Abstract: A prosthetic capsular device configured to be inserted in an eye includes a housing structure and a ring structure. The housing structure includes a first side, a second side opposite the first side, a third side, a fourth side opposite the third side, a posterior side including a refractive surface, an anterior side opposite the posterior side, and a longitudinal axis. The first side, the second side, the third side, the fourth side, the posterior side, and the anterior side at least partially define a cavity configured to contain an intraocular device (e.g., an IOL). The anterior side includes an opening. The ring structure includes a ring structure portion extending radially outward from proximate one of an end of the first side and an end of the second side.

Abstract: A prosthetic capsular device configured to be inserted in an eye includes a housing structure and a ring structure. The housing structure includes a first side, a second side opposite the first side, a third side, a fourth side opposite the third side, a posterior side including a refractive surface, an anterior side opposite the posterior side, and a longitudinal axis. The first side, the second side, the third side, the fourth side, the posterior side, and the anterior side at least partially define a cavity configured to contain an intraocular device (e.g., an IOL). The anterior side includes an opening. The ring structure includes a ring structure portion extending radially outward from proximate one of an end of the first side and an end of the second side.

Abstract: A lens delivery system having a plunger rod with a sliding block reinforcing member. The sliding block rides on and along with the plunger rod and helps to reinforce the plunger rod against bending or buckling during use.

Abstract: A mitral valve prosthesis and methods for implanting the prosthesis transapically (i.e., through the apex of the heart), transatrially (i.e., through the left atrium of the heart), and transseptally (i.e., through the septum of the heart). The prosthesis generally includes a self-expanding frame and two or more support arms. A valve prosthesis is sutured to the self-expanding frame. Each support arm corresponds to a native mitral valve leaflet. At least one support arm immobilizes the native leaflets, and holds the native leaflets close to the main frame.

Abstract: A delivery system for percutaneously deploying a prosthetic heart valve. The system includes an inner shaft assembly, a delivery sheath capsule and a handle maintaining a first actuator and a second actuator. The capsule is configured to compressively retain the prosthetic heart valve over the inner shaft assembly. The first actuator is operated to proximally retract the delivery sheath capsule and expose the prosthetic heart valve relative to the capsule. The second actuator is operated to proximally retract the prosthetic heart valve by transmitting forces to the inner shaft assembly.

Abstract: A delivery device usable to deliver an inverting implant is provided that includes a positioning mechanism that automatically initiates the inversion process once a predetermined length of the implant has exited a delivery catheter. The positioning mechanism allows the implant to be safely and accurately deployed with reduced operator experience and in a greater variety of target locations.

Abstract: A dual poppet valve assembly for a pump assembly of an implantable penile prosthesis having a suction poppet engagable by a plurality of fingers allowing free travel of the poppet and to prevent vacuum lockup of the pump assembly. The suction poppet can also include an elongated shaft receivable within a corresponding bore of a cylinder poppet to prevent the suction poppet from becoming misaligned during the operation of the pump assembly.

Abstract: The present invention provides for a variety of fracture fixation options should a fracture occur after total hip arthroplasty or total knee arthroplasty, and provides associated methods and apparatus for application of provided fixation. The ability to pre-engineer fracture fixation contingent solutions into femoral or tibial components provides for a distinct clinical advantage in the planning and execution for periprosthetic fracture fixation. Said methods and apparatus include targeting devices which allow for intimate association of fixed angle locking screws in pre-drilled holes in an existing prosthetic, femoral nail, or other components including additional fixation components. Use of pre-engineered fracture fixation contingent solutions into femoral or tibial components provides for a distinct clinical advantage in the planning and execution for periprosthetic fracture fixation.

Abstract: Shoulder arthroplasty systems and configurations for components thereof are described. For example, implant systems for a total should arthroplasty (TSA), hemi shoulder arthroplasty, and reverse should arthroplasty (RSA) are described. In addition, exemplary configurations for baseplates, glenoid components, glenosphere components, humeral components, humeral head components, humerosocket components, connectors, and adaptors, are described.

