Abstract: An intraocular lens injector cartridge assembly contains a pre-loaded lens and an integral lens-contacting plunger rod. Configured for removably mating with an injector handpiece, the cartridge assembly is suitable for use with either manual or automated injector systems. The injector cartridge assembly includes a tubular body having a longitudinal bore extending between a distal end and a proximal end, an IOL disposed within said longitudinal bore, and a lens-contacting plunger rod retained within said bore, between the IOL and the proximal end of the tubular body. The lens-contacting plunger rod is configured for translation along the longitudinal bore upon engagement by an injector rod introduced by the injector handpiece into the proximal end of the tubular body, so that the IOL is folded and ejected from the distal end of the tubular body by the translation of the lens-contacting plunger rod.

Abstract: An exchangeable intraocular lens device having a flexible, high-memory expansile lens fixation platform adapted to receive the haptics of an intraocular lens, and their method of use, are provided. The device is specifically designed to expand completely into the equatorial fornix of the capsular bag and become permanently implanted therein. The design of the present invention addresses the desire of patients to exchange their existing intraocular lens to meet their changing visual needs or to take advantage of improved lens technology, without incurring the significant risks typically associated with exchange of current intraocular lens technology. The exchangeable intraocular lens device provides accurate centration, positioning, and stability of the intraocular lens in the capsular bag. The exchangeable intraocular lens device reduces lens epithelial cell migration and resultant posterior capsule opacification.

Abstract: An improved cutter assembly is used to form an aperture in a lens capsule of an eye. The cutter assembly is resiliently deflectable between a contracted condition and an expanded condition. When the cutter assembly is in the contracted condition, it is moved through an opening in the eye into alignment with an anterior portion of lens capsule of the eye. The cutter assembly is then operated to the expanded condition and moved against the anterior portion of the lens capsule under the influence of fluid pressure. To move the cutter assembly against the anterior portion of the lens capsule, a seal engages an anterior portion of the lens capsule and a conduit connected with the cutter assembly is connected in fluid communication with a source of low pressure (vacuum).

Abstract: 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.

Abstract: An intraocular injector includes a syringe body having open-ended cone disposed in one end thereof along with a piston disposed in the body. A transparent implant holder having a lumen therein is aligned with an open-ended cone, a needle include a proximal end and a distal end with a bevel disposed on the distal end of the needle. A plunger affixed to the piston and slidable within a holder lumen and needle lumen is provided for injecting solid intraocular implants into an eye. A cylindrical syringe body shape facilitates control over the needle bevel orientation during injection of the implant into the eye.

Abstract: A liquefaction surgical handpiece having a check valve within the boiling chamber. Such a construction reduces upstream fluid volume. Reduction of upstream fluid volume reduces capability for compliance caused either by trapped air or absorbed gas in the liquid.

Abstract: An apparatus and methods for delivering ocular implants or microimplants. The apparatus is ergonomically designed for ease of use, and a simple manual depression of an actuator produces proportional movement of a linkage causing the implant or microimplant to be ejected through a cannula disposed at the desired location in the eye. Small gauge cannulas are provided for self-sealing methods of delivery.

Abstract: A tool configured to prepare a dual-optic accommodating intraocular lens for implantation can comprise a first portion and a second portion. The first portion can comprise a base and at least one elongate guide associated with the base. The first portion can be in contact with and not movable relative to a first optic of the lens during at least a portion of the preparation of the lens. The a second portion can comprise an actuator having an engagement surface in contact with a second optic of the lens and at least one protrusion extending away from the engagement surface. The protrusion can be configured to extend into engagement with the elongate guide. The first and second portions can be movable relative to each other as permitted by the guide(s) and protrusion(s) to move the optics so that the lens takes on a more compact condition for implantation.

Abstract: There is disclosed an accommodating intraocular lens for implantation in an eye having an optical axis. The lens comprises an anterior portion which in turn comprises an anterior viewing element and an anterior biasing element. The lens further comprises a posterior portion which in turn comprises a posterior viewing element in spaced relationship to the anterior viewing element and a posterior biasing element. The anterior portion and posterior portion meet at first and second apices of the intraocular lens. The anterior portion and the posterior portion and/or the apices are responsive to force thereon to cause the separation between the viewing elements to change. Additional embodiments and methods are also disclosed.

