Abstract: A hip implant having two distinct bodies, a neck body and a bone fixation body. The neck body is formed from a solid metal and has an interface for connecting to a femoral ball. The bone fixation body has an elongated shape and is formed as a porous structure that is inserted into an intramedullary canal of a patient.

Abstract: Implant apparatus and methods directed toward treating conditions involving the knee joint are disclosed. Full range of motion of the knee joint and tissue integrity are maintained in treatment approaches. In one particular approach, osteoarthritis of the knee joint is addressed by unloading one or more of the lateral and medial compartments.

Abstract: An orthopaedic knee prosthesis includes a femoral component which exhibits enhanced articular features, minimizes removal of healthy bone stock from the distal femur, and minimizes the impact of the prosthesis on adjacent soft tissues of the knee.

Abstract: An orthopaedic knee prosthesis is provided including a tibial baseplate component having a distal, bone-contacting surface with one or more fixation structures extending distally therefrom, in which the fixation structures are asymmetrically arranged within the baseplate periphery.

Abstract: A total ankle replacement system, novel surgical method for total ankle replacement, and novel surgical tools for performing the surgical method are described. The total ankle replacement system includes the calcaneus in fixation of a lower prosthesis body, thereby significantly increasing the amount of bone available for fixation of the lower prosthesis body and allowing the lower prosthesis body to be anchored with screws. The total ankle replacement system further includes a long tibial stem which can also be anchored into the tibia with, for example, screws, nails, anchors, or some other means of attachment. The novel surgical arthroscopic method allows introduction of ankle prostheses into the ankle joint through an exposure in the tibial tubercle. Various novel surgical instruments, such as a telescoping articulating reamer and a talo-calcaneal jig, which facilitate the novel surgical method, are also described.

Abstract: The invention relates to an implant device, comprising an actuating instrument (110) and a height-adjustable implant (10) having a substantially U-shaped inner basket (11) and a U-shaped outer basket (60), wherein the inner basket (11) of the implant (10) is embraced by the outer basket (60) and telescopically guided, and the inner basket (11) and outer basket (60) are equally aligned, and wherein the limb (12, 13) of the inner basket (11) and the limb (61, 62) of the outer basket (60) are aligned so that a substantially continuous lateral opening (80) results, and the inner (11) and outer (60) baskets can be fixed with respect to each other in a predetermined end position, and wherein vertebral support surfaces are provided on the end faces (18, 63) of the baskets (11, 60), wherein the actuating instrument (110) has a fixation rod (111) and an expansion mechanism with sliding elements (122), and the inner basket (11) and fixation rod (111) have corresponding elements (26, 112), by means of which a detachable

Abstract: Systems for interbody fusion of adjacent bone portions may include an expanding implant and related instruments. An expanding implant may be formed as a linkage which is movable between a compact configuration and an expanded configuration. A shaft of the implant may increase and decrease in length to move between the compact and expanded configurations, and an implant width perpendicular to the length may be increased in the expanded configuration. The implant width may increase more in a first direction than a second direction opposite the first direction. An inserter instrument may releasably grasp the spacer and transform the implant between the compact and expanded configurations.

Abstract: The invention relates to an intervertebral disc prosthesis for the total replacement of the intervertebral disc within the lumbar and cervical spine. For a two part as well as for a three part intervertebral disc prosthesis, according to the invention, in accordance to the design of the edges of the sliding partners, there are aspects for at least one of the sliding partners, in which there is an wavelike design of the edge, as the respectively different high edge regions preferably fluently merge.

Abstract: A hybrid mechanical device comprising rigid-body joints, such as rotational and planar joints, and one or more continuum joints that operate based on constitutive properties of materials, such as, for example, flexure, extension and compression. Embodiments include a tripartite nucleus comprising a cap, core, and sled. The cap is rotatably connected to a first end plate and the sled is rotationally and translationally connected to a second end plate. The joint surfaces between the nucleus and end plates of the device provide up to six degrees of freedom. The constitutive properties of the core can further provide a “continuum” joint to complete the hybrid mechanical motion producing structure. In certain embodiments, the cap, core and sled comprise the same or substantially the same material. But, in other embodiments, the cap, core and sled comprise different materials.

