Abstract: System, ophthalmic lens, and method for extending depth of focus includes an optic having a clear aperture disposed about a central axis. The optic includes a first surface and an opposing second surface. The first and second surfaces are configured to introduce an asymmetric aberration to the eye while maintaining the in-focus visual acuity.

Abstract: There is provided an implant which is utilized in the treatment of corneal defects and conditions, such as for example Keratoconus. An intracorneal implant is provided having a first and second curved segment, which form a ring-like device. The first and second curved segments of the ring-like device are detached. The ring-like device has an inner diameter in the range of 4.95 mm to 5.25 mm and an outer diameter in the range of 6.8 mm to 7.1 mm. The first and second curved segments are symmetrical in cross section and are comprised of a transparent material.

Abstract: An intraocular lens includes a lens capsule expanding device and an optical portion. The lens capsule expanding device includes a front supporting portion to make contact with an inner surface of an anterior capsule. A rear supporting portion provided on a rear side of the front supporting portion makes contact with an inner surface of a posterior capsule while facing the front supporting portion. A connecting portion connects the front supporting portion and the rear supporting portion so as to have biasing force in a direction of separating the front supporting portion and the rear supporting portion from each other. Due to the biasing force, the front supporting portion presses the inner surface of the anterior capsule and the rear supporting portion presses the inner surface of the posterior capsule. The optical portion changes the curvature of a central portion according to movement of the connecting portion.

Abstract: An implant system for implantation at a joint, the implant system including an implant device which includes a body portion having first and second ends, and a first elongate member, extending from the first or second end of the body portion. The implant system also includes a corresponding fixation device for securing the first elongate member to a subject, and the fixation device includes at least one latching element, the first elongate member includes at least one cooperating element, the at least one cooperating element being capable of cooperating with the at least one latching element of the fixation device in use.

Abstract: A prosthesis for primary artrodhesis can be used for artroplasty and a prosthesis for artroplasty comprises members for artrodhesis. The prosthesis (1b) for primary artrodhesis comprises a locking member (33b) with an attachment portion (16b) which is insertable into a hole (8b) in a first attachment member (4b) of the prosthesis for location of the locking member therein, and a lockable member (34b) integral with a second attachment member (5b) of the prosthesis. The lockable member (34b) is configured for adjustable setting thereof relative to the locking member (33b) and for fixation thereof, in set position, to the locking member. Alternatively, the lockable member comprises an attachment portion which is insertable into a hole in the second attachment member for location of the lockable member therein.

Abstract: An accommodating IOL includes a flexible optic membrane, a flexible skirt extending from an outer periphery of the flexible optic membrane and defining an outer periphery of the accommodating IOL, and a capsular contact ring configured to be positioned anterior to the flexible optic membrane and having a diameter less than a diameter at the outer periphery of the accommodating IOL. The accommodating IOL further includes a plurality of strut assemblies connecting the capsular contact ring and flexible skirt. When the capsular bag transitions from an accommodative state to a disaccomadative state, the capsular bag exerts a force on the capsular contact ring, at least a portion of that force being transferred to the flexible skirt by the plurality of strut assemblies. The transferred force causes a flattening of the flexible optic membrane in a manner that reduces the optical power of the accommodating IOL.

Abstract: An orthopedic surgical instrument system for use in preparing a patient's bone is disclosed. The surgical instrument includes a cutting guide block configured to be secured to a surgically-prepared surface of the patient's bone, and a cutting tool to be used in conjunction with the cutting guide block to resect a section of the patient's bone. A method of performing an orthopedic surgery is also disclosed.

Abstract: A prosthesis for primary artrodhesis can be used for artroplasty and a prosthesis for artroplasty comprises members for artrodhesis. The prosthesis (1b) for primary artrodhesis comprises a locking member (33b) with an attachment portion (16b) which is insertable into a hole (8b) in a first attachment member (4b) of the prosthesis for location of the locking member therein, and a lockable member (34b) integral with a second attachment member (5b) of the prosthesis. The lockable member (34b) is configured for adjustable setting thereof relative to the locking member (33b) and for fixation thereof, in set position, to the locking member. Alternatively, the lockable member comprises an attachment portion which is insertable into a hole in the second attachment member for location of the lockable member therein.

Abstract: A prosthetic capsular device configured to be inserted in a natural capsular bag of an eye after removal of a lens includes a housing structure capable of containing an intraocular device. The housing structure includes a posterior side, an anterior side opposite the posterior side, lateral sides extending between the posterior side and the anterior side, and a cavity at least partially defined by the posterior side, the anterior side, and the lateral sides. The posterior side includes a refractive surface and an opening radially outward of the refractive surface. The anterior side includes an aperture capable of allowing at least one of insertion, removal, and replacement of an intraocular device. The cavity is capable of containing an intraocular device.

