Abstract: A method of implanting a humeral component includes accessing a humerus and resecting a head portion of the humerus to form a resected surface. The method further includes selecting a first combination sizer and guide device having an outer surface sized complementary to a desired implant head size, positioning the selected first combination sizer and guide device on the resected surface, guiding placement of a guide pin in the humerus with the first combination sizer and guide device, guiding a reamer with the placed guide pin to form a reamed cavity in the humerus, positioning an anchoring portion of a humeral implant base portion in the reamed cavity, positioning the first combination sizer and guide device on the base portion, removing the first combination sizer and guide device from the base portion, and positioning an implant head on the base portion.

Abstract: A prosthesis, radiation bolus, pre-surgical model, or burn mask formed using a rapid prototyping device, such as a three-dimensional printer. In some exemplary aspects, the prosthesis includes a scaffolding and a coating at least partially covering the scaffolding. Methods and systems for forming the prosthesis, radiation bolus, pre-surgical model, or burn mask are also provided.

Abstract: A digit for a prosthetic hand is provided. The digit has a base member (12) attachable to the hand and at least one digit member (18) pivotably connected to the base member. The at least one digit member (18) has a digit tip (22) remote from the base member (12), and the digit member is at least partially covered with at least one conductive substance (26,40) which defines a conductive path which leads from the digit tip towards the base member. A method of manufacturing such a digit is also provided.

Abstract: Prosthetic hand (1) with a wrist (13) and provided with a hand palm (2) and fingers (4) attached to the hand palm (2), wherein the hand palm (2) and fingers (4) comprise bars (5) and joints (6) connecting the bars (5) forming a construction (7) supported by the wrist (13), wherein said bars (5) occupy a position with reference to each other de-pending on an external load applied to the construction (7), wherein a reaction force for said load applied to the construction (7) is provided by or through the wrist (13), and wherein the construction (7) has an unloaded position wherein the fingers (4) are stretched and a plurality of loaded positions corresponding to loads applied to an inner side of the hand (1) wherein the construction (7) is deflected from the unloaded position wherein the fingers (4) are stretched into a series of loaded positions in which the fingers (4) are flexed into increasingly bonded positions so as to eventually close the hand (1), and that said construction (7) is provided with a lockin

Abstract: Prosthetic feet that provide improved rollover and performance are provided. A prosthetic foot can include a lower foot member extending from a heel end to a toe end, a second foot member disposed above the lower foot member, and an optional third foot member disposed above the second foot member. The second foot member is tapered such that its thickness decreases toward the proximal end. Optionally, the second foot member can taper toward its distal end as well as toward its proximal end from an intermediate location on the second foot member. The third foot member can be tapered such that its thickness decreases toward the distal end. There can be a gap between a distal end of the third foot member and the second foot member that closes during dorsiflexion of the prosthetic foot during use and provides dynamic stiffness control to the prosthetic foot.

Abstract: A prosthetic system includes a prosthetic foot with a foot member defining a first end portion, a second end portion, and an intermediate portion defining a curvature and extending between the first and second end portions. A pump mechanism is coupled to the foot member. The pump mechanism includes a housing defining a cavity, and a membrane situated in the cavity. The pump mechanism is movable between an original configuration and an expanded configuration. A movable member includes a first portion coupled to the membrane and a second portion arranged to slidably engage the foot member. Relative movement between the first and second end portions moves the first portion of the movable member relative to the housing and slides the second portion along a length of the foot member to shift the pump mechanism between the original and expanded configurations.

Abstract: A disarticulated compression socket configured to secure a residual limb. The disarticulated compression socket may include a rigid socket frame having one or more compression apertures each having one or more disarticulated compression inserts. Each disarticulated compression insert may be coupled with, and responsive to, a compression actuator configured to adjust the disarticulated compression insert individually, or in concert. In one preferred embodiment, at least one compression actuator may be coupled with one, or a plurality of disarticulated compression inserts and further configured to retract and/or expand the coupled disarticulated compression inserts securing the residual limb within said socket frame. Control of the compression actuators may be manual or automatic in response to a signal from a sensor.

Abstract: A prosthetic connector system for use with a prosthetic socket having a distal end includes a plate defining a plurality of holes and attachable to the distal end of the prosthetic socket. A component is removably attachable to the plate via the plurality of holes and arranged to connect a prosthesis to the prosthetic socket. The plate defines an outer periphery having an asymmetrical configuration contoured to substantially correspond to at least a portion of the component when the component is attached to the plate via at least some of the holes.