Abstract: An acetabular trialing system has a trial cup including a body comprising an outer surface, a part-spherical inner surface and a rim extending between the inner and outer surface with a plurality of spaced inwardly resiliently deflectable rim members each connected at a first end to the body outer surface. The part-spherical inner surface has a plurality of spaced resilient deflectable bearing members each forming part of the body part-spherical inner surface. The bearing members have a first end deflectable towards the body outer surface. Upon inward deflection, one of the plurality of deflectable rim members is capable of contacting the first end of a corresponding one of the plurality of deflectable bearing members and moving the bearing member towards the body outer surface and into contact an electrical signaling device mounted on the body intermediate the outer surface thereof and the deflectable bearing member.

Abstract: The invention includes an osseointegrated mount and electrical connector, suitable for providing neural control and sensory feedback for an advanced prosthetic limb. The device provides a channel in which a lead wire from the peripheral nerve interface can travel from the electrical connector down the side of the device or within the device to limit potential sites of infection to a single transcutaneous breach. The channel allows for a silicone barrier to be installed between the internal and external components.

Abstract: A stent removal device for removing or repositioning a stent from within a lumen is provided. The stent typically comprises at least one element arranged circumferentially about the stent. The stent removal device includes a tube positioned within the lumen proximate to the stent, wherein the tube is capable of receiving at least a portion of the stent. The stent removal device also includes a pusher positioned within the tube capable of engaging the stent and/or the element. The stent removal device further includes a hook positioned within the tube and including a hook member capable of engaging the element such that force applied to the hook causes the stent to purse string.

Abstract: A system for endoluminally delivering and deploying a prosthesis includes a prosthesis comprising a self-expanding stent and a cover for retaining at least a portion of the self-expanding stent. The stent is biased into contact with an inner surface of the cover. The inner surface has a hardness that is equal to or greater than the hardness of the stent. Additional aspects of the invention are disclosed and include a method of manufacturing an endoluminal prosthesis delivery and deployment system.

Abstract: A process for crimping stents includes a multi-stage process producing a desired stent retention and crimped profile in a reduced amount of time. The process achieves results by utilizing particular combinations of heat and pressure during the crimping process, which was found to produce the desired results.

Abstract: A system for treating a body vessel may include a delivery device and a prosthesis retained on the delivery device. The prosthesis may include a main body and first and second legs each extending from the main body. The main body may include a lumen, and the first leg may include a lumen in fluid communication with the lumen of the main body. The second leg may include a tubular graft body and a stent attached to the graft body. The prosthesis may have a predeployment configuration in which the graft body of the second leg is inverted into and positioned within the lumen of the first leg, and the stent is positioned outside of the inverted graft body. The prosthesis may have a deployed configuration in which the second leg extends outward from the main body, and the stent is positioned within a lumen of the graft body.

Abstract: A delivery device for deploying and resheathing an expandable prosthesis such as a stent. The delivery device includes a movable outer sheath and a fixed pusher/holder member that are configured for the sheath to retract in a proximal direction to release and/or to extend distally to resheath the stent. The device includes a spring-tensioned anti-backlash mechanism to accommodate any backlash elongation and/or compression of the pusher/holder member and sheath.

Abstract: The stent graft delivery device includes a shaft on which the stent graft is placed on the distal side; a sheath which is slidable outside of the shaft; a handle which is provided on the proximal side of the shaft and the sheath; and an operation unit which is provided with a switch mechanism. When a rotating member is rotated, while in a state of pressing a switch member of the switch mechanism inward, the sheath moves backward and the shaft moves forward using the handle as a reference.

Abstract: A stent delivery system, a core assembly, and methods of operating the same are provided. The delivery system can comprise a catheter and the core assembly. The core assembly can comprise a constraining member, protruding member, a core member, and a stent extending along the core member. The tubular constraining member can be spaced apart from the core member and define a capture area. The protruding member can be disposed along the core member at least partially distal of the capture area. The stent can have a first portion disposed within the capture area and a second portion, distal to the first portion, extending across or over an outer surface of the protruding member so that the protruding member and the constraining member cooperate to inhibit expansion of the first portion of the stent.