Abstract: Provided is an intraocular lens insertion device capable of omitting a repeated operation after the intraocular lens is inserted into the eye. The intraocular lens insertion device (1) comprises a lens setting part (11) for mounting an intraocular lens (5) having an optic (6) and one or two or more supporting portions (7a and 7b) disposed at the outer edge of the optic (6), a plunger (4) for pushing out the intraocular lens (5) mounted in the lens setting part (11), and a nozzle (13) for releasing the intraocular lens (5) pushed out by the plunger (4). This plunger (4) includes a lens contact portion (32) for abutting against the outer edge of the optic (6), and a pushing portion (33) for pushing out the supporting portion (7b) arranged in the backward direction of a lens advancing axis (A).

Abstract: An intraocular lens injection device comprises a tubular housing with a passageway extending along its longitudinal axis and a plunger shaft disposed within and moveable along the passageway. The tubular housing and the plunger shaft have frictional engaging features that are configured to produce a varying plunging friction as the plunger is moved along its operating range, to offset changes in the plunging resistance that arise from injecting the IOL into the eye. The variable plunging friction may comprise one or more step changes in unloaded plunging friction, or a curved variation in plunging friction, or both, along at least a portion of the operating range of the plunger shaft. In some embodiments, a slot of varying width in the housing frictionally engages a tab extending transversely from the plunger shaft. In others, a contoured surface on the plunger shaft frictionally engages an orifice in the tubular housing.

Abstract: A device for inserting an intraocular lens (IOL) into an eye includes a tubular body member with an inner surface and a plunger with an gripping device that is receivable within the body member. The gripping device includes a locking member and is configured such that when urged longitudinally in a distal direction, the gripping device is movable in the distal direction within the body member. However, when urged longitudinally in a proximal direction, the gripping device is prevented from moving in the proximal direction by the locking member engaging with the inner surface of the body member. As such, inadvertent movement of the plunger in the proximal direction caused by pulling back on the plunger is substantially prevented. If proximal movement of the plunger is desired, then the plunger may include handle that is operatively coupled to the gripping device such rotation of the handle causes the handle to move longitudinally in the body member.

Abstract: A grafting reagent and related method of using the reagent to form a polymeric layer on a support surface, and particularly a porous support surface, in a manner that provides and/or preserves desired properties (such as porosity) of the surface. The reagent and method can be used to provide a thin, conformable, uniform, uncrosslinked coating having desired properties onto the surface of a preformed, and particularly a porous, polymeric substrate.

Abstract: A method of eliminating post-excitation vibration provided from a surgical handpiece to a patient's eye during ophthalmic surgery. The surgical handpiece includes an ultrasonic vibration structure for generating vibration and a needle for transmitting the vibration into the patients eye. The method includes exciting the ultrasonic vibration structure and thereby causing the needle to vibrate for emulsifying tissue in the patient's eye, ceasing the excitation of the crystal structure, and generating a brake signal to restrain the vibration of the needle, upon ceasing the excitation of the crystal structure, thereby reducing the vibration provided to the patient's eye after excitation of the crystal structure has ceased.

Abstract: The invention relates to a method for producing a surgical micromanipulator tip including a proximal mounting base, at least a first elbow, and a distal manipulator finger. The elbow is connected to the mounting base and terminates at the free end of the tip. In addition, the mounting base includes at least one distal segment. The first elbow and the manipulator finger together form a tip portion. The tip portion is uniformly tapered by pointing.

Abstract: An intraocular lens insertion tool of a novel structure, capable of easily and reliably placing an intraocular lens in a human eye. A placement part (20) formed communicated with the base end (74) of an insertion tube part (70) is formed in a tool body (12). A placement surface (30) for placing an intraocular lens (26) thereon is formed on the placement part (20). Through-holes (66, 68) are formed in the portion where the placement surface (30) is formed, and a carrying member (50) is assembled from the outside to the portion where the placement surface (30) is formed. Support parts (56, 58) formed projected from the carrying member (50) are projected from the support surface (30) through the through-holes (66, 68). The intraocular lens (26) is supported by projecting distal end faces (61, 64) of the support parts (56, 58).

Abstract: An ophthalmic surgery system for wirelessly supplying power to at least one surgical module during ophthalmic surgery. The ophthalmic surgery system includes a power module having a power transmitter configured to generate an electromagnetic field in at least a space proximal to the power module, a surgical module including a power receiver, and a surgical console in communication with the surgical module. Power is wirelessly induced in the power receiver when the surgical module is within the space, such that at least one component included in the surgical module is substantially powered by the induced power.