Abstract: An elastic ring, defining an inner opening, an outer contour and an annular bearing surface between the inner opening and the outer contour. The ring is deformable between a rest position and an insertion position in which the inner opening has a diameter greater than its diameter in the rest position. The ring is also elastically biased towards the rest position. The ring includes at least three strands passing through the ring, each strand having a first end and a second end positioned on the outer contour, the inner contour of the opening being defined by a portion of each strand and having a pseudo-polygonal shape.

Abstract: The present invention concerns a self-expanding implant device comprising a proximal portion at a first longitudinal end, a distal portion at a second longitudinal opposite the first longitudinal end, and a connecting portion between the proximal portion and the distal portion, wherein the proximal portion and the distal portion each comprise a radially self-expanding structure, wherein the connecting portion comprises longitudinally oriented bendable struts, preferably at least 4 struts, more preferably 6 struts or more, which connect the self-expanding structure of the proximal portion with the self-expanding structure of the distal portion, wherein in a fully expanded state, the implant device comprises a maximum implant diameter along a direction perpendicular to the longitudinal direction and wherein the struts of the connecting portion comprise a strut length along the longitudinal direction, characterized in that the strut length is such that when the self-expanding structure of the proximal portion is

Abstract: A stent comprising a stent body and a plurality of cells is disclosed. Each cell includes two structural members extending in an undulating pattern. Each structural member includes a plurality of cell segments defining a plurality of peaks and valleys therebetween. A first segment and a second segment defining a first peak, the second segment and a third segment defining a first valley, the third segment and a fourth segment defining a second peak, the fourth segment and a fifth segment defining a second valley, the fifth segment and a sixth segment defining a third peak. The first peak, the second peak and the first valley include a first radius of curvature. The third peak and the second valley include a second radius of curvature. The first radius of curvature is larger than the second radius of curvature.

Abstract: An improved medical device reduces the loss of longitudinal length during expansion of a stent-graft from a compressed state to an expanded state. For example, the stent-graft is placed over a cover that provides resistance to expansion of the balloon during inflation, which reduces longitudinal compressing forces exerted on the stent-graft.

Abstract: Catheter systems and methods for deployment of an endoluminal prosthesis in a body lumen of a patient while maintaining control of a position of the endoluminal prosthesis during the deployment process. Some of the systems and methods are configured to minimize frictional forces of components of the catheter systems during deployment procedures.

Abstract: A medical instrument is provided including, an expandable tip which is embedded within a sheath. The expandable tip comprises a plurality of fingers which extend distally from the embedded portion. The plurality of fingers are heat set in a first position so that the distal ends of the fingers define a distal opening, where the distal opening has a smaller diameter than the embedded portion of the expandable tip. The plurality of fingers is reversibly expandable to a second position, creating a larger distal opening to deploy an expandable accessory.

Abstract: A joint angle adjustment mechanism is provided. A base has a center and two side boards opposite to each other, and at least one of the two side boards has toothed recesses arranged curvedly and open toward the center. Two connecting members are respectively connected to the base, and at least one of the two connecting members is pivoted to the base. At least one adjustment mechanism is axially pivoted to the base about the center, each said adjustment mechanism includes a positioning assembly including a slidable seat, a positioning member and an elastic member within the slidable seat, the positioning member is slidably arranged within the slidable seat and optionally moves radially to be engaged with or disengaged from one of the toothed recesses, the elastic member radially urges the positioning member to engage with one of the toothed recesses.

Abstract: A guide joint (1) and a joint orthosis (2) provided with the guide joint for supporting and guiding an anatomical joint (7). The guide joint (1) has a first joint member (3) and a second joint member (4), and the joint members (3, 4) are connected to one another by a first linear guide (5) and a second linear guide (6). Each of the linear guides (5,6) has a guide track (10, 11) formed in the second joint member (4) as a slot or groove, in which in each case a sliding element (12, 13) arranged in the first joint member (3) engages, wherein the guide tracks (10, 11) intersect. The two sliding elements (12, 13) are spatially separate and spaced apart and protrude from a lateral surface of the first joint member (3).

Abstract: Variable stiffness devices and methods of their use are provided. In some embodiments, a variable stiffness device comprises an inner member defining a compartment for receiving an actuating fluid; an outer member disposed around the inner member; and a granular medium disposed between the inner member and the outer member; wherein the inner member is being moveable in a radial direction from a relaxed state to an expanded state by introducing the actuating fluid into the compartment of the inner member to compress the granular medium against the outer member to increase the stiffness of the device.