Abstract: An orthopedic brace may include a main panel made of a flexible, breathable elastic fabric, such as perforated neoprene or AIRPRENE.® The main body panel includes a a fastening implement, such as hook-and-loop fasteners to secure the main body panel in an encircling position on or near a subject area of the human body. The brace may a shank embedded in the main panel to add rigidity in one or more areas. At least two adjustable strap loops may cooperate with the shank to provide targeted and precise compressive forces to the treatment area when the brace is installed. The strap loops may be anchored at one end to the main panel, extend through sliding rings and may be provided with fasteners at another end to adjustably engage corresponding fastening pads on the main body panel. The adjustable strap loops, rings and shank cooperate to provide for the targeted and precise application and distribution of pressure force to the treatment area.

Abstract: A trunk support device (100) is configurable to be worn by a person to reduce the muscle forces in the person's back during forward bending. The device (100), among other things, includes: a waist strap (102) which is configurable to be coupled to the person waist; a chest support (104) which is configurable to be coupled to the person's chest and capable of pushing against the person chest; and first and second torque generators (106) coupled to the chest support (104) and the waist strap (102) and capable of providing a resistance torque between them. In operation, when a person wearing the device (100) bends forward, at least one of the torque generators (106) imposes a torque between the chest support (104) and the waist strap (102), causing the chest support (104) to impose a force onto the person's chest backwardly and the waist strap (102) to impose a force onto the person's hip.

Abstract: A detachable orthopedic sling for treatment of a user's spine is provided. The detachable orthopedic sling includes first and second adjustable sections, first and second handholds, and a strap. The first and second adjustable sections permit adjustment of their respective lengths. The first and second adjustable sections extend from one or more attachment rings to the first and second handholds. The strap permits adjustment of its length and may be positioned by a user around his torso, under his arms, and across his back. The detachable orthopedic sling may be mechanically coupled to a support structure using the attachment rings and allows the user to hang from the sling to provide traction treatment of the user's spine.

Abstract: The product improves nasal passage air flow. The product may be a strip that comprises a flexible resilient material, with at least a portion of the bottom surface comprising an adhesive surface on each end. The strip may serve to dilate a user's nasal passage when the first end of the strip is secured using the first adhesive bottom surface to be proximate to an alar facial groove of the user's nose, with the second end of the strip being puled up at a slight angle and laterally to achieve desired nasal passage expansion and thereafter being secured to the user's face. The size of the strip may be larger for additional benefits and have anti-glare and/or anti-reflective features.

Abstract: The body-adhesive kinesiology tape includes a strip of kinesiology tape. The strip of kinesiology tape includes a first end and a second end where the second end is opposite the first end. The body-adhesive kinesiology tape also includes a longitudinal cut in the strip of kinesiology tape extending from the first end to a pre-determined distance from the second end and adhesive on a first surface of the strip of kinesiology tape. The adhesive is configured to adhere the strip of kinesiology tape to a human body. The body-adhesive kinesiology tape further includes a backing material on the first surface of the strip of kinesiology tape. The backing material is configured to cover the adhesive and protect the adhesive from drying until a user is ready to apply the strip of kinesiology tape to the human body.

Abstract: An orthosis has an elastic compressive distal portion, extending upwards from the ankle, associated with an adjacent rigid splint proximal portion, and enveloping the region of the calf between the level of the point where the Achilles tendon joins the calf muscles and the level located below the tibial tuberosity, the rigid splint proximal portion being an essentially non-elastic, deformable tubular portion made by placing the orthosis onto a template representative of the morphology of the patient's calf, applying in situ on the orthosis, in the region of the splint proximal portion, a hardenable biocompatible resin, hardening the resin with the orthosis maintained on the template, and removing the orthosis in its finished state.

Abstract: The present invention relates to a ring for enhancing male functions, and comprises: a first sectioned ring member; a second sectioned ring member having one end portion which is rotatably coupled to one end portion of the first sectioned ring member; and a coupling member, which is rotatably provided on the other end portion of the second sectioned ring member, and which couples to the other end portion of the first sectioned ring member so as to be separable, wherein the coupling member comprises a coupling plate, which is hinged-coupled to the other end of the second sectioned ring member, and a stopper protrusion portion that is protrudingly formed on the inner surface of the coupling plate, and wherein the first sectioned ring member comprises, on the other end portion thereof, a groove portion, and a hooking rod, which is provided on the groove, for coupling to the stopper protrusion by means of hooking.