Abstract: IOL injector system and method for injecting an IOL into an eye which incorporates the benefits of both a rigid and soft plunger tip lens engagement surface while at the same time reduces or eliminates the disadvantages associated therewith.

Abstract: An intraocular lens (IOL) delivery device is disclosed. The device includes an intraocular lens cartridge having an internal coating wherein the coating includes a polymeric material that is compatible with a polymeric material of a material that forms the cartridge. Preferably, the polymeric material of the coating, the cartridge or both is a polyurethane material.

Abstract: A vacuum sealing devices (10) used for surgical procedures, particularly on the eye. The device (10) comprises a flexible sleeve (11) which terminates in a platter (11a) having a sealing suction ring (12, 112, 212). The suction ring (12, 112, 212) couples the sleeve (11) to the body and isolates the surgical site from surrounding tissue. The sleeve (11) may be provided with a opening (22, 113) which allows instrumentation access through and incision such as a corneal incision (13).

Abstract: The present invention is directed to the provision of an intraocular lens delivery device having a plunger with a multi-part plunger tip. The plunger tip includes a first part and a second part wherein the first part releases from the second part during travel of the plunger through the body of a delivery cartridge.

Abstract: A method of preventing rejection of an implant in the eye, includes forming a flap in the cornea of the eye, inserting an implant under the flap, cross linking corneal tissue surrounding an implant to make the corneal tissue surrounding an implant less vulnerable to enzymatic degradation, inserting polymeric material under the corneal flap so as to overlie corneal tissue, compressing a layer of the cornea from outside using a lens having a predetermined curvature to correct refractive error of the cornea, and cross linking corneal tissue that the polymeric material overlies.

Abstract: Disclosed are devices and methods for the transfer of fluids and potentially toxic chemicals into the lens capsule by creating a closed system preventing the fluids from entering the anterior chamber of the eye and thus causing damage to other ocular structures. The invention comprises one or more fluid conduits which communicate with a plug which maybe inserted through the corneal incision and placed onto the anterior surface of the capsule around the capsulorhexis. The plug is adapted to seal against the anterior surface of the lens capsule. In preferred embodiments, the flow of fluids into and out of the plug (and therefore the capsule) are controlled from a separate fluid flow controller.

Abstract: An embodiment of an injector for an intraocular lens includes an injector body having a longitudinal axis. The body includes a first housing configured to receive the lens and a second housing configured to move relative to the first housing in the direction of the longitudinal axis. The injector also includes a lens engagement surface configured to engage a first, but not a second, viewing element of the lens. The injector includes opposing lens compaction members configured to move from a first position in which the lens compaction surfaces are spaced from each other to a second position in which the lens compaction surfaces are closer to each other and in which a lens positioned therebetween is compacted. In response to relative longitudinal movement of the housings, the lens engagement surface displaces the first viewing element from the second viewing element in the direction of the longitudinal axis, and the opposing lens compaction surfaces move from the first position to the second position.

Abstract: An intraocular lens injection system comprising an injecting device and cartridge. The cartridge comprises a lens holding portion and an outer sleeve portion. The invention includes a method of pre-loading the injecting system, particularly the cartridge, to reduce the amount of packaging, prevent damage to the intraocular lens during packaging and shipping, allow the pre-loaded injecting cartridge to be autoclaved as a unit, and eliminate the step of loading the cartridge with the intraocular lens by the end user to prevent potential damage during this step.

Abstract: Embodiments of the present invention provide an intraocular lens with an optic zone having a first surface topology and a haptic zone having a second surface topology. The surface roughness of the haptic zone may be greater than the surface roughness of the optic zone. The surface topology of the optic zone may have a first surface geometry and the surface topology of the haptic zone may have a second surface geometry. The first and second surface geometries may retain lubrication fluid in a space formed therein. The haptics formed by the manufacturing process may have a reduced ability to adhere to the optic zone, such as when the lens is folded or advanced through a cannula.

Abstract: An intraocular lens injection device comprises a tubular housing with a plunger longitudinally disposed within the tubular housing. An electric drive system longitudinally translates the plunger so that its tip engages an insertion cartridge to fold and displace an intraocular lens disposed within and to inject the folded lens into the lens capsule of an eye. A control circuit is configured to start translation of the plunger, responsive to user input, to detect at least one fault condition based on a counter-electromotive force produced by the electric motor, and to stop translation of the plunger assembly responsive to the detected fault condition, which may comprise excessive resistance to forward or rearward translation of the plunger or insufficient resistance to forward translation of the plunger.

