Abstract: An intraocular lens implantable in an eye includes an optic for placement in the capsular bag of the eye and for directing light toward the retina of the eye. The optic has a central optical axis, an anterior face, an opposing posterior face and a peripheral edge between the faces. The peripheral edge has one or more curved or angled surfaces that reduce glare within the IOL. For instance, a rounded transition surface on the anterior side of the peripheral edge diffuses the intensity of reflected light, or a particular arrangement of straight edge surfaces refracts the light so as not to reflect, or does not reflect at all. The intersection of the peripheral edge and at least one of the anterior face and the posterior face, preferably both of such faces, forms a peripheral corner located at a discontinuity between the peripheral edge and the intersecting face or faces.

Abstract: Methods of producing an intraocular lens in vivo comprise preparing a composition of discrete water soluble macromolecular particles, mixing the composition with a water soluble photoinitiator and forming an opthalmically acceptable aqueous solution having a refractive index of at least 1.39, injecting the resulting aqueous solution into the capsular bag of an eye, and initiating crosslinking between the macromolecular particles by irradiation of a wavelength in the range of about 380 to 700 nm to create a lens in the capsular bag.

Abstract: A handpiece system for multiple phacoemulsification procedures is provided which includes a housing having a distal end adapted for sealably and releasably engaging a plurality of nose cones and a sonic generator disposed within the housing. A horn having a body connected to the sonic generator and a needle is provided for radiating sonic energy into an eye for fragmenting eye tissue. A plurality of nose cones are provided which are adapted for being sealably and releasably engaged with the housing and provide structure enabling varied phacoemulsification procedures.

Abstract: An intraocular lens system includes a primary intraocular lens configured to correct vision in a patient, and a supplemental intraocular lens configured to modify the correction provided by the primary intraocular lens. The supplemental intraocular lens, which is substantially completely diffractive, is preferably ultrathin. The two lenses may be connected to, or separate from, one another. The supplemental intraocular lens may be implanted at the same time as the primary intraocular lens, or added later.

Abstract: According to the invention the ophthalmic lens further comprises a refractive part comprising at least one surface, which is configured to compensate a passing wavefront at least partly for at least one type of monochromatic aberration introduced by at least one of the optical parts of the eye. Said diffractive part is capable of compensating a passing wavefront at least partly for chromatic aberration introduced by at least one of the optical parts of the eye. Furthermore said refractive and diffractive parts together contribute to a required power of the lens.

Abstract: An binocular lens system for improving the vision of a patient including first and second ophthalmic lenses. Each of these lenses is adapted for implantation in an eye or to be disposed on or in the cornea. The first lens has a first baseline diopter power for distance vision correction and the second ophthalmic lens has a second baseline diopter power for other than distance vision correction. The ophthalmic lenses may be intraocular lenses which are implanted in the eyes of a patient or has natural lenses or following removal of the natural lenses.

Abstract: An intraocular lens system including one or more intraocular lenses (IOL) and a peripheral holder. The peripheral holder is configured to receive and retain the distal end of a fixation member of the IOL and provide a dynamic interface between the natural capsular bag and fixation member. The holder is preferably annular and flexible and transmits movement of the capsular bag from the surrounding ciliary muscles to the IOL. In this manner, a circumferential surface contact with the capsular bag is provided and accommodation of the IOL is improved. If two IOLs are received in the holder, a spacer may be provided to insure consistent spacing between the IOLs. Alternatively, an IOL system may include two IOLs and a spacer, without the holder. The holder desirably includes a sharp exterior corner to inhibit cell growth and posterior capsular opacification.

Abstract: A foldable intraocular lens (IOL) includes an optic and at least one fixation member for supporting the optic in the anterior chamber of an eye. The fixation member includes an intermediate portion that extends a first direction away from the optic, and a leg portion that intersects with an outer end of the intermediate portion and extends a second direction, different from the first direction, away from the outer end. The leg portion preferably includes a reduced width region near the intersection with the intermediate portion. The reduced width region acts essentially as a hinge allowing the leg portion to flex about the intermediate portion in responsive to compressive forces, while the intermediate portion and optic remain stable.

Abstract: An intraocular lens for use in a mammalian eye having a natural lens, the intraocular lens including a lens body sized and adapted for placement in the eye, and having a baseline optical power and at least one optical add power. The at least one optical add power is reduced relative to the corresponding optical power of a similar intraocular lens adapted for placement in a similar eye in which the natural lens has been removed.

Abstract: A novel ophthalmic viscosurgical system and method is disclosed. The system and method comprise multiple viscoelastic solutions that are pre-selected based on desired characteristics. Each solution is placed in distinct locations within the eye during surgery to maintain the natural shape of the eye and facilitate the surgical procedure. Novel viscoelastic solutions for use in association with the present invention are also disclosed.