Abstract: This relates to a device that combines ultrasound energy, electrical energy, light, and vacuum to improve the general health function of the penis and the vagina. It is intended to be safe, easy to use way to increase and improve the vascular supply to the penis and vagina. A system will comprise a power source, vacuum pump and a stimulatory device. The male device comprises a tubular receptacle including an inner tube and an outer tube; the inner tube having electrodes, ultrasound transducers, and light sources, all attached to the inner tube to direct their energy to the inside, the inner tube positioned within the outer tube. The front is closed by a cup that fits on and receives the outer tube rim. The back is closed by a rear base assembly that receives an end of the inner tube so the inner tube does not contact the outer tube.

Abstract: A body side member of an ostomy appliance having backing film forming a distal surface, the distal surface including one or more individual pockets containing a moldable material that can exit the pockets.

Abstract: An apparatus for human waste collection includes a containment component that includes an enclosed area that has a female receptacle for capturing of excrement. The containment component having a female receptacle interfaced to the enclosed area. A patient component is included for removably attaching to a user. The patient component has an opening for interfacing with an anus of the user and the opening is in fluid communication with a guide barrel. The guide barrel is configured to mate with the female receptacle of the containment component. The patient component has an adhesive material for removably adhering to the user at a location of the anus of the user.

Abstract: Disclosed herein are mandibular advancement devices comprising an upper splint and a lower splint, where the upper splint comprises one or more upper fins, where each upper fin is located at a distance UD from back of the upper splint; the lower splints comprise one or more lower fins, where each lower fin is located at a distance LD from back of the lower splint; where the position of the upper and lower fins is unchangeable. Also disclosed are methods of reducing partial constriction of airway during sleep for a patient, the method comprising identifying a patient in need thereof; and administering to the patient the disclosed mandibular advancement device. Also disclosed are methods of manufacturing a mandibular advancement device, the method comprising obtaining measurements from a patient's dentition; digitally designing a mandibular advancement device; and milling the mandibular advancement device.

Abstract: A device sized and shaped for alleviating organ prolapse when inserted into a vagina, comprising: (a) an adjustably flexible, substantially planar ring provided with at least one opposing snapping element; (b) a central rod extending at least partially through the ring transverse to the snapping elements, where the central rod is provided with counterpart slots configured for insertion of the snapping elements therein; and, (c) a connection block, co-axial with the central rod and slidable thereover to transition the device from an expanded state to a collapsed state, configured with slots which align with the counterpart slots of the central rod for passage of at least one snapping element therethrough when the device is in the collapsed state.

Abstract: A device sized and shaped for alleviating pelvic organ prolapse when inserted into a vagina, comprising: a treatment rendering portion configured to be adjustable between a first, collapsed state and a second, expanded state, where the second expanded state extends substantially in three dimensions.

Abstract: A portable heating/cooling device for clinical hypo/hyperthermia with cuffs especially designed for arterial cooling/heating for raising or lowering the body temperature of a patient is operable by battery power or a wide range of available external power, and is usable in the field or in medical transport where such external power sources are not available. The small size, weight, and robust nature of the device allows it to be transported with the patient without the need for additional conveying devices.

Abstract: Disclosed is an apparatus and method for treating a number of eye conditions of a user including dry eye syndrome or burns to the eyes. The apparatus include a pair of protective close fitting glasses flexibly connected to form a goggle to securely cover a pair of eyes of the user, a frame structure including input means is provided around the pair of protective close fitting glasses, one or more diffuser in fluid communication with the frame structure to provide heat, moisture content and the medications to the eyes of the user, and one or more mode selector means configured on the diffuser, and/or provided as a controller for selecting a desired operational mode for providing a desired amount of heat, moisture and the medication to the eyes of the user to treat the number of eye conditions including dry eye syndrome or burns to the eyes.

Abstract: Vitreoretinal instruments and methods related thereto are disclosed herein. The disclosure describes various example vitreoretinal instruments having various aspirating port configurations. A vitreoretinal instrument may include a handle and a cannula coupled to the handle. The cannula may include a straight portion and a curved portion. The curved portion may be configurable between a straight configuration and a curved configuration. The curved configuration may include a first curved portion having a curvature defined by a first radius. The curved configuration may include a second curved portion having a curvature defined by a second radius different from the first radius. The curved portion may further include one or more ports formed in the curved portion.