Abstract: An articulating fusible support cage comprises a first support member having a first and second end and a second support member having a first and second end. A first end cap is pivotally connected to the first and second support members at the first ends. The first end cap supports a jackscrew for rotation. A second end cap is pivotally connected to the first and second support members at the second ends opposite the first ends. The second end cap has a threaded sleeve configured to engage a portion of the jackscrew. Rotation of the jackscrew into the threaded sleeve causes the first and second support members to extend outwardly from a collapsed condition to a deployed condition.

Abstract: A spinal cage with a wall extending in a longitudinal direction defining an interior space is disclosed. There is also provided a deployable element in movable relation to the spinal cage. In some embodiments, there is a rib, and the rotatable member is engaged at one end with the wall and at the other end with the rib. In some embodiments, the spinal cage is provided with holes for screws that can be directed at adjacent vertebrae for fixation. Such a spinal cage can be used with the spin-plate or with the screws. The screws and the spinal cage may have features that cooperate to prevent back-out of the screws.

Abstract: An adjustable spinal fusion intervertebral implant including upper and lower body portions each having proximal and distal surfaces at proximal and distal ends thereof. The implant can include a proximal wedge member disposed at the proximal ends of the respective ones of the upper and lower body portions, and a distal wedge member disposed at the distal ends of the respective ones of the upper and lower body portions. First and second linkages can connect the upper and lower body portions. Rotation of an actuator shaft can cause the distal and proximal wedge members to be drawn together such that longitudinal movement of the distal wedge member against the distal surfaces and the longitudinal movement of the proximal wedge member against the proximal surfaces causes separation of the upper and lower body portions.

Abstract: An implanting apparatus and an operating method thereof are provided. An implanting apparatus used for implanting an intervertebral cage into a location between two adjacent vertebral bodies, wherein the implanting apparatus comprises a sleeve and an extension member. The extension member has a rod and a coupling column, wherein the rod is screwed inside the sleeve, the coupling column is connected to one end of the rod and exposed outside the sleeve, and the axial direction of the coupling column is substantially perpendicular to that of the rod. When one end of the coupling column is disposed on an inner arc surface of a connecting portion of the intervertebral cage and the rod is rotated with respect to the sleeve, the distance between the coupling column and the sleeve is decreased so as to clamp the connecting portion of the intervertebral cage between the coupling column and the sleeve.

Abstract: Articles made of a porous material having a fibrillar microstructure of bent fibrils and provided with a fracturable coating whereby the physical size of the article may be changed by the application of force to the article in a direction substantially parallel to a direction of orientation of the fibrils. The application of a tensile force to such an article in a direction substantially parallel to orientation of the bent fibrils results in fracturing of the fracturable material and straightening of the bent fibrils. Methods of making such articles are also described. The articles may include implantable articles such as vascular grafts and stent-grafts; such devices may, for example, be forcibly increased in diameter or in length wherein the force results in fracturing of the coating. One such coated material is porous expanded polytetrafluoroethylene provided with a coating of fluorinated ethylene propylene.

Abstract: An endovascular stent graft delivery device has portion to remain outside a patient in use and a proximal portion to be introduced into a patient. The proximal portion has a dilator at the proximal end and a length extending module is fastened to the dilator and extends proximally. The length extending module has a proximal end which in use extends out of the patient. The dilator has a dilator marker and the length extending module has a first and second marker at the distal and proximal ends of the length extending module. The first marker and the second marker are at the same relative circumferential position on the length extending module so that the rotational position of the elongate body within the patient can be determined.

Abstract: A stent delivery system is configured so that its outer diameter can be reduced when the balloon is folded and the stent is mounted on the folded balloon. The stent delivery system includes a balloon which is expandable by injection of fluid inside the balloon, and is folded in the form of stacked layers around an outer circumference of an elongated inner tube. The stent delivery system also includes a stent having a plurality of annular parts, each formed with a wire in an annular shape and arranged in the direction of the axis of the stent, and a plurality of connecting parts connecting the neighboring annular parts. All the connecting parts are arranged on the outer circumference of the balloon in a manner that each of the connecting parts is positioned on a minimum-layered portion having the smallest number of stacked layers.

