Abstract: Intraocular lenses include a lens body sized and adapted for placement in a mammalian eye and having a plurality of different optical powers, and a movement assembly joined to the lens body and adapted to cooperate with the mammalian eye to effect accommodating movement of the lens body in the eye. Such intraocular lenses provide enhanced accommodation relative to the accommodation attainable using a single optical power IOL adapted for accommodating movement.

Abstract: The length of dwelling of a voice prosthesis in the fistula of a patient is extended by supporting the soft hollow body of the prosthesis with an elongated, rigid cartridge and mounting the flapper valve by means of a tab which extends through a slot in the flange of the cartridge. An enlarged cavity in the flange or the body communicates with the slot and receives the leading portion of the tab. The cavity is filled with adhesive to secure the valve to the cartridge.

Abstract: The length of dwelling of a voice prosthesis in the fistula of a patient is extended by supporting the soft hollow body of the prosthesis with an elongated, rigid cartridge and mounting the flapper valve by means of a tab which extends through a slot in the flange of the cartridge. An enlarged cavity in the flange or the body communicates with the slot and receives the leading portion of the tab. The cavity is filled with adhesive to secure the valve to the cartridge.

Abstract: A subcutaneously implantable medication infusion device includes a variable capacity reservoir for receiving and storing fluid medication for delivery to a catheter which directs the medication to a specific infusion location in the body. A control assembly is interposed between the reservoir and the catheter to facilitate and control the transfer of the medication from the reservoir to the catheter in a safe and efficient manner. The control assembly includes a self-recharging pump and a normally closed valve, both of which are manually actuable by percutaneous pressure when subcutaneously implanted, and defines a portion of a fluid flow conduit between the reservoir and the catheter. The control assembly is constructed to permit the infusion of a measured bolus of medication on demand through manual percutaneous manipulation of the control assembly.

Abstract: A ventriculostomy reservoir includes a rigid base and an elastomeric cap which is positioned over the base to enclose a reservoir well. A rigid cap insert is captured by the lower portion of the cap and is positioned for engagement with the base. The cap insert and the base are configured so that the cap may be snap-fit onto the base in a manner forming a fluid-tight seal therebetween. In one form of the invention, the cap insert includes a cylindrical portion which extends downwardly from a flange-like portion captured within the cap, to fit within an upwardly extending wall portion of the base. The cylindrical portion includes an encircling protrusion on an exterior surface thereof which engages and fits within an encircling detent provided on the interior surface of the wall portion to snap-fit the cap to the base. In a second embodiment of the invention the cap insert exteriorly surrounds an upper end of the base, and a similar protrusion and detent arrangement is utilized to snap-fit the cap to the base.

Abstract: A surgically implantable shunt system, including a flow control valve and an antechamber, is provided for controlling the release of entrapped body fluids. The flow control valve includes a pair of molded plastic bases situated, respectively, adjacent to an inlet and an outlet of the valve, which bases are situated within a flexible encasement. Each base includes an outer housing, a valve membrane carrier positioned within the housing, and a flow control member. The flow control members each include a rigid nail-like central support and a separate flexible resilient membrane positioned on the central support. A first flow control member is capable of selectively occluding the valve inlet, but is normally spaced from its base to permit free fluid flow through the inlet. The second flow control member is generally arch-shaped and resiliently biased to contact its respective base generally along the outer edge of the membrane in a manner permitting only controlled one-way flow through the valve.

Abstract: A subcutaneously implantable siphon control device is provided for use in a physiological shunt system including a proximal catheter, a flow control valve and a distal catheter. The siphon control device limits fluid flow through the shunt system due to the siphoning effect of hydrostatic pressure created by the elevation of the proximal catheter inlet with respect to the distal catheter outlet. The siphon control device includes, generally, a base having an inlet typically placed in fluid communication with an outlet of the flow control valve, and an outlet typically placed in fluid communication with the distal catheter, and a housing for the base which, in connection with the base, defines a fluid flow pathway between the inlet and the outlet. The base provides a wall having substantially parallel upper and lower seating surfaces, which separates the inlet from the outlet.

Abstract: A wound drainage reservoir which is a container having a resilient sidewall that defines a chamber within the container and wherein an opening extends through the sidewall. A helmet extends through the opening, which helmet has an extending lip that engages a portion of the sidewall of the container which surrounds the opening. A collar encircles and is bonded to the helmet for sealing such a portion of the sidewall between the lip of the helmet and the collar. A first inlet is on the helmet to provide a first fluid-flow conduit to the chamber. A second inlet is on the helmet to provide a second fluid-flow conduit to the chamber. A drainage outlet is on the helmet to provide a fluid-flow conduit from the chamber. A plurality of ribs extend laterally along the sidewall.