Abstract: Various embodiments disclose a urine collection device. In one embodiment, a urine collection device includes a neck and a collection bag. The collection bag includes a main body disposed below the neck. The main body extends laterally away from the neck and is continuous with the neck. The urine collection device further includes a retention band that is disposed in an upper region of the neck. The retention band is formed from and circumscribes the upper region of the neck. The retention band includes a first fastening mechanism disposed on a first portion of the neck and a second fastening mechanism disposed on a second portion of the neck. The first fastening mechanism is configured to releasably mate with the second fastening mechanism when the first portion of the neck is overlapped with the second portion of the neck.

Abstract: An inserter for placing a T-shaped intrauterine device inside a patient's uterus and a T-shaped intrauterine device are disclosed. The inserter includes a sleeve part and a plunger part, the sleeve part includes a tube and a first engaging member and the plunger part includes a rod, a handle attached to the rod and a second engaging member. The first and the second engaging members are configured for reversibly engaging the sleeve part and the plunger part to temporarily lock the relative position between the tube and the rod. The T-shaped intrauterine device includes a pair of wings having a relaxed extended configuration and a contracted folded configuration and an elongated contraceptive body suspended from a junction between the wings.

Abstract: The present invention relates to methods for use in the selective disruption of lipid-rich cells by controlled cooling. The present invention further relates to a device for use in carrying out the methods for selective disruption of lipid-rich cells by controlled cooling.

Abstract: A self-contained helical air distribution system for the body of an individual which can distribute air over both the chest and back of the individual, the system including a battery operated blower fan in communication with the plenum and manifold, the manifold having a plurality of tubular distribution conduits, each conduit having a capped end, the conduits extending over the chest and back of the body, the conduits formed with a spiral helix cut allowing the tubular conduits to react to the motion of the human body, the spiral helix cuts reacting to such movement, thereby allowing air to selectively escape from the expansion of these cuts providing a cooling and evaporate effect. With slight adaptation the air distribution system can distribute heated air and also be used to control the ambient temperature about inanimate objects, such as computers, electronic instruments, windshields, and car seats.

Abstract: The present invention relates to a system for keeping a patient warm, particularly a veterinary patient, during care. An apparatus is provided for delivering conditioned air across a barrier, such as a wire cage, to a blanket arrangement for providing conditioned air to the patient. A first duct and a second duct part are provided either side of the barrier mounted together across the barrier, so a duct is provided for ducting conditioned air across the barrier.

Abstract: Methods and devices are disclosed herein that generally involve applying thermal therapy to tissue (e.g., localized cooling or heating of tissue), and in particular applying thermal therapy to the spinal canal, tissue disposed within the spinal canal, and/or nerve roots extending from the spinal canal. In some embodiments, tissue can be cooled or heated by implanting or positioning a thermal device in proximity to the targeted tissue. A number of exemplary thermal devices are disclosed, including bone anchors, inserts for use with bone anchors, K-wires, bone anchor extensions or towers, cross-connectors, spinous process plates, spinal rods, pedicle markers, bone taps, drill bits, bone plugs, bone plates, clamps, interbody or disc implants, thermal pads, and tubing loops. The thermal device can be left in place following surgery to facilitate application of post-surgical thermal therapy. In some embodiments, the thermal device can be removed post-surgery in a minimally- or non-invasive manner.

Abstract: In various embodiments, a drug-delivery device includes one or more reservoirs that may each contain a therapeutic agent for delivery to a patient.

Abstract: The present technology relates to an apparatus for intraocular injection comprising a plate adapted for being brought into contact with an eye and a guide operable to guide a needle into the interior of an eye, characterized in that it comprises means for displacing a superficial layer (1) of the eye over an underlying layer (2) of the eye as the plate is brought into contact with the eye before the needle is guided into the interior of the eye.