Abstract: An ankle support for wearing over a person's lower leg and foot is disclosed. The ankle support includes a yoke made of a semi-rigid, flexible material. The yoke includes a shin portion and a stirrup portion. A removable cap that is adapted for extending over the stirrup portion of the yoke is used with the ankle support. The removable cap includes a groove for engaging the stirrup portion of the yoke. Additionally, a separate shin section cover that is adapted for extending over the shin portion of the yoke and include a groove that will accept a mating portion of the yoke is also provided. The shin section cover can be varied independently of the removable cap.

Abstract: An orthotic brace and brace hinge where the brace comprises two hinge elements operably connected and at least one hinge element having a magnetic field that provides a magnetic force urging one of the hinge elements in a pre-determined direction. Embodiments of the present invention generally utilize magnetic forces to stabilize, influence and/or maintain adjacent joint portions in pre-determined desired relationships and for constraining motion and/or rotation of the joint portions. Through the use of the repelling and attracting forces of magnets, mechanical forces in the brace and brace hinge can be replaced or supplemented to reduce the force put on joint bones, to influence the bones so that the joint is biased into certain positions or to apply different forces through different points of joint flexion. Embodiments of braces with magnetic fields on other brace elements are also disclosed.

Abstract: A spinal orthosis is provided that includes a cervical section, a lumbar section, a thoracic section and a tensioner. The cervical section has one or more pads configured for placement at a clavicle of a wearer. The lumbar section is connected to the cervical section and has an abdominal Para-umbilical buttress configured for an anterior region of a lumbar spine. The buttress is further configured to provide compression and gripping of the spine. The lumbar section includes one or more digits with a gripping portion at around ribs and/or iliac crest of the wearer. The thoracic section is connected to the cervical section. The tensioner connects the lumbar section to the thoracic section.

Abstract: An apparatus and method are provided for positioning a patient on a surgical platform. The apparatus includes an elongated flexible web and a plurality of extension straps for connecting the apparatus to the surgical platform. Each extension strap includes a connector configured for connecting the apparatus to the platform. Adjustment mechanisms allow the extension straps to be adjusted to vary the tension in the web. The medical professional selects the desired position and orientation of the patient on the surgical platform and manipulates the patient into the desired position and orientation. A retention device is connected to a surgical platform and placed over the patient at the appropriate portion of the patient. A second end of the retention device is connected to a second side of the surgical platform. The retention device is then adjusted to increase the tension in the retention device.

Abstract: An ostomy bag with a filter construction is provided. The filter construction includes a deodorising element and an extension element. The extension element may function to provide buoyancy means so that a gas-inlet portion at the extension element is kept on top of the output or pushed away by the output. The extension element may also be attached to the ostomy bag at a distance from the deodorising element so as to provide a controlled flow path for the gas-flow.

Abstract: An intravenous heat exchange catheter and/or an external cooling pad/bladder can be used to maintain hypothermia in, e.g., a cardiac arrest patient, but to accelerate the cooling process the patient first can be infused with cold saline before the opportunity arises to connect the catheter or pad to the patient.

Abstract: Passive prosthetic devices for focally cooling a brain and methods for inhibiting seizures are disclosed. The prosthetic devices replace a thermally insulating bone flap with a thermally conductive insert having an inner surface that contacts the relatively warm meninges or brain and an outer surface that contacts the relatively cool scalp. In an embodiment, the prosthesis is unitary; in another, a biocompatible casing is filled with a highly conductive core; in another, a filled polymer block is attached to a plate; and in another, the bone flap is filled with a conductive polymer. In one embodiment, a filled polymer containing elements that exhibit the magnetocaloric effect provide heat transfer that can be enhanced by application of a suitable magnetic field. Focal cooling as low as 1.2° C. has been found effective at inhibiting seizures.

Abstract: A delivery device that allows for the sustained release of an agent, particularly useful for the sustained release of a therapeutic agent to limited access regions, such as the posterior chamber of the eye and inner ear. The delivery device is minimally invasive, refillable and may be easily fixed to the treatment area. The delivery device includes a hollow body with an inlet port at its proximal end for insertion of the agent, a reservoir for holding the agent and a delivery mechanism for the sustained delivery of the agent from the reservoir to the patient.

Abstract: Vitrectomy probes and system related thereto are disclosed herein. The disclosure describes vitrectomy probes having an adjustable cutting port size. The cutting port size may be adjusted by altering a position of a stroke limiter via a stepper motor. Various example features are described for adjusting the size of the cutting port.