Abstract: An IOL injector, comprising an injector body, a plunger and a plunger collar. The injector body has a lumen wall defining a lumen, a port through which a lens is inserted into a loading bay of the lumen, a stop, and an opening adapted for delivery of an IOL into an eye. The plunger comprising a plunger body, a plunger shaft and a plunger tip. The collar comprises a hole or a channel, the plunger shaft extending therethrough. The plunger shaft is slidably, frictionally engaged with the collar. The plunger and the collar are arranged within the lumen such that an outer surface of the collar can smoothly slide within the lumen wall from a first location where the tip is proximal of an IOL disposed at the loading bay to a second location where the stop interferes with the collar. The collar having an outer dimension that is substantially equal to a dimension of the lumen.

Abstract: A cartridge for an intraocular implant includes a loading chamber and an injection chamber communicating in a proximal portion of the cartridge. The cartridge further includes a piston chamber including a zone for communication with the loading chamber in a distal portion of the cartridge. The piston chamber includes a piston with an actuation end arranged to penetrate the loading chamber and to urge an intraocular implant located in the loading chamber through the injection chamber. An intraocular implant injector can include such a cartridge.

Abstract: The insertion device (2) includes a main body (3) including a lens housing portion (3b) in which an intraocular lens (1) is housed and an insertion cylindrical portion (3a) for ejecting the lens into the eye through its front end opening (3j), a pushing shaft (4) configured to move the lens from the lens housing portion to push out the lens into the eye through the insertion cylindrical portion, and a liquid flow path (10) configured to cause liquid filled in an inside of the main body to flow from the inside of the main body to an outside thereof, the liquid flow path not including the front end opening (3j). The pushing shaft includes a structure configured to shut off the liquid flow path after the lens is ejected from the front end opening and thereby flow of the liquid through the front end opening is allowed.

Abstract: A system of modifying an intraocular device located within an eye, wherein the system includes a laser assembly and a controller coupled to the laser assembly. The laser assembly outputs a pulsed laser beam having a pulse width between about 300 picoseconds and about 10 femtoseconds, and the controller directs the laser assembly to output the pulsed laser beam into the intraocular device. One or more slip zones are formed within the intraocular device in response thereto, and the slip zones are configured to modify a refractive profile of the intraocular device. A method of modifying a refractive profile of an eye having an intraocular device implanted therein, wherein the method includes determining a corrected refractive profile for the eye based on an initial refractive profile, identifying one or more locations within the intraocular device based on the corrected refractive profile, and directing a pulsed laser beam at the locations to produce the corrected refractive profile.

Abstract: Apparatus, and methods of making and using apparatus, for inserting intraocular lenses (IOLs) are disclosed. The apparatus includes a hollow tube having an interior wall defining a hollow space through which an intraocular lens may be passed from the open space into an eye. A lubricity enhancing component is covalently bonded to the hollow tube at the interior wall in an amount effective to facilitate the passage of the intraocular lens through the hollow space. The lubricity enhancing component includes a substituent component effective to reduce hydrolysis of said lubricity enhancing component relative to an identical lubricity enhancing component without the substituent component.

Abstract: Disclosed is an injector which comprises an injector housing having a longitudinal axis and an injection probe disposed along the longitudinal axis. The injector further comprises an intraocular lens disposed in the housing. The intraocular lens comprises first and second interconnected viewing elements, and the optical axes of the first and second viewing elements are substantially aligned. The optical axes are substantially orthogonal to the longitudinal axis of the housing. The injector further comprises a lens carrier which engages one of the viewing elements. The viewing elements are moveable in response to longitudinal movement of the lens carrier relative to the injector housing. The longitudinal movement causes both (i) the optical axes to be displaced relative to each other and (ii) the viewing elements to be disposed substantially on the longitudinal axis of the injector housing.

Abstract: The insertion device (2) for inserting an intraocular lens (1) into an eye includes a main body (12) including a lens housing portion (12b) in which the lens is housed and a nozzle portion (12c) for ejecting the lens into the eye, a pushing shaft (16) moving the lens from the lens housing portion and pushes out the lens into the eye through a front end opening (12j) of the nozzle portion, a first flow path configured to cause liquid to flow between the front end opening of the nozzle portion and an opening other than the front end opening, and a second flow path configured to cause liquid to flow between a portion (30a) protruding from the front end opening of the nozzle portion and an outside of the insertion device.

Abstract: A system comprising a hollow member is used to deliver a constrained corneal implant into a corneal pocket. The hollow member may be tapered and the system may further include an implant deformation chamber and an axial pusher to advance the implant through the hollow member.