Abstract: Improvements in devices, systems and methods for non-invasively lowering intra-ocular pressure (IOP). In examples, the device applies non-invasive, focal, mechanical oscillation to the limbal region at a low amplitude and frequency, targeting the trabecular meshwork to restore outflow function and lower IOP.

Abstract: A phacoemulsification probe includes a first portion for interconnecting the probe with a phacoemulsification machine. A probe tip has a first end connected with the first portion and a second end curved up to a predetermined angle. The probe tip defines a channel therein for aspirating material through the probe tip from a surgical region.

Abstract: An optical surgical probe includes a cannula; a light guide within the cannula, configured to receive a light beam from the light source, to guide the light beam to a distal end of the light guide, and to emit the light beam at the distal end of the light guide; and a multi-spot generator at a distal end of the cannula, the multi-spot generator having a faceted proximal surface with oblique facets, configured to receive the light beam emitted at the distal end of the light guide and to split the received light beam into multiple beam-components, and a distal surface through which the multiple beam-components exit the multi-spot generator, wherein the proximal surface of the multi-spot generator is micro-structured with a modulation length smaller than a wavelength of the light beam in order to reduce the reflectance of light back into the probe.

Abstract: An ophthalmic laser treatment apparatus for treating an eye including: an irradiation unit including a laser source, and a scanner for scanning an irradiation spot from the laser source onto a tissue of the eye in two dimensions; a memory for storing a plurality of predetermined irradiation patterns in each of which a plurality of the irradiation spots are arranged in a predetermined arrangement; an irradiation pattern selecting unit including a switch for inputting a signal to select a pattern from the patterns stored in the memory; an pattern changing unit including a switch for inputting a signal to change part of the arrangement of the irradiation pattern in which irradiation spots are arranged on the basis of the selected irradiation pattern; and a control unit for controlling driving of the irradiation unit to sequentially irradiate the beam based on the irradiation pattern changed by the pattern changing unit.

Abstract: A stretch laminate includes a first layer including a skinned or skinless elastomer film, the first layer having a surface, and a second layer including a nonwoven material, the second layer having a basis weight of less than about 25 gsm and a surface that is attached to the surface of the first layer. The elastomer film has a strength of an engineering tensile strength, at an engineering strain rate of about 600/s, of at least one of about greater than about 14 MPa for a plain specimen or about greater than about 7 MPa for a notched specimen. A method of making the stretch laminate and an absorbent article having at least one region defined by the stretch laminate are also provided.

Abstract: A permanently closed containment pant includes an elastically extensible chassis and a sling positioned within the chassis. The sling is joined to the front waist region and the back waist region. The sling includes a fluid-impervious base sheet and a containment flap joined with the base sheet to create a fluid-impervious pouch. The sling also includes a first transition and a second transition that are elastically extensible in a longitudinal direction and in a transverse direction. The base sheet is a fabric laminated with polyurethane and the containment flap is a fabric laminated with polyurethane. The polyurethane surface of the base sheet is ultrasonically joined in facing relationship with the polyurethane surface of the containment flap. The permanently closed containment pant is substantially devoid of an integrated absorbent core.

Abstract: A method including: a step of forming depressions and protrusions on a first continuous sheet between a first roll and a second roll; a placement step of placing a plurality of granular particles in depressed portions of the depressions and protrusions of the first continuous sheet; a step of laying a second continuous sheet on the first continuous sheet, thereby forming a sandwich structure; and a step of bonding the two sheets with each other along protruding portions of the depressions and protrusions of the first continuous sheet, wherein a circumferential velocity of the second roll is greater than a circumferential velocity of the first roll.

Abstract: A method for making apertures in a web comprising providing a precursor web material; providing a pair of counter-rotating, intermeshing rollers, wherein a first roller comprises circumferentially-extending ridges and grooves, and a second roller comprises teeth being tapered from a base and a tip, the teeth being joined to the second roller at the base, the base of the tooth having a cross-sectional length dimension greater than a cross-sectional width dimension; and moving the web material through a nip of the counter-rotating, intermeshing rollers; wherein apertures are formed in the precursor web material as the teeth on one of the rollers intermesh with grooves on the other of the rollers.

