generally linear shape conducive to insertion. Upon insertion, the implant can deform to a second shape, such as a generally non-linear shape conducive to retention within the eye. The shape also improves fluid flow from the anterior chamber and prevents or reduces clogging.

Abstract: A method of reducing the risk of macular degeneration is provided. The method includes inserting an intraocular collar stent into a portion of a mammalian eye, such that the stent is in contact with soft tissue of the anterior chamber. When inserted in the eye, the stent applies pressure to a surface centered on a transition zone, between an anterior limit of a trabecular meshwork and a posterior limit of a corneal endothelium of the eye, to a surface of the peripheral iris of the eye, and in circumferentially expanding direction to the irideocorneal angle. The pressure is applied continually. The method also includes creating an environment of a reduced negative pressure state within the retina as a result of the application of the pressure; and, while the reduced negative pressure state is present, permitting drusen precursors formed by extracellular material to flow through the eye for removal by vasculature of the eye.

Abstract: A simulated eye is provided for taxidermy, replica animals made by carving wood, modeling, and other replica animal or replica human construction. The simulated eye provides a more realistic appearance than previous simulated eyes. The eye includes a domed central portion resembling a cornea that is surrounded by a scleral band. The eye is made from one-piece construction using materials that simulate the refractive index of a natural eye. The interior of the eyes are painted to resemble the iris and pupil of a real eye. The configuration of the simulated eye, in conjunction with the refractive index of the material with which it is made, provides a realistic appearance as the angle at which the eye is viewed changes. The eye is structured for easy mounting.

Abstract: An adjustable apparatus for stabilizing an eyeball suitable for use during surgical or transplant procedures is disclosed. Furthermore, an associated method is also provided.

Abstract: A intravitreous stent includes a multi-loop single wire having a proximal end; a distal end; at least a first loop defined by the proximal end and a first portion of the single wire; at least a second loop defined by the distal end and a second portion of the single wire; wherein the first portion is joined to the second portion via a reversing loop portion.

Abstract: An animatronic eye with fluid suspension, electromagnetic drive, and video capability. The eye assembly includes a spherical, hollow outer shell that contains a suspension liquid. An inner sphere is positioned in the outer shell in the suspension liquid to be centrally floated at a distance away from the shell wall. The inner sphere includes painted portions providing a sclera and iris and includes an unpainted rear portion and front portion or pupil. The shell, liquid, and inner sphere are have matching indices of refraction such that interfaces between the components are not readily observed. A camera is provided adjacent a rear portion of the outer shell to receive light passing through the shell, liquid, and inner sphere. A drive assembly is provided including permanent magnets on the inner sphere that are driven by electromagnetic coils on the outer shell to provide frictionless yaw and pitch movements simulating eye movements.

Abstract: There is described a novel orbital implant having a smooth but macroporous outer surface, the said implant containing an integral resorbable platform for guided ocular muscle re-attachment.

Abstract: A method of manufacturing an artificial eye for fitting as a whole or partial replacement of a patient's original eye, the method comprising the steps of: a) providing a digitally acquired image of an iris; and b) transferring the image to a substrate comprising at least the frontal region of an artificial eye.

Abstract: A replica eye includes a dome-shaped eyeball, a back simulating member, a front simulating member, a container, at least one tube, and a driving member. The eyeball includes a light-transmitting area for transmitting light. The back simulating member has a simulating surface being a first color. The front simulating member has a resilient capsule being a second color other than the first color. The resilient capsule is attached to the simulating surface, and arranged between the simulating surface and the light-transmitting area. The container is used for accommodating fillers. The at least one tube is capable of passing through the simulating surface to connect between the resilient capsule and the container. The driving member is coupled to the container for driving the fillers received in the container move towards and away from resilient capsule via the tube.

