196 results about "Phakic iol" patented technology

A method of designing a multifocal ophthalmic lens with one base focus and at least one additional focus, capable of reducing aberrations of the eye for at least one of the foci after its implantation, comprising the steps of: (i) characterizing at least one corneal surface as a mathematical model; (ii) calculating the resulting aberrations of said corneal surface(s) by employing said mathematical model; (iii) modelling the multifocal ophthalmic lens such that a wavefront arriving from an optical system comprising said lens and said at least one corneal surface obtains reduced aberrations for at least one of the foci. There is also disclosed a method of selecting a multifocal intraocular lens, a method of designing a multifocal ophthalmic lens based on corneal data from a group of patients, and a multifocal ophthalmic lens.

The present invention provides an ophthalmic lens capable of correcting or minimizing presbyopia, or of functioning used as an anti-myopic lens. The ophthalmic lens can be a contact lens, a phakic intraocular lens or an aphakic intraocular lens. The ophthalmic lens comprises an optical zone, the optical zone having a first surface and an opposite second surface and including a coma-like wavefront aberration oriented vertically from the top to the bottom of the ophthalmic lens. In addition, the present invention provides a method for minimizing/correcting presbyopia or for preventing children's eyes from becoming severely myopic.

An insertion device for an intraocular lens includes a lens-holding section having a cavity for accommodating an intraocular lens, a deforming section for deforming the lens to a reduced size, an insertion tube through which the deformed lens is inserted into an eye, a pusher mechanism for pushing and inserting the lens into the eye, and a lens-moving mechanism for moving the lens from a standby position to an insertion position at which the pusher mechanism can push and insert the lens into the eye. A lubricant is injected into the interior of the insertion tube and/or the cavity of the lens-holding section for smooth insertion of the lens. The insertion device has an indicating mark for indicating quantity of the injected lubricant. Further, the insertion device includes an erroneous operation prevention member for preventing accidental operation of the lens-moving mechanism.

An open chamber, accommodative, intraocular lens system operable to be positioned within an evacuated capsular bag of a human eye following extracapsular extraction of a natural crystalline lens is provided having an anterior refractive lens optic, a first haptic segment having a first end and being connected at said first end to a peripheral portion of said anterior lens optic and a second end and said haptic segment extending in an elliptical curve, in longitudinal cross-section, and at least a second haptic segment having a first end and being connected at said first end to a peripheral portion of said lens optic and a second end and said at least a second haptic segment extending in an elliptical curve, in longitudinal cross-section, and being operably joined with the second end of said first haptic segment to form an open chamber, elliptical shaped haptic accommodating support for the anterior lens within an evacuated capsular bag of a human eye.

Polysiloxanes suitable for the preparation of intraocular lenses by a crosslinking reaction, having a specific gravity of greater than about 1.0, a refractive index suitable for restoring the refractive power of the natural crystalline lens and a viscosity suitable for injection through a standard cannula are provided. Moreover, injectable intraocular lens material based on these polysiloxanes and methods of preparing intraocular lenses by direct injection into the capsular bag of the eye are also disclosed.

An intraocular lens having an anterior lens member (48) presenting an anterior light-converging optic (52) and a posterior lens member (50) presenting a posterior light-diverging optic (68) for magnifying an observed image onto large regions of the retina (32) to permit central focus in patients suffering from AMD and a method of implanting the lens into the human eye (10). The anterior light-converging optic (52) is operably coupled with a flexible body (58) which extends radially therefrom and presents opposing bights (62) presenting termini (66) when the lens is viewed in cross-section. The posterior light-diverging optic (68) is operably coupled with an annular flange (76) which is arcuate in cross-section and mates with termini. Both the anterior and the posterior lens members (48, 50) have positioning holes (70, 80) formed therein permitting surgical implantation thereof. The IOL (46) is constructed of a flexible synthetic resin material such as polymethylmethacrylate and permits focusing upon objects located near to and far from the viewer.

An ophthalmic method for determining a relationship between aphakic ocular power and estimated effective lens position (ELP) of an intraocular lens (IOL) to be implanted in a patient's eye. The method can be used to determine an estimate of the ELP of an IOL given the aphakic ocular power of the patient's eye, for example, without measurement of the corneal curvature or axial length of the patient's eye. The estimate of ELP can then be used to determine a suitable value of optical power for the IOL to be implanted in the patient's eye.

Provided herein are a devices, ophthalmic lens systems and methods for restoring natural tension and anatomy of a lens capsule post-surgically in an eye of a subject. The device generally comprises an inward tensioning ring-like structure having a shape configured to circumferentially fit within and be anchored to a post-surgical lens capsule of the eye. The device may have one or both of external and internal grooves formed to receive the lens capsule and one or both of an intraoptical lens or a tensioning element. The ophthalmic lens system generally comprises the device and an intraocular lens inserted therein. The anchored device provides tension to an equatorial area of the capsule resulting in a decrease in equatorial diameter.

