In embodiments, a light adjustable lens irradiation system for a light adjustable lens irradiation system, comprises an irradiation light source, for generating a UV light beam; an optical system, for directing the UV light beam towards a light adjustable intraocular lens, implanted into an eye of a patient; and a patient interface, coupled to the optical system, for stabilizing the eye relative to the optical system, to achieve an alignment of the light adjustable intraocular lens and the UV light beam.

To improve the precision of ophthalmic surgical procedures by reducing corneal wrinkling, a patient interface for an ophthalmic system can include an attachment portion, configured to attach the patient interface to a distal end of the ophthalmic system; a contact portion, configured to dock the patient interface to an eye; and a contact element, coupled to the contact portion, configured to contact a surface of a cornea of the eye as part of the docking of the patient interface to the eye, and having a central portion with a central radius of curvature Rc and a peripheral portion with a peripheral radius of curvature Rp, wherein Rc is smaller than Rp.

An orbital tissue retractor 10 for use in a surgical operation in the region of an eye socket, comprises an orbital tissue retractor body 12 and a handle 14 extending therefrom for manipulation of the tissue retractor body by a surgeon. The tissue retractor body comprises a channel formation 16 defining a channel 17. The channel formation 16 has a pair of spaced side wall sections 24 which define concave curved ocular abutment formations 26 which conform to an anatomical curvature of the ocular globe for abutment with the ocular globe N. The tissue retractor body has open proximal end 22 and an open distal end 20. The tissue retractor body tapers from the proximal end to the distal end, with a portion of the channel formation at the distal end being curved so as to accommodate and cradle the optic nerve therein. The retractor body has a curved base wall section 28 conforming to an anatomical curvature of the orbit.

Methods, devices, and systems are presented for inserting an implant in the cornea of the eye, where the implant is a microshunt; a microshunt delivery device for delivering the microshunt into the cornea may comprise the microshunt, an actuator, and a suction stabilizer; a vacuum device may be inserted in the stabilizer such that the cornea may be sucked onto a concave bottom side of the stabilizer; the microshunt may then be inserted into a hole in the suction stabilizer with the actuator; the actuator may be turned to screw the microshunt into a hole in the cornea; and the actuator may be removed from the suction stabilizer, breaking the vacuum seal and leaving the microshunt inserted in the cornea.

A laser eye surgery system produces a treatment beam that includes a plurality of laser pulses. An optical coherence tomography (OCT) subsystem produces a source beam used to locate one or more structures of an eye. The OCT subsystem is used to sense the distance between a camera objective on the underside of the laser eye surgery system and the patient's eye. Control electronics compare the sensed distance with a pre-determined target distance, and reposition a movable patient support toward or away the camera objective until the sensed distance is at the pre-determined target distance. A subsequent measurement dependent upon the spacing between the camera objective and the patient's eye is performed, such as determining the astigmatic axis by observing the reflection of a plurality of point source LEDs arranged in concentric rings off the eye.

A shunt 10 for implantation in the human body for treating ocular disorders related to disorders of intraocular or intracranial pressure by providing for flow of aqueous fluid in the anterior chamber A of the eye and cerebrospinal fluid in the subarachnoid space B surrounding the optic nerve C. The shunt has a proximal end 12 which is implanted in the ocular anterior chamber and a distal end 14 which is implanted in the subarachnoid space. The shunt has a two-part construction, including a flexible distal tube 18 and a rigid proximal tube 20. The distal tube has a distal stop formation 26 near the distal end 14 which is located in the subarachnoid space upon implantation of the distal end, resisting withdrawal of the shunt. The proximal tube has a curved portion which conforms to the anatomical curvature of the ocular globe.

To improve the precision of ophthalmic surgical procedures by reducing corneal wrinkling, a patient interface for an ophthalmic system can include an attachment portion, configured to attach the patient interface to a distal end of the ophthalmic system; a contact portion, configured to dock the patient interface to an eye; and a contact element, coupled to the contact portion, configured to contact a surface of a cornea of the eye as part of the docking of the patient interface to the eye, and having a central portion with a central radius of curvature Rc and a peripheral portion with a peripheral radius of curvature Rp, wherein Rc is smaller than Rp.

In embodiments, a light adjustable lens irradiation system for a light adjustable lens irradiation system, comprises an irradiation light source, for generating a UV light beam; an optical system, for directing the UV light beam towards a light adjustable intraocular lens, implanted into an eye of a patient; and a patient interface, coupled to the optical system, for stabilizing the eye relative to the optical system, to achieve an alignment of the light adjustable intraocular lens and the UV light beam.

A laser eye surgery system that has a patient interface between the eye and the laser system relying on suction to hold the interface to the eye. The patient interface may be a liquid-filled interface, with liquid used as a transmission medium for the laser. During a laser procedure various inputs are monitored to detect a leak. The inputs may include a video feed of the eye looking for air bubbles in the liquid medium, the force sensors on the patient interface that detect patient movement, and vacuum sensors directly sensing the level of suction between the patient interface and the eye. The method may include combining three monitoring activities with a Bayesian algorithm that computes the probabilities of an imminent vacuum loss event.

A non-sliding, non-sutured hands-free contact lens assembly for ophthalmic procedures utilizes a number of microstructures strategically placed on the bottom of either the contact lens or the bottom of a contact lens holder ring. After the contact lens, or the contact lens assembled with the contact lens holder ring, is placed on the cornea of the eye and centered, a surgeon applies downward pressure either on the contact lens itself or on the lens holder ring. This secures the lens assembly to the cornea due to increased friction between the microstructures and the tissues of the eye when the microstructures penetrate through the tear film and, optionally, viscous solution film and into the contact with superficial layer of cornea or other parts of the eye, thus temporarily anchoring the contact lens, or lens holder, to the desired surgical site.