Abstract: An ocular implant adapted to reside at least partially in a portion of Schlemm's canal of an eye. In some embodiments the implant has a body extending in a curved volume whose longitudinal axis forms an arc of a circle, and a plurality of open areas and strut areas formed in the body, the open areas extending over more than 50% of a surface defining the curved volume, the strut areas surrounding the open areas, the body having a diameter of between 0.005 inches and 0.04 inches. The invention also provides a method of treating glaucoma including the steps of supporting tissue forming Schlemm's canal in an eye with an implant extending at least partially in the canal along an axial length within the canal; and contacting with the implant less than 50% of the tissue forming the canal along the axial length.

Abstract: Glaucoma treatments utilizing an implanted shunt having an elastomeric plate and a non-valved elastomeric drainage tube. The plate is positioned over a sclera of the eye with an outflow end of the elastomeric drainage tube open to an outer surface of the plate. An inflow end of the drainage tube tunnels through tissue to the anterior chamber of the eye. The drainage tube collapses upon insertion within an incision in the sclera and cornea, or at a kink on the outside of the incision, but has sufficient resiliency to restore its patency over time. Delayed fluid communication between the outflow and inflow ends of the drainage tube permits a scar tissue bleb to form around the plate. The plate desirably has a peripheral ridge and fenestrations, and a longer suturing tab extending from one side of the plate to enhance visibility and accessibility when suturing the shunt to the sclera.

Abstract: An ocular prosthesis includes a posterior sclera portion partially nested with an anterior clear portion. An iris disk piece and/or a retinal chip may also be disposed between the posterior and anterior portions. A method for manufacturing the ocular prosthesis includes scanning an impression of an eye socket or an existing ocular prosthesis, fabricating posterior and anterior portions from geometrical models generated from the scans, and forming the ocular prosthesis by joining the two portions. In another embodiment of the method, a photograph of an iris is provided and manipulated to form a multi disk iris piece to be used in the ocular prosthesis.

Abstract: A toy eye includes a casing having a transparent top portion, a lens defining a through hole, and a pupil received in through hole of the lens. The lens and the pupil are both made of soft resilient material, and clung to the transparent top portion of the casing. The toy eye also includes a push-pull element for pushing the pupil towards the transparent top portion of the casing or pulling the pupil reversely. The toy eye further includes a light processing element for sensing the change of the outside light intensity and generating a driving signal when the value of the change of the light intensity reaches or exceeds a predetermined value, and a driving element for driving the push-pull element to push or pull the pupil, upon receiving the driving signal from the light processing element.

Abstract: An ocular implant for treating glaucoma is provided, which may include any number of features. More particularly, the present invention relates to implants that facilitate the transfer of fluid from within one area of the eye to another area of the eye. One feature of the implant is that it includes a proximal inlet portion and a distal inlet portion adapted to be inserted into the anterior chamber of the eye, and an intermediate portion adapted to be inserted into Schlemm's canal. Another feature of the implant is that it can be biased to assume a predetermined shape to aid in placement within the eye.

Abstract: A coating for an orbital implant where the coating has an anterior portion having a different, longer term bioabsorbability than a posterior portion. This allows the implant to have a smooth surface for insertion and to provide reduced irritation to neighboring tissues, to help prevent exposure of the porous core of the implant, and to provide a stable anchorment for extraocular muscles, but which also encourages rapid fibrovascular ingrowth. The coating is marked with a visual indicator to facilitate proper orientation. Shell materials are further selected to allow for sterile packaging, the securing of therapeutic agents thereon, and to provide adequately strong securing of the coating to the core. Apertures are formed through the coating to enhance fluid flow to and from the core, and to provide exposure of the surface of the core to extraocular muscles, and for sutures. The apertures are sized and shaped to reduce irritating surface contact with orbital tissues.

Abstract: Devices and methods for treating intraocular pressure are disclosed. The devices include drug delivery implants for treating ocular tissue. Optionally, the devices also include shunts for draining aqueous humor from the anterior chamber to the uveoscleral outflow pathway, including the supraciliary space and the suprachoroidal space. The drug delivery implants can be implanted in ab interno or ab externo procedures.