Abstract: A sleep shield apparatus that can provide privacy, peacefulness, and protection in a public environment such as an airplane, airport, bus, or train is provided.

Abstract: A method of treating tinnitus comprising measuring a patient's hearing, determining the patient's hearing loss and the patient's tinnitus frequency using the measurements of the patient's hearing, programming a clinical controller with the measurements of the patient's hearing, selecting a plurality of therapeutic tones, where the therapeutic tones are selected to be at least a half-octave above or below of the patient's tinnitus frequency, setting an appropriate volume for each of the plurality of tones, repetitively playing each of the plurality of therapeutic tones, and pairing a vagus nerve stimulation pulse train with each playing of a therapeutic tone, thereby reducing the patient's perception of tinnitus.

Abstract: Embodiments of the disclosure include methods and devices for folding the earmuffs of a headset via at least two different axes of rotation. The headset may comprise a headband and two earmuffs, wherein the earmuffs are connected to the headband, and wherein the headband comprises a plurality of rotational axes, about which the earmuffs may be rotated in one or more directions. The movement of the earmuffs may allow for comfortable wearing of the earmuffs in different positions, such as around a wearer's neck, and may allow for compact carrying or storage of the headset. The headset and earmuffs may be designed to be used as hearing protection, wherein the earmuffs may be larger and comprise special material, and wherein the earmuffs may comply with regulations for hearing protection devices.

Abstract: A method of manufacturing a tampon includes transporting a web of material in a machine direction. The web of material has a base web and an absorbent web. The absorbent web has a free end and a bonded end wherein the bonded end is bonded to the base web. The free end of the absorbent web is moved in spaced relationship with the base web. The base web is bonded to a substrate.

Abstract: A disposable absorbent article including a chassis. The chassis includes a front region having two opposing longitudinal edges, a back region having two opposing longitudinal edges, and a crotch region having two longitudinal edges. The crotch region is disposed between said front and back regions, and at least two side panels extend outwardly from the two opposing longitudinal edges of one or both of the front or back regions. The side panels may interconnect the front and the back regions to form a waist opening and a pair of leg openings. The article exhibits a pre-application side panel length, Li, and a post-application side panel length, Lf, such that Li is less than Lf. The article may also include a plurality of graphics.

Abstract: An absorbent article may comprise a first zone comprising graphics and a second zone comprising graphics, wherein the first and second zones have different elastic properties. Further, the absorbent article may comprise a first absorbent article component and a second absorbent article component having substantially different elastic properties, wherein the first absorbent article component comprises an elastomer. Additionally, the absorbent article may comprise a third absorbent article component overlapping the first and second absorbent article components, wherein the third absorbent article component comprises graphics on at least the portions which overlap the first and second absorbent article components.

Abstract: An absorbent article, e.g. a diaper, having a topsheet, a backsheet, and an absorbent core disposed between them, the core having absorbent material provided in 3 regions of the core in certain amounts. The backsheet has a certain basis weight and is provided with a printed surface area. The topsheet has a minimum opacity.

Abstract: By programming position parameters corresponding to user support surfaces of a power driven wheelchair, movement of the user support surfaces is automated. The user support surfaces can be positioned individually, as part of a sequence or as part of a series of sequences. Accordingly, with little effort, a user can position the user support surfaces of the wheelchair to a predefined position.

Abstract: The invention relates to a bed for providing support in sitting up to a person lying thereon, comprising an approximately rectangular frame, which comprises at least two frame parts, which are separated from each other in the longitudinal direction and are connected to each other in an articulated manner and are completed to form a planar element by flexible slats, woven wire fabric, or the like and can be swiveled about a transverse axis oriented transversely to the respective frame part from the horizontal to an inclined position, wherein at least one sit-up area lies on at least one frame part, said sit-up area being integrated into the surface of the frame part in the deactivated state, the outward-facing edge of said sit-up area extending approximately to the border of the frame and the inward-facing edge of said sit-up area being at a distance from the center line of the frame extending in the longitudinal direction, wherein said sit-up area can be swiveled about a sit-up axis extending parallel or at a

Abstract: Hardware for a casket comprises a clevis having a pair of side walls, a back wall adapted to be attached to the casket shell wall, a pair of tabs each of which extends laterally outwardly from a respective one of the side walls and each of which is spaced forwardly from the rear wall, an arm pivoted at an upper end to the clevis, and a decorative ear having a downwardly facing recess in a lower edge thereof and a pair of tapered resilient arms each of which is located on a respective side of the recess, each resilient arm having a laterally inwardly projecting tab on a lower free end thereof, each resilient arm becoming progressively thicker from the free end toward a base thereof as measured in a direction generally normal to the casket shell wall.