Abstract: An intraocular lens includes a lens capsule expanding device and an optical portion. A front supporting portion makes contact with an inner surface of an anterior capsule. A rear supporting portion makes contact with an inner surface of a posterior capsule while facing the front supporting portion. A connecting portion connects the front supporting portion and the rear supporting portion so as to have a biasing force to separate the front supporting portion and the rear supporting portion. Due to the biasing force, the front supporting portion presses the inner surface of the anterior capsule and the rear supporting portion presses the inner surface of the posterior capsule. The optical portion changes the curvature of a central portion according to movement of the connecting portion that moves the front supporting portion and the rear supporting portion closer to or away from each other with movement of the lens capsule.

Abstract: A two-piece socket for a ball-and-socket arrangement, including a base and a cap. The socket includes a leg on one of the cap or base of the socket and a receiving groove on the other of the cap or base of the socket, wherein there is at least one opening in the leg which lines up with a corresponding opening in the groove for a fastener to extend through these openings to releasably secure the cap to the base of the socket. The orientation of the fastener is such that the fastener is under shear loading when the cap is pulled apart from the base.

Abstract: The novel design of the one piece self-locking scleral buckle eliminates the need for a separate tire, band and sleeve by incorporating the band with the tire and making the device self-locking so the sleeve is no longer necessary. As one piece of silicone replaces the need for three separate pieces of silicone scleral buckling surgery is simplified thus making the procedure faster, safer and more efficient. The novel design of the scleral buckle placement instrument allows the surgeon to more firmly grasp the silicone material making the procedure faster and more efficient.

Abstract: Methods for altering the natural history of degenerative disc disease and osteoarthritis of the spine are proposed. The methods focus on the prevention, or delayed onset or progression of, subchondral defects such as bone marrow edema or bone marrow lesion, and subchondral treatment to prevent the progression of osteoarthritis or degenerative disc disease in the spine and thereby treat pain.

Abstract: The present disclosure provides devices and methods relating to surgical breast procedures. The devices can include a holder and backing to assist in positioning a biological material adjacent to a tissue expander or implant.

Abstract: A method for treating arthritis of a joint includes identifying a bone lesion in a bone adjacent to the joint; and implanting in the bone a reinforcing member in or adjacent to the bone lesion. A kit for conducting the method includes: (a) at least one reinforcing member having a proximal face adapted to face the joint, a distal face adapted to face away from the joint, and a wedge-shaped edge adapted to pierce bone, wherein the at least one reinforcing member is planar and sterile; and (b) a container adapted to maintain the at least one reinforcing member sterile. Another kit includes: (a) a sterile fluid; (b) a syringe for injecting the fluid into a bone; (c) a curing agent adapted to cure the fluid to polymerize and/or cross-link; and (d) a container adapted to maintain the sterility of contents of the container.

Abstract: A rotatable arm is provided which provides an ability to rotate a working end of an instrument such as a surgical retractor. Rotation of a key hub transfers torque to a drive hub which causes an extension or retraction of a lead screw along a center axis of the rotating arm. The extension or retraction forces a drive pin to bear against sides of helical slots of a driven tip, producing a rotation of the driven tip along a pitch line of the helical slots. The driven tip is connected to the working end such that the two rotate together. The rotatable arm has a low profile, a non-reversible torque transmission, and may be hermetically sealed.

Abstract: A method for adjusting a light adjustable lens in an optical system includes providing a light adjustable lens in an optical system; providing an ultraviolet light source to generate an ultraviolet light; and irradiating the generated ultraviolet light with a light delivery system onto the light adjustable lens with a center wavelength and with a spatial irradiance profile to change a dioptric power of the light adjustable lens by changing a refraction of the light adjustable lens in a refraction-change zone, thereby causing a wavefront sag, defined as half of a product of the change of the dioptric power and the square of a radius of the refraction-change zone, to be within 10% of its maximum over an ultraviolet spectrum.

Abstract: A stent/graft assembly includes a tubular graft connected in substantially end-to-end relationship with a generally tubular stent. Free ends of the stent and graft extend in opposite directions from the end-to-end connection during a pre-deployment orientation of the assembly. However, the graft is inverted during deployment so that free ends of the graft and the stent extend in substantially the same direction from the end-to-end connection in a post-deployment orientation. Thus, at least a portion of the stent is disposed within at least a portion of the graft in a post-deployment orientation of the assembly.

Abstract: The invention provides an intra ocular lens assembly comprising an intra ocular lens structure (IOL) for placement in the capsular bag and securing the IOL in an opening in an anterior part of a capsular bag, with an anterior capsular bag flap surrounding said opening, and a secondary intraocular lens (S-IOL) comprising fixing parts for attaching said S-IOL to said IOL.

Abstract: An orthopedic knee prosthesis includes a tibial bearing and a femoral component configured to articulate with the tibial bearing. The femoral component includes a posterior cam configured to contact a spine of the tibial bearing and a condyle surface curved in the sagittal plane. The radius of curvature of the condyle surface decreases gradually between early-flexion and mid-flexion. Additionally, in some embodiments, the radius of curvature of the condyle surface may be increased during mid-flexion.