Abstract: An ocular implant having a first spine; a second spine; a first strut extending in an axial direction Z between the first spine and the second spine; a second strut extending in an axial direction Z between the first spine and the second spine; wherein an angular dimension ? of a first edge of each strut undulates as the strut extends in the axial direction Z between the first spine and the second spine; and wherein a radius r of an outer surface of each strut remains substantially constant as the strut extends the axial direction Z between the first spine and the second spine.

Abstract: A replica eye includes an eyeball with a light-transmitting area for transmitting light, a resilient film, a driving member, and a transmission mechanism. The resilient film includes a pupil portion and an iris portion surrounding the pupil portion. The pupil portion is in a first color. The iris portion is in a second color other than the first color. The driving member has a shaft. The driving member provides rotating forces to the shaft. The transmission mechanism comprises a rotor fastened on the shaft of the driving member, and a plurality of flexible members in radial arrangement. A first end of each flexible member away from the rotor is fastened on an outer edge of the resilient film. When the driving member rotates the transmission mechanism, centrifugal forces are imparted on the plurality of flexible members, the plurality of flexible members stretches the pupil portion and the iris portion.

Abstract: A coating for an orbital implant where the coating has an anterior portion having a different, longer term bioabsorbability than a posterior portion. This allows the implant to have a smooth surface for insertion and to provide reduced irritation to neighboring tissues, to help prevent exposure of the porous core of the implant, and to provide a stable anchorment for extraocular muscles, but which also encourages rapid fibrovascular ingrowth. The coating is marked with a visual indicator to facilitate proper orientation. Shell materials are further selected to allow for sterile packaging, the securing of therapeutic agents thereon, and to provide adequately strong securing of the coating to the core. Apertures are formed through the coating to enhance fluid flow to and from the core, and to provide exposure of the surface of the core to extraocular muscles, and for sutures. The apertures are sized and shaped to reduce irritating surface contact with orbital tissues.

Abstract: A prosthetic device and method to restore extraocular muscle function. The device includes a housing; a biasing component disposed in the housing; a proximal connector operatively connected to a proximal end of the biasing component; and a distal connector operatively connected to a distal end of the biasing component, wherein the proximal connector is configured for being secured with respect to an orbital bone and the distal connector adapted to be secured to the paralyzed or absent muscle stump, e.g. on the globe, or to the eyelid.

Abstract: A replica eye includes a dome-shaped eyeball, a back simulating member, a front simulating member, a container, at least one tube, and a driving member. The eyeball includes a light-transmitting area for transmitting light. The back simulating member has a simulating surface being a first color. The front simulating member has a resilient capsule being a second color other than the first color. The resilient capsule is attached to the simulating surface, and arranged between the simulating surface and the light-transmitting area. The container is used for accommodating fillers. The at least one tube is capable of passing through the simulating surface to connect between the resilient capsule and the container. The driving member is coupled to the container for driving the fillers received in the container move towards and away from resilient capsule via the tube.

Abstract: A quasi-spherical orbital implant that comprises an off center conical elongation toward its posterior and medial aspects. The conical elongation mimics the natural shape of an orbit. The implant comprises a number of holes and tunnels for suturing the patient's eye muscles and tissue to the implant. A number of hollow voids in the implant serve to progressively host the formation of tissue which secures the implant to the muscles and covering tissue and helps to prevent migration after the sutures have dissolved. The anterior portion of the implant has a number of details which key with the prosthetic eye and help improve its stability and motility.

Abstract: A prosthetic eye with an iris constructed of a photoresponsive, polymer based element. The photoresponsive element is responsive to light, so that the pupils constrict in the presence of light. The responsiveness of the pupils to light gives the prosthetic eye a more natural appearance.

Abstract: One example scleral prosthesis includes a first free end and a second free end, each wider than a middle portion of the scleral prosthesis. Multiple first portions form the first end of the scleral prosthesis. The first portions are separated along at least half of a length of the scleral prosthesis. Multiple second portions may form the second end of the scleral prosthesis, and the second portions may be separated along less than a quarter of the length of the scleral prosthesis. An implantation device can be used to facilitate implantation of a scleral prosthesis. The implantation device includes a first end portion configured to be inserted into a scleral tunnel of an eye. The implantation device also includes a second end portion configured to receive the scleral prosthesis. A rod with a tapered and rounded end can be partially inserted into the first end portion of the implantation device.