Abstract: Twin bore ophthalmologic tubing includes first and second tubes. The second tube has portions of differing hardness with one of the portions being at an end of that tube. The second tube has a portion at its other end with about the same hardness. Portions of the first and the second tubes may have about the same hardness. In some embodiments, portions of the first and second tubes with the same hardness can correspond to each other along the tubing. One of the portions can have a hardness of 80 to 90 shore A while the other portion can be 60 to 70 shore A. In some embodiments, portions with 60 to 70 shore A hardness can be about six to twelve inches long.

Abstract: A reduction of eye trauma is achieved during opthalmolic surgery branch for implanting the intraocular refractive lens to the anterior chamber of the eye. The pupil is extended by mydriatic compounds and after anesthesia the cornea cut is made (clear cornea—3 mm). Thereafter, the anterior chamber of the eye is filled with viscoelastic compound with low molecular weight and then the refractive lens is implanted with the help of said cannula, the working face of the cannula at the middle between the lens edge and the border of the optic area, with the edge bent on the cannula face. The end by the top of the bending the refractive lens is introduced into the cornea cut and set in the posterior chamber of the eye. Thereafter, vacuum is removed and the cannula is detached from the refractive lens, and taken off the anterior chamber of the eye by the reverse movement. The refractive lens cannula is made as a tube with round or oval cross-section with inner diameter 0.5-2.5 mm and wall thickness not less than 0.

Abstract: A forceps for gripping an intraocular lens (IOL) has first and second jaws moveable toward on another. One jaw is formed with a first curvature and the remaining jaw is formed with a second curvature complementary to the first. When an IOL is gripped between the jaws, the first and second curvatures act to partially curve or fold the IOL, facilitating the insertion of the IOL into an IOL cartridge.

Abstract: [PROBLEMS] To provide an injector for ophthalmology which can guide an implant easily to an transplant place without causing any damage to the implant when the implant is inserted into an eyeball. [MEANS FOR SOLVING PROBLEMS] The injector for an eye used for inserting an implant into an eyeball comprises an outer tube, and an implant holding structure arranged in the outer tube to be slidable with respect to the outer tube. The implant holding structure has an implant holding portion which can be contained in the outer tube and forms a space for containing the implant between the implant holding portion and the inner surface of the outer tube when it is contained in the outer tube. The implant holding portion projects from the outer tube when the implant holding structure is advanced and the implant can be taken out from the outer tube.

Abstract: A device and method of use thereof for incrementally adjusting the size and/or shape of a particular body part is provided. The device comprises first and second layers each formed of a synthetic resin. The first layer is formed of a heat-shrinkable material having a low melting point while the second layer has a melting point much higher than the first layer. Upon being subjected to energy, the first layer will shrink or contract causing the second layer, and thus the overall device, to bend in the direction of contraction. In use, the device is inserted into the particular body part after which energy is applied to the device so as to cause the body to expand, move, reshape, etc. The invention is particularly useful for treatment of accommodative disorders of the eye by positioning one or more of the devices within the eye sclera or attached to the sclera around the limbus so that the sclera and ciliary body are expanded away from the crystalline lens upon being of the device.

Abstract: In surgery of the vitreous body in an eyeball of a human body, a burden on and time of a surgeon is suppressed from being spent, a burden on the eyeball of a patient is greatly reduced, and further, the possibility of a complication after the surgery is also lessened. A holding apparatus, which has eyelid opener portions for pulling and opening upper and lower eyelids, a lens ring for holding a surgical contact lens on the eyeball, and connecting portions for connecting the eyelid opener portions with the lens ring of the surgical contact lens so that the surgical contact lens is held on the eyeball, is set on the eyeball of the patient, which makes it unnecessary to stitch of the lens ring on the eyeball.

Abstract: A method of protecting tissue from trauma during a surgical procedure, the method comprising the step of coating at least a portion of the tissue with a viscoelastic composition comprising: a mixture of hyaluronic acid and/or salts thereof and hydroxypropyl methylcellulose, wherein the concentration of hyaluronic acid and/or salts thereof is a minimum of about 0.1% w/v and a maximum of about 6% w/v and the concentration of hydroxypropyl methylcellulose is a minimum of about 0.05% w/v and a maximum of about 5% w/v, based upon the total volume of the viscoelastic composition; tris[hydroxymethyl]aminomethane at a maximum of about 50 mM and a minimum of about 0.1 mM based upon the total weight of the viscoelastic composition; and a hexahydric alcohol.