Abstract: The present teachings provide for an exercise device for exercising a joint and a limb. The device includes an actuator, a foot plate, a foot plate load cell, and a restrictor. The actuation member is rotatable about a rotation axis. The actuation member includes a first portion and a second portion that is movable in a direction perpendicular to the rotation axis. The foot plate is at a distal end of the second portion of the actuation member. The foot plate load cell is mounted to the foot plate and is configured to measure force exerted on the foot plate. The restrictor is configured to restrict movement of the second portion of the actuation member and the foot plate at the distal end thereof in the direction perpendicular to the rotation axis unless force exerted on the foot plate exceeds a predetermined force.

Abstract: A method for mobilizing a hip joint capsule of a patient using a resilient bolster. In accordance with the method, the patient assumes a lateral position, with the hip capsule to be treated superior. The resilient bolster is placed between the patient's legs as proximal to the patient's crotch. A force is applied to patient's superior leg to move it downwardly from a resting position. During downward movement of the patient's superior leg, the bolster functions as a fulcrum and the patient's superior femur functions as a lever arm to create a first class lever that partially distracts the femoral head from the acetabulum. After application of the force, the resiliency of the bolster causes the patient's superior leg to return to the resting position. The movements may be repeated, and the degree of hip flexion and rotation may be varied to affect different regions of the hip capsule.

Abstract: Systems and methods related to the field of cardiac resuscitation, and in particular to devices for assisting rescuers in performing cardio-pulmonary resuscitation (CPR) are described herein. A method for managing cardiopulmonary resuscitation (CPR) treatment to a person in need of emergency assistance includes monitoring, with an electronic medical device, a parameter that indicates a quality level of a CPR component being provided to the person by a user; determining, with the electronic medical device, that the parameter indicates that the quality level of CPR being provided is inadequate; and providing, to one or more rescuers of the person, an audible, visual, or tactile indication that a different person should perform the CPR component.

Abstract: Medicant mixing/administration systems are provided that can include: a medicant vial; a syringe assembly comprising a barrel and a piston; a protective material supporting the syringe assembly and medicant vial; and a member within the system, the member separating the piston of the syringe assembly from the medicant vial. Systems are provided that can include: a syringe assembly comprising a barrel and a piston; having a forward end and an opposing back end; a protective material supporting the syringe assembly; and a needle housing coupled to the protective material. Medicant mixing/administration methods are also provided that can include, within a package, sufficiently clearing a restraining member from between a medicant vial and syringe plunger to pierce the medicant vial with a piercing structure coupled to the syringe plunger, the piercing providing medicant from the vial to the syringe assembly.

Abstract: A reconstitution device having an opening surrounded by a neck, and a cap including a first end, a second end, and an inner bore having a central aperture. A stopper is positioned in the opening of the neck and includes a portion capable of being perforated. A plunger is located at the second end of the cap, is configured to slide along the inner bore of the cap, and includes a shaft extending downwardly in a direction towards the stopper and having a pointed end for piercing the stopper. A locking mechanism is located in the cap and includes an aperture. The locking mechanism is configured such that when the plunger is pushed downwardly the shaft is allowed to pass through the aperture, but when the plunger is pulled upwardly the second aperture changes shape such that the shaft cannot freely pass through the aperture.

Abstract: A self-cure, dual-cure or tri-cure polymerizable dental composition is provided with at least one functional chemical. The dental composition is divided into a three-part composition to avoid stability issues caused by degradation and/or loss of function of one component in the extended presence of another component, and the three parts are packaged in a tri-barrel syringe or cartridge delivery system to avoid premature chemical interaction between the functional chemical, redox initiator and/or acid/base.