Abstract: An animatronic eye with fluid suspension, electromagnetic drive, and video capability. The eye assembly includes a spherical, hollow outer shell that contains a suspension liquid. An inner sphere is positioned in the outer shell in the suspension liquid to be centrally floated at a distance away from the shell wall. The inner sphere includes painted portions providing a sclera and iris and includes an unpainted rear portion and front portion or pupil. The shell, liquid, and inner sphere are have matching indices of refraction such that interfaces between the components are not readily observed. A camera is provided adjacent a rear portion of the outer shell to receive light passing through the shell, liquid, and inner sphere. A drive assembly is provided including permanent magnets on the inner sphere that are driven by electromagnetic coils on the outer shell to provide frictionless yaw and pitch movements simulating eye movements.

Abstract: Systems and methods are described for implanting a device in a mammalian eye to raise intraocular pressure. In some embodiments, the device (54) includes an arcuate body that, when implanted, obstructs aqueous humor outflow from the anterior chamber (38) of the eye.

Abstract: The present invention relates to a foldable capsular vitreous body (FCVB), and its mould design, method for manufacturing, product appearance, and drug delivery property and so on. A mould for molding a foldable artificial vitreous body comprises an upper mould (1), a lower mould (2) and a core (3). The core (3) is disposed between the upper mould (1) and the lower mould (2) and is connected with a drainage-tube pin connected with an injection channel (4). Heating holes (6) are disposed in the upper mould (1) and/or the lower mould (2). Material is injected to the mould and is heated to vulcanize to mold vitreous body. The FCVB is adapted to be injected with any harmless medium and can be used as a delivery vehicle inside or around the eye ball. The size or shape of the FCVB can be changed depending on the different implant site.

Abstract: A prosthetic device and method to restore extraocular muscle function. The device includes a housing; a biasing component disposed in the housing; a proximal connector operatively connected to a proximal end of the biasing component; and a distal connector operatively connected to a distal end of the biasing component, wherein the proximal connector is configured for being secured with respect to an orbital bone and the distal connector adapted to be secured to the paralyzed or absent muscle stump, e.g. on the globe, or to the eyelid.

Abstract: A reading enhancement device for preventing and/or treating presbyopia of the eye. The enhancement device is sutured to an outer wall of the sclera for buckling and compressing a portion of the sclera and the ciliary body inwardly and perpendicular to the plane of the sclera and exerting a posterior compression force toward the vitreous humor in the rear of the eye. The enhancement device includes a compression body with a front of the body having semi-circular convex surface. The convex surface is used for engaging, buckling and compressing both a portion of the sclera and the ciliary body of the eye. The compression body also includes an enlarged, rounded first and second end portions and an elongated center portion with the convex surface formed thereon. Also, the compression body includes a rear having an outwardly extending rib portion with a pair of grooves at opposite ends of the rib portion.

Abstract: According to an embodiment of the present invention, an implant device may be provided. The implant may be adapted to manipulate the position of an eyeball associated with a patient, whereby the device comprises an insertion device including a first and a second portion. The first portion may include a first thickness and may be adapted to elevate the position of the eyeball. The second portion may include a second thickness and/or a second position relative the first portion for moving the position of the eyeball in a forward direction.

Abstract: An artificial eye includes a supporter, a first clipping member, a second clipping member and an electroactive pupil. The second clipping member is positioned on the supporter. A peripheral portion of the second clipping member is positioned on a peripheral portion of the first clipping member. A gap is defined between the first and second clipping members. The electroactive pupil is positioned in the gap and contacts the first and second clipping members.