Abstract: A method of manufacturing a tampon comprises the steps of at least partially overlaying a web of base material with a web of absorbent material. The web of absorbent material is secured to the web of base material with a first securement. At least one of the web of base material and the web of absorbent material is folded after the first securement. The web of absorbent material is further secured to the web of base material with a second securement that is a stronger securement than the first securement. The web of absorbent material and the web of base material together define a web of cover material. The web of cover material is applied to an absorbent structure. The web of cover material and the absorbent structure is manipulated such that the web of cover material extends about a circumference of the absorbent structure to form a tampon.

Abstract: The present application discloses and claims an absorbent article which utilizes a stabilizing member within the article having a design which is intended to reduce the amount of vertical bunching of the product when the product is subjected to lateral compressive forces as are commonly exerted by a wearer during use of the article.

Abstract: An outer covering sheet (4) of a pants-type disposable diaper (1) has a front part and a back part (403) to be positioned on a front side and a back side of a wearer, and a middle part lying between the front and back parts. An absorbent body (20) is attached on the outer covering sheet (4) to absorb excrement from the wearer. Both end portions of the absorbent body, positioned in the front part and the back part (403), are folded toward the inner surface (40) of the outer covering sheet (4) and bonded on the inner surface (40). It is therefore possible to prevent skin of the wearer from being irritated by edges (241) of the end portions of the absorbent body (20) when the disposable diaper (1) is worn.

Abstract: An array of personal care absorbent articles includes a menstrual absorbent article having a perimeter, a first transverse midline, a first minimum width line, and a menstrual absorbent layer having a menstrual absorbent shape, the perimeter defining a first article shape and a first article size. The array also includes an incontinence absorbent article having a perimeter, a second transverse midline a second minimum width line, and an incontinence absorbent layer having an incontinence absorbent shape, the perimeter defining a second article shape and a second article size, wherein the first article shape is substantially the same as the second article shape, and wherein the first article size is substantially the same as the second article size.

Abstract: An absorbent article including a fluid permeable topsheet, a fluid impermeable backsheet and an absorbent core enclosed between the topsheet and the backsheet. The absorbent core includes a first absorbent layer having an opening extending therethrough. A fluid flow control structure is arranged between the first absorbent layer and the backsheet. The fluid flow control structure is a layered structure including a non-perforated fibrous polymeric layer and a first perforated polymeric layer having a basis weight of from 50 g/m2 to 100 g/m2.

Abstract: An individual packing product that makes it difficult to see an absorbent product disposed therein, not staining other individual packing products, and easy to put in a bag or pocket and carry. In the individual packing product, the absorbent product having an adhesive portion in a non-skin contact region is packed with a packing sheet. The absorbent product is fixed to the inner side of the packing sheet with the adhesive portion being disposed therebetween, the packing sheet is folded with the absorbent product being disposed therein, the packing sheet has a separable colored portion on the inner side thereof, and although the colored portion can be seen from the outside of the individual packing product, the absorbent product cannot be seen from the outside of the individual packing product.

Abstract: A paramedic chair carrier is provided comprising a main frame and a sliding frame slidably carried by the main frame so as to be slidable between an extended position and a retracted position relative to the main frame. A gas spring acts between the main frame and the sliding frame to bias the sliding frame toward the retracted position. A chair support hook on the sliding frame supports the paramedic chair and a chair handle latch is carried by the main frame for releasably retaining the handle of the paramedic chair. A locking latch system comprising a first lock component carried by the sliding frame and a second lock component carried by the main frame releasably locks the sliding frame in the retracted position.

Abstract: The invention is directed to a mobile medical facility capable of treating, diagnosing and performing minor surgery on multiple patients at one time. In general, the facility includes a health care area which is interchangeable between a first transportable configuration and a second, operational configuration. In the operational configuration, the health care area is expanded and capable of providing general care or diagnostic facilities to multiple patients as well as registration, counseling and triage to at least one patient. Preferable a row of patient treatment bays are provided with intake, counseling and triage cubicles and storage areas.

Abstract: A wheelchair includes a chassis; first and second wheels coupled to the opposites sides of the chassis; a front caster; and a rear caster. The chassis includes a base plate; a back plate; first and second side plates; a rear plate; and a seat coupled to the back plate and the first and second side plates opposite the base plate.