Abstract: Methods and systems for performing laser-assisted surgery on an eye form one or more small anchoring capsulotomies in the lens capsule of the eye. The one or more anchoring capsulotomies are configured to accommodate corresponding anchoring features of an intraocular lens and/or to accommodate one or more drug-eluting members. A method for performing laser-assisted eye surgery on an eye having a lens capsule includes forming an anchoring capsulotomy in the lens capsule and coupling an anchoring feature of the intraocular lens with the anchoring capsulotomy. The anchoring capsulotomy is formed by using a laser to incise the lens capsule. The anchoring feature can protrude transverse to a surface of the intraocular lens that interfaces with the lens capsule adjacent to the anchoring capsulotomy.

Abstract: Removable goggle lens system including a sequentially-stacked set of lenses each of the lenses having a front-face, a back-face, a thickness, and a finger-tab. Each of the lenses are defined by the front-face, the back-face, the front-face, and the back-face separated by the thickness; and the finger-tab formed as an extension of the thickness such that a wearer-user can remove each of the lenses sequentially as desired approaching a main lens of a host goggle as sequentially removed.

Abstract: In accordance with an aspect of the present invention, there is provided a wound dressing with elastic properties for use with a human or an animal. The wound dressing includes a plurality of individual segments, each segment connected to at least one other segment by an elastic connector, and each segment having at least two perforated layers, with at least one layer having a plurality of protrusions. The wound dressing further includes a plurality of spacing elements, with each spacing element disposed between adjacent segments and retained by either the adjacent segments or the elastic connector.

Abstract: A wound packing material, particularly suitable for use in negative pressure wound therapy, comprising a porous material admixed with a chemoattractant. This disclosure further provides methods of manufacturing the wound packing material, and therapeutic methods of using the wound packing material.

Abstract: A dressing for an open wound includes a cover layer dimensioned for positioning relative to a wound bed. The cover layer permits an evacuation of the space around the wound bed such that a sub-atmospheric pressure may be established to stimulate healing and facilitate the removal of fluid from the wound. Multiple performance zones in the cover layer allow the wound dressing to remain in position through repeated cycles of evacuation without placing undue strain on the wound bed. An outer peripheral zone may include a high peal-strength adhesive while an intermediate zone may include a shear resistant adhesive. A central zone may be devoid of any coating to maximize moisture transmission through cover layer.

Abstract: Disclosed embodiments relate to apparatuses for wound treatment. In certain embodiments, a negative pressure wound therapy apparatus includes one or more electronic components configured to be incorporated into layers of the wound dressing or integrated on top of the wound dressing. In some embodiments, a negative pressure source is incorporated into the wound dressing. The negative pressure source can be sealed between two moisture vapor permeable cover layers or enclosed in a moisture vapor permeable pouch, and may be received in a recess of an absorbent layer or spacer layer of a wound dressing apparatus.

Abstract: A pulpless core is provided with flexibility for superabsorbent expansion by using elastic strands stretched and coupled to a nonwoven layer, and then relaxed partially to create receiving valleys (puckers) and the puckers are provided with superabsorbent polymer, and then a layer of nonwoven or acquisition film can be coupled on top of nonwoven/elastic/sap carrier layers to create an absorbent core laminate. A tubular core can be created and placed into a product with or without additional absorbent material between adjacent tubular members. A printed back sheet corresponding to either the tubular core shape, or void spaces between tubular members can be provide. A forming drum pocket can be profiled to match tube or tube shaped zones and elastic placements between adjacent tubes, if desired.

Abstract: The present invention relates to a method for fabricating absorbent article having multiple layers, and deformed zones of targeted performance, and colored regions, the method comprising the steps of forming discrete features on at least one layer, printing colored regions on at least one layer, integrating multiple layers to form an absorbent assembly, and cutting the absorbent assembly into individual absorbent articles, wherein the steps are carried out continuously.

Abstract: An absorbent sheet manufacturing apparatus has a particle collision surface (224) that extends downward from a cylinder outer surface (211) in between the lowermost part of a supply cylinder (21) and a second sheet conveying roller (41). Some of the particles emitted forward in the rotation direction of the supply cylinder (21) from recessed supply portions (212) that have passed a first cover part (221) collide with the particle collision surface (224), and the colliding particles are guided by the particle collision surface (224) onto a first sheet member (91). This suppresses direct collision of particles emitted from the supply cylinder (21) with a second sheet member (92) on the second sheet conveying roller (41). Scattering of particles that have collided with the second sheet member (92) around the first sheet member (91) and the second sheet member (92) is thus suppressed.

Abstract