Abstract: A coating for an orbital implant where the coating has an anterior portion having a different, longer term bioabsorbability than a posterior portion. This allows the implant to have a smooth surface for insertion and to provide reduced irritation to neighboring tissues, to help prevent exposure of the porous core of the implant, and to provide a stable anchorment for extraocular muscles, but which also encourages rapid fibrovascular ingrowth. The coating is marked with a visual indicator to facilitate proper orientation. Shell materials are further selected to allow for sterile packaging, the securing of therapeutic agents thereon, and to provide adequately strong securing of the coating to the core. Apertures are formed through the coating to enhance fluid flow to and from the core, and to provide exposure of the surface of the core to extraocular muscles, and for sutures. The apertures are sized and shaped to reduce irritating surface contact with orbital tissues.

Abstract: The present invention relates to a bio-artificial eye which is produced by a process comprising adding loess, zeolite, bentonite, bioceramic or nano-silver to acrylic resin powder. Thus, the artificial eye has antibacterial activity in itself, does not cause much eye discharge, and emits far-infrared rays and anions, and thus, has a very good effect on the ocular health of a person wearing the artificial eye. Furthermore, the present invention relates to a conformer which is produced by a process comprising adding loess, zeolite, bentonite, bioceramic or nano-silver to acrylic resin powder. Thus, the inventive conformer has antibacterial activity in itself, does not cause much eye discharge, and emits far-infrared rays and anions, and thus, has a very good effect on the ocular health of a person wearing the conformer.

Abstract: There is described a novel orbital implant having a smooth but macroporous outer surface, the said implant containing an integral resorbable platform for guided ocular muscle re-attachment.

Abstract: An artificial eye socket for use in the mounting of artificial eye is disclosed. The artificial eye socket is of substantially unitary construction and made from a flexible material such as rubber. The artificial eye socket comprises an outer base surface; an inner base surface; a substantially contiguous outer sclera surface which extends from the outer base surface to an iris knife edge to and from an iris opening in said socket; and a substantially contiguous inner cavity surface which extends from said inner base surface to said iris knife edge to form said iris opening in said socket and a cavity within said socket. An artificial eye may be inserted into said cavity and secured in a substantially fixed position by the inner base surface and the cavity surface. Methods for manufacturing and mounting the artificial eye socket and cleaning the surface of the artificial eye are also disclosed.

Abstract: A coating for an orbital implant where the coating has an anterior portion having a different, longer term bioabsorbability than a posterior portion. This allows the implant to have a smooth surface for insertion and to provide reduced irritation to neighboring tissues, to help prevent exposure of the porous core of the implant, and to provide a stable anchorment for extraocular muscles, but which also encourages rapid fibrovascular ingrowth. The coating is marked with a visual indicator to facilitate proper orientation. Shell materials are further selected to allow for sterile packaging, the securing of therapeutic agents thereon, and to provide adequately strong securing of the coating to the core. Apertures are formed through the coating to enhance fluid flow to and from the core, and to provide exposure of the surface of the core to extraocular muscles, and for sutures. The apertures are sized and shaped to reduce irritating surface contact with orbital tissues.

Abstract: A vision prosthesis includes an optical element having a surface that is shaped to be positioned near a cornea of an eye, and a magnetic element embedded in the optical element.

Abstract: A system for generating visual images includes an artificial eye that is surgically implanted within a patient's orbit. Also, the system includes a micro-camera that is mounted to the artificial eye for capturing visual input. A digital signal processor receives the visual input from the micro-camera and generates electrical stimuli corresponding to pixels of the visual input. In the system, a plurality of electrode arrays are embedded into selected areas of the primary visual cortex of the patient. Further, each array is interconnected with the processor to transfer the electrical stimuli to predetermined areas of the primary visual cortex for creation of a visual image by the patient corresponding to the visual input.

Abstract: A prosthetic eye with an iris constructed of a photoresponsive, polymer based element. The photoresponsive element is responsive to light, so that the pupils constrict in the presence of light. The responsiveness of the pupils to light gives the prosthetic eye a more natural appearance.

Abstract: The present invention provides a silicone-based ocular prosthesis. In one aspect, the prosthesis includes a posterior sclera portion fabricated from a white-tinted silicone material. The sclera portion is formed from a molding process. The prosthesis also includes an anterior iris portion placed on the sclera portion. The prosthesis further includes a transparent layer over the sclera portion and the iris portion to provide a protective coating, and depth to the eye. Finally, a clear coat finish may optionally be applied to the prosthesis to create a realistic, wet look. A method for making the silicone-based ocular prosthesis using a molding process is also provided herein.

