A slit lamp and biomicroscope assembly can include a viewing system including a biomicroscope; an illumination system including a slit lamp with a light source and a light processing system with a first actuator; a positioning system supporting the biomicroscope and the slit lamp and including second and third actuators to position the biomicroscope along horizontal and vertical axes; and a user interface handle. The user interface handle can be graspable by a hand of a user and supported on the positioning system proximate to the biomicroscope such that a user looking into the biomicroscope can reach the user interface handle. The user interface handle can include a plurality of input devices including input devices in communication with the actuators.

An accommodating intraocular lens assembly can include a first lens, a first stanchion, a second lens, and a second stanchion. The first lens can have a first anterior side and a first posterior side. The first stanchion can have a first distal end connected to the first lens and a first base end. The second lens can have a second anterior side and a second posterior side. The second stanchion can have a second distal end connected to the second lens and a second base end. The first lens and the second lens can move laterally relative to one another during contraction of the ciliary muscle in a vertically-extending plane containing the optic axis of the eye and substantially centered in the eye.

A trephination apparatus can include a first member, a blade, and a second member. The first member can include a through-aperture and a first internal chamber. The first member can also include opening to the first internal chamber that can surround the through-aperture in a plane. The blade can have an outwardly-facing male profile at least partially matching the through-aperture and have a cutting edge. The second member can include a first body sized to be received in the through-aperture with the blade. The blade can be positionable between the first body and the female profile at the second opening. The second member can also include a second internal chamber with an opening extending about the aperture axis in the plane with an opening to the first internal chamber.

Disclosed are adjustable intraocular lenses and methods of adjusting intraocular lenses post-operatively. In one embodiment, an adjustable intraocular lens can comprise an optic portion and a peripheral portion. The peripheral portion can comprise a composite material comprising an energy absorbing constituent and a plurality of expandable components. A base power of the optic portion can be configured to change in response to an external energy directed at the composite material.

Disclosed are adjustable accommodating intraocular lenses and methods of adjusting accommodating intraocular lenses post-operatively. In one embodiment, an adjustable accommodating intraocular lens comprises an optic portion and a peripheral portion. At least one of the optic portion and the peripheral portion can be made in part of a composite material comprising an energy absorbing constituent and a plurality of expandable components. At least one of a base power and a cylindricity of the optic portion can be configured to change in response to an external energy directed at the composite material.

Embodiments disclosed herein generally relate to an intraocular drug delivery system configured for implantation into an eye of a subject. The intraocular drug delivery system can include an intraocular lens (IOL) and a drug delivery component. The IOL includes an anterior side, a posterior side opposite the anterior side, a lens bordered by an edge and a haptic extending outwardly from the edge of the lens at a lens-haptic junction. The haptic includes, at the lens-haptic junction, a relief cut on the posterior side of the IOL. The drug delivery component includes a therapeutic agent and a fixation portion having an opening configured to receive the haptic therethrough. The fixation portion is configured to be secured to the relief cut of the haptic such that outward movement of the drug delivery component relative to the lens is inhibited.

A system and method of treating target tissue in a patient's eye, which includes generating a light beam, deflecting the light beam using a scanner to form first and second treatment patterns, delivering the first treatment pattern to the target tissue to form an incision that provides access to an eye chamber of the patient's eye, and delivering the second treatment pattern to the target tissue to form a relaxation incision along or near limbus tissue or along corneal tissue anterior to the limbus tissue of the patient's eye to reduce astigmatism thereof.

An IOL system includes a capsular ring having a concave exterior surface extending around its circumference that is configured, upon insertion into a capsular bag of a patient's eye, to engage an equatorial region of the capsular bag. The concave exterior surface extends between an anterior surface and a posterior surface of the capsular ring. A first one or more flaps are arranged on the anterior surface such that at least a portion of each of the first one or more flaps, upon insertion into the capsular bag of a patient's eye, engages an anterior portion of the capsular bag. Similarly, a second one or more flaps are arranged on the posterior surface such that at least a portion of each of the second one or more flaps, upon insertion into a capsular bag of a patient's eye, engages a posterior portion of the capsular bag.

IOL of the type which include a lens, haptics and a curving ring wherein there are soft haptics and rigid haptics, both being associated through a lever and wherein a softer outer ring houses in its inner geometry an inner curving ring, the latter being rigid and incomplete, with curving flaps in whose geometry the assembly consisting of lens and haptics is housed.

An embodiment in accordance with the present invention provides a synthetic lens capsule for use in IOL fixation that is compatible with current and future IOL implants and relatively straightforward to implant. The device of the present invention can be inserted into the eye via a small (<3.0 mm) incision in the eye wall. The device of the present invention is compatible with all known or conceivable ways of securing the device to the eye. Securement is preferably done with at least two-point securement. In some embodiments, the device may also include a proprietary or conventional method of securement. To allow for expansion of the device as space permits, the device can also include a flexible ring structure. The device can include at least one aperture for the passage of light. The device of the present invention simplifies visual rehabilitation in cases of inadequate capsular support for IOL fixation.