An insertion device is used to deform a deformable intraocular lens to a reduced size and insert the deformed lens into an eye through an insertion tube. The insertion device includes a push rod for pushing and inserting the lens into the eye, and a posture control member disengagably engaged with a tip end portion of the push rod. The posture control member prevents deflection of the push rod from a center axis. The engagement between the posture control member and the push rod is broken when the push rod arrives at a predetermined position during a step of advancing the push rod.

Modular IOL removal systems and methods that cut an optic portion of an intraocular in a single motion such to facilitate removal of the optic portion from an eye through an incision, for example a corneal incision, without increasing the size of the corneal incision. Various cutting tools having one or more blades may be utilized. The cut intraocular lens may have one continuous cut or be cut into multiple smaller pieces. The single cutting step may apply balanced forces and torque to avoid damaging the surrounding eye anatomy, reducing the risk of trauma.

Intraocular lenses (IOLs) that improve lens stability by, for example, increasing anterior-posterior stiffness of the IOL, increasing anterior-posterior dimensions of the IOL and/or increasing contact area with the equator of the bag to resist movement of the IOL as the bag collapses over time. These IOLs may be non-modular (single component) or modular (multiple component). In modular embodiments, the IOL system may include intraocular base and optic components, which, when combined, form a modular IOL.

Modular IOL systems including a base and a lens, wherein the lens includes tabs for connection to the base. The modular IOL allows for the lens to be adjusted or exchanged while leaving the base in place, either intra-operatively or post-operatively.

An insertion device can deform a deformable intraocular lens into a smaller size and insert the intraocular lens into the eye. The insertion device includes a device body; an insertion tube attached to a front end of the device body and adapted to be inserted into the eye; and a push rod axially movable within the device body and the insertion tube and adapted to insert the intraocular lens into the eye when advanced. A drive member is rotatably provided at a rear end of the push rod. A motion conversion mechanism is disposed between the device body and the drive member and is adapted to axially move the drive member, upon rotation of the drive member, in order to axially move the push rod. A push member is provided at the rear end of the push rod and projects rearward from the drive member.

An intraocular lens insertion device capable of folding an intraocular lens into a predetermined shape without giving a local stress to the intraocular lens. The intraocular lens insertion device 2 includes a lens disposing part 15 for disposing an intraocular lens 4, a slider 7 for pushing out the intraocular lens 4, a plunger 8 for further pushing out the intraocular lens pushed out by the slider 7, a transition part 31 for deforming the intraocular lens 4 pushed out by the slider and the plunger, and a nozzle 32 for ejecting out the deformed intraocular lens 4. The slider 7 includes a lens push-out part 47 having a larger contact area than the plunger 8 and a lens holder 52 holding one face of an optical part 4b of the intraocular lens 4 in one direction. The transition part 31 deforms a portion of an outer edge of the intraocular lens 4 parallel to the lens traveling direction in an other direction opposite to the one direction.

An apparatus and method for reducing intraocular pressure in a patient's eye is provided. A deformable intraocular member having a relaxed state with a relaxed profile having a first width, a first energized state with a first profile having a second width, and a second energized state with a second profile having a third width is provided. The deformable intraocular member relaxed state width is greater than the width of a lens capsule which surrounds a lens of the patient's eye prior to cataract surgery. The second energized state width is greater than the patient's lens capsule width after cataract surgery and smaller than the width in the relaxed state. The deformable intraocular member in the second energized state is configured to urge deformation of the lens capsule to thereby promote opening of a trabecular meshwork and canal of Schlemm of the patient's eye to promote drainage of aqueous humor from an anterior chamber and reduce intraocular pressure in the patient's eye.

An intraocular lens insertion device comprises a pad formed by an elastic element harmless to a living body, a drawing thread mounted on a rear portion of the pad, and an insert portion formed at a front portion of the pad. The insert portion has a shape suitable to fit into a ciliary sulcus of an aphakic eye. The pad has a thickness capable of covering a tip end of a surgical needle.

This relates to a lens made of donor corneal tissue suitable for use as a contact lens or an implanted lens, to a method of preparing that lens, and to a technique of placing the lens on the eye. The lens is made of donor corneal tissue that is acellularized by removing native epithelium and keratocytes. These cells optionally are replaced with human epithelium and keratocytes to form a lens that has a structural anatomy similar to human cornea. The ocular lens may be used to correct conditions such as astigmatism, myopia, aphakia, and presbyopia.

There is disclosed herein a “piggyback” cylindrical (toric) intraocular lens for placement in front of an accommodating or standard intraocular lens that is already in the capsular bag of the eye. This additional lens is placed in the sulcus, which leaves a significant space between the two lenses, particularly if the lens in the capsular bag is vaulted backwards.

An intraocular lens for modifying the refractive abilities of a natural lens or an existing artificial lens in an eye to correct for vision disorders such as presbyopia, myopia, hyperopia or astigmatism. Specifically, the lens system can be configured so that it does not effect far vision, while effecting near vision using a plus lens to correct for presbyopia. The lens system includes a lens portion and fastening members, with the lens portion being movably secured to at least one of the fastening members so that the position of the lens portion can be modified with respect to the optical axis, and the overall length of the lens system can be increased or decreased.