Abstract: Apparatus for the removal of intraocular tissue from an eye includes an unsleeved vibrated needle insertable through a first eye incision into the intraocular tissue for emulsifying same. The needle is ultrasonically vibrated for emulsifying the intraocular tissue in a manner preventing substantial heat damage to the eye and a combined aspiration/irrigation needle or separate aspiration and irrigation needles are provided for both introducing irrigation fluid into the eye and aspirating emulsified intraocular tissue and irrigation fluid from the eye.

Abstract: An intraocular lens includes an optic adapted to focus light toward a retina of an eye, and at least one fixation member configured to at least assist in supporting the optic in the eye. The fixation member includes a proximal portion coupled to the optic and a distal portion configured to be in contact with eye tissue when the intraocular lens is in use in the eye. The proximal portion of the fixation member includes at least one first area formed of a first, substantially rigid material, and at least one second area formed of a second material which is more flexible than the first material.

Abstract: A multi-purpose contact lens care solution comprising taurine, a liquid aqueous medium, an antimicrobial component, a surfactant and a buffer. This solution prevents losses in ocular tissue membrane integrity during contact lens wear.

Abstract: An accommodating IOL comprises an optic adapted to focus light toward a retina of an eye, and a movement assembly coupled to the eye to provide effective accommodating movement, preferably axial movement, of the optic. At least a portion of the movement assembly is made from a material that is less stiff and/or more resilient than the material used to make the optic. Optionally, an outer ring or support portion made at least partially from either a relatively stiff material such as the material used in the optic or a relatively resilient material such as the material used in the movement assembly is also provided.

Abstract: Apparatus for measuring accommodation of a lens in an eye includes a target, a Badal lens, and a viewing aperture, where the Badal lens and the viewing aperture are positioned so that when the target moves towards or away from the lens, the apparent size of the target remains constant to a subject looking in the viewing aperture regardless of the distance the target moves. The apparatus may be provided in a compact housing and may include a mirror placed in the housing so that the viewing aperture can be placed away from the optical axis of the lens. The apparatus includes a controller to control the movement of the target. The apparatus measures the accommodation of a lens based on the distance the target moves during an examination. Methods of measuring accommodation of a lens in an eye of a subject are also disclosed.

Abstract: Test apparatus for bi-manual phaco needle apparatus are provided which includes a chamber for establishing a fluidic circuit between an irrigation needle and an aspiration needle. A first inlet into the chamber is provided for establishing a sealed communication with the irrigation needle and a second inlet is provided for establishing a sealed fluid communication with an aspiration needle. The apparatus enables a method for testing bi-manual phacoemulsification apparatus and priming thereof.

Abstract: An intraocular lens (IOL) insertion apparatus for implanting acrylic IOLs through smaller incisions. The insertion apparatus includes an insertion cartridge that receives the IOL and cooperates with a handpiece. The cartridge includes a longitudinal lumen from a loading chamber to an open distal mouth that gradually narrows in dimension so as to fold the acrylic IOL to a dimension of less than about 2.0 mm. The cartridge is made of a polymer, such as polypropylene, that includes a lubricity enhancing component concentrated at surfaces by a blooming process. A push rod in the handpiece enters the loading chamber of the cartridge and urges the IOL therethrough. A distal tip of the push rod has an irregular shape, such as a rounded trapezoidal, and has a maximum dimension slightly less than the inner diameter of the open distal mouth of the cartridge. The distal tip of the push rod may have a relief channel on one side that accommodates a trailing haptic of the IOL.

Abstract: A partially hydrated lens is provided for implantation into a cornea. The partially hydrated lens has a water content less than the water content of the cornea, resulting in an osmotic pressure differential between the lens and the cornea which improves adhesion between the lens and the corneal tissue. It also causes the lens to expand and flatten when implanted, and to [naturally center itself while flattening.] In the preferred embodiment of the invention, the lens is maintained in its partially hydrated state by storage in a hypertonic hydration medium.

Abstract: Apparatus for inserting intraocular lenses (IOLs) into eyes are disclosed. The apparatus comprises an insertion tube, and an injector rod having a distal tip capable of engaging an intraocular lens. A guide assembly is provided to direct the distal tip of the rod radially outwardly as it moves distally through the insertion tube. The radial movement of the tip is controlled such that the tip contacts a proximal edge, rather than a fold, of the IOL. The tip exerts little or no pressure on the bottom wall of the IOL cartridge, with any incidental pressure varying as the tip moves distally. In one embodiment, the guide assembly also includes a component for allowing the tip to return upward after contacting the IOL, thus decreasing or eliminating the pressure on the wall as the rod tip continues through a narrower diameter exit portion of the cartridge. Methods for inserting an IOL into an eye using such apparatus are also disclosed and are within the scope of the present invention.

Abstract: An iris-supported intraocular lens having an optic portion and a plurality of fixation members coupled thereto. Each fixation member has a pair of pincer arms that separate outward of the optic and converge toward one another at aligned end tips. One or both of the end tips are covered with a soft sleeve or cap. The IOL is fixed in the anterior chamber of the eye by pinching the iris tissue between the end tips of each pair of pincer arms. The soft sleeves eliminate damage to the iris tissue.