Abstract: According to an embodiment of the present invention, an implant device may be provided. The implant may be adapted to manipulate the position of an eyeball associated with a patient, whereby the device comprises an insertion device including a first and a second portion. The first portion may include a first thickness and may be adapted to elevate the position of the eyeball. The second portion may include a second thickness and/or a second position relative the first portion for moving the position of the eyeball in a forward direction.

Abstract: The present invention is a flexible ocular restraint band that includes a thin flexible material such as a surgical mesh fabric with flexible reinforced end portions. The device is positioned posterior to the eye globe and the reinforced ends are sutured to anterior portions of the scleral ring. Preferably, a side edge of the band is formed with a concave curved edge to be placed proximate the optical nerve without making contact or applying pressure to the optical nerve. When properly positioned the device prevents further axial elongation of the eye. In alternative embodiments the band may be formed as a generally linear strap, a three legged or “Y” shaped strap or a four legged “X” shaped strap.

Abstract: A method of performing intra-articular therapy and a dilution resistant viscoelastic composition are disclosed. One embodiment of the dilution resistant composition comprises a hyaluronate-based viscoelastic agent and a low viscosity, polymer-containing solution. The hyaluronate-based viscoelastic can be an aqueous solution sodium hyaluronate having an average molecular weight greater than 750,000 Daltons and a concentration by weight between 0.5% and 3%. The polymer-containing solution can contain a polymer selected from the group consisting of chondroitin sulfate and hydroxypropylmethylcellulose. One embodiment can comprise a polymer-containing solution containing hydroxypropylmethylcellulose at a concentration by weight from about 0.05% to about 5.0% and chondroitin sulfate at a concentration by weight from about 0.1 to about 7%.

Abstract: Scleral implants are provided having structure that locks the implant into incisions in the sclera and provide a stress thereto. In several embodiments, such structure includes a foot that extends laterally from a bottom of the implant, as well as an opening through which suture may be passed. Furthermore, the foot of the implant may be contoured to conform to the natural curvature of the sclera. In other embodiments, the implant is generally disc-shaped and includes a tab and a suture opening. With this implant, one or two pockets are defined in the sclera, preferably at eleven o'clock and/or one o'clock, the implant is placed therein, and the pocket incision may be closed with suture. The implant may also include a system for measuring and transmitting the intraocular pressure. With all the implants, the eye pressure is increased and/or the sclera is lifted to treat a disorder of the eye.

Abstract: Scleral implants are provided having structure that locks the implant into incisions in the sclera and provide a stress thereto. In several embodiments, such structure includes a foot that extends laterally from a bottom of the implant, as well as an opening through which suture may be passed. Furthermore, the foot of the implant may be contoured to conform to the natural curvature of the sclera. In other embodiments, the implant is generally disc-shaped and includes a tab and a suture opening. With this implant, one or two pockets are defined in the sclera, preferably at eleven o'clock and/or one o'clock, the implant is placed therein, and the pocket incision may be closed with suture. The implant may also include a system for measuring and transmitting the intraocular pressure. With all the implants, the eye pressure is increased and/or the sclera is lifted to treat a disorder of the eye.

Abstract: Scleral implants are provided having structure that locks the implant into incisions in the sclera and provide a stress thereto. In several embodiments, such structure includes a foot that extends laterally from a bottom of the implant, as well as an opening through which suture may be passed. Furthermore, the foot of the implant may be contoured to conform to the natural curvature of the sclera. In other embodiments, the implant is generally disc-shaped and includes a tab and a suture opening. With this implant, one or two pockets are defined in the sclera, preferably at eleven o'clock and/or one o'clock, the implant is placed therein, and the pocket incision may be closed with suture. The implant may also include a system for measuring and transmitting the intraocular pressure. With all the implants, the eye pressure is increased and/or the sclera is lifted to treat a disorder of the eye.