Abstract: The invention relates to a dental restorative material on the basis of at least one compound of one of the Formulae The invention also relates to the use of the dental restorative materials according to the invention for preparing dental composites, preferably composite blanks, which are suitable in particular for mechanical processing by means of computer-aided processing techniques such as milling and grinding processes, and which are suitable above all for preparing dental restoration materials such as inlays, onlays, crowns, bridges or veneering materials.

Abstract: A micro electromechanical ink jet printing system that has a cartridge having a body that defines a core, and a die that contains one or more nozzles. There is a treatment composition contained within the cartridge core. The system further includes a CPU that is programmable and can control the application of the treatment composition from within the cartridge core, through the one or more nozzles to human skin. Typically, the treatment composition will contain a skin treatment ingredient selected from the group consisting of particles, vitamins, yeast and yeast extracts, skin care actives, dyes, colorants and mixtures thereof. There may optionally be provided a bladder or foam block disposed within the cartridge core for suspending and regulating the flow of the treatment composition. The systems of this invention may include an applicator having an applicator head having one or more applicator nozzles which may be in a array.

Abstract: Disclosed and claimed herein are a composition and a kit for coloring keratin fibers, and processes of their use. The composition includes a catechol-based color precursor.

Abstract: Disclosed herein are compositions comprising a fluoride ion source, a poly(propylene oxide)/poly(ethylene oxide) copolymer, and optionally a sparingly soluble acid; and methods of using and of making the same.

Abstract: Provided is a gelling agent containing N-acyl acidic amino acid dialkylamide having a DL form ratio (D form/L form (weight/weight)) of 5/95-20/80 or 80/20-95/5, and using the gelling agent, a gel composition, particularly a rod-like gel composition, superior in transparency and strength, and superior in compatibility and spreadability when applied to the skin, hair and the like is provided.

Abstract: A skin cleansing composition, comprising (A) an alkyl ether carboxylic acid or a salt thereof represented by formula (1): wherein, R1 represents an alkyl group having 8 to 18 carbon atoms, n represents a number of from 0 to 20, and M represents a hydrogen atom, alkali metal, alkaline earth metal, ammonium, or organic ammonium, wherein, R1 has an average carbon number of from 10.8 to 12.8 and the average value of n is from 2.5 to 3.4, and wherein, the alkyl ether carboxylic acid or a salt thereof contains a component in which n=0 in an amount of from 9.

Abstract: A subject-matter of the invention is a method for dyeing and/or lightening keratinous fibres, such as the hair, employing i) at least one direct dye having a disulphide, thiol or protected thiol functional group and ii) at least one thickening organic polymer, iii) at least one (poly)ethoxylated fatty alcohol and/or one nonionic surfactant, iv) at least one alkaline agent and v) at least one reducing agent. Another subject-matter of the invention is a composition comprising the ingredients i) to v), the use of the combination of i), ii), iii), iv) and v) for dyeing and/or lightening keratinous fibres and a multicompartment kit comprising the ingredients i) to v). The dyeing method and the composition according to the invention make it possible in particular to obtain a lasting coloration on keratinous fibres which is intense, chromatic and/or homogeneous, with or without the use of an oxidizing agent.

Abstract: A composition is disclosed that includes pure silk fibroin-based protein fragments that are substantially devoid of sericin, wherein the composition has an average weight average molecular weight ranging from about 17 kDa to about 38 kDa, wherein the composition has a polydispersity of between about 1.5 and about 3.0, wherein the composition is substantially homogeneous, wherein the composition between 0 ppm to about 500 ppm of inorganic residuals, and wherein the composition includes between 0 ppm to about 500 ppm of organic residuals.

Abstract: A composition is disclosed that includes pure silk fibroin-based protein fragments that are substantially devoid of sericin, wherein the composition has an average weight average molecular weight ranging from about 17 kDa to about 38 kDa, wherein the composition has a polydispersity of between about 1.5 and about 3.0, wherein the composition is substantially homogeneous, wherein the composition between 0 ppm to about 500 ppm of inorganic residuals, and wherein the composition includes between 0 ppm to about 500 ppm of organic residuals.