Abstract: Apparatus for performing intraocular implant surgery, including surgical apparatus for performing intraocular implant surgery, an autorefraction device associated with the surgical apparatus, wherein the autorefraction device is configured to perform autorefraction on the aphakic eye to provide one or more aphakic refraction measurements, and a processor connected to the autorefraction device, wherein the processor is configured to process the aphakic refraction measurements and provide the user of the apparatus with information regarding the power of the intraocular lens.

Abstract: A shipping system for a medical device, such as implantable lens for an eye, is provided that may be reconfigured from a shipping mode into an injection mode without manually handling the contained lens or other device. Upon manufacture, a lens may be placed within the system assembly in the shipping configuration. While in the shipping configuration, the lens is kept in its desired shape and within a selected environment. Upon arrival at the destination, the user may attach fittings for injection of the device into a body. The process of changing from the shipping to the injection mode deforms the device into a shape suitable for injection. A new assembly for insertion of a medical device utilizing the shipping systems is also disclosed.

Abstract: This apparatus is a device for removal of cataracts from the eyes of patient. The apparatus includes a hand piece, with an irrigation water line, a vacuum line and a power line provided therein, are all connected with the hand piece. Within the hand piece the vacuum line is attached to a tube, identified as the horn, concentric with the outer shell of the hand piece. Through a hooks and slider joint, bayonet type or threaded joint in the front end, the horn connects with a surgical needle. At the front end of the irrigation tube it discharges water into a chamber, which irrigation water passes between the needle and an outer sleeve and into the anterior chamber of the eye. Ultrasonic waves transmitted to the horn are conveyed to the tip of the needle where the axial vibrations of the tip may be used to comminute cataract material.

Abstract: Apparatus for performing intraocular implant surgery, including surgical apparatus for performing intraocular implant surgery, an autorefraction device associated with the surgical apparatus, wherein the autorefraction device is configured to perform autorefraction on the aphakic eye to provide one or more aphakic refraction measurements, and a processor connected to the autorefraction device, wherein the processor is configured to process the aphakic refraction measurements and provide the user of the apparatus with information regarding the power of the intraocular lens.

Abstract: An injector for inserting an intraocular lens (IOL) into an eye, comprising: a first side wall and a second side wall which are movable relative to one another, each side wall including a void, the voids positioned opposite one another in a direction perpendicular to a longitudinal axis of the injector. The injector may be in a combination with the IOL, the IOL disposed on a portion of the injector. The IOL may be in an unstressed state. A first portion of a haptic of the IOL may extend into the void in the first side wall.

Abstract: A system for easily transferring an intraocular lens (IOL) from an inserter into a patient's eye. The system includes an inserter handpiece with a holding station for receiving or storing an IOL. The IOL may be pre-loaded within the holding station during manufacture, and the inserter handpiece coupled to a delivery tube so that the entire system is ready for use by a surgeon to implant an IOL. The IOL may have an optic and leading and trailing haptics coupled to the optic, and the holding station may be capable of manipulating the haptics as desired to facilitate transfer of the IOL through the delivery tube into the eye. For instance, the holding station may fold one or both of the haptics over the optic. Preferably, the holding station maintains the haptics in their folded positions during transfer of the IOL into the delivery tube. The holding station desirably maintains the IOL in a relaxed configuration during storage.

Abstract: A device and method of use thereof for incrementally adjusting the size and/or shape of a particular body part is provided. The device comprises first and second layers each formed of a synthetic resin. The first layer is formed of a heat-shrinkable material having a low melting point while the second layer has a melting point much higher than the first layer. Upon being subjected to energy, the first layer will shrink or contract causing the second layer, and thus the overall device, to bend in the direction of contraction. In use, the device is inserted into the particular body part after which energy is applied to the device so as to cause the body to expand, move, reshape, etc.

Abstract: An injector and method for injecting a dual optic AIOL into an eye wherein the AIOL is loaded into the injector in an initially loaded condition with the first and second optics in generally coaxial alignment. A lens moving element is provided and operable to move the first optic toward the proximal end of the main body whereupon the first optic becomes located proximally of the second optic. A stop may be provided to prevent the second optic from moving proximally with the first optic. Displacing the optics to a non-coaxial position reduces the cross-sectional area of the AIOL which allows the AIOL to non-destructively compress to the size of the opening of the injector tip which may be as small as about 2.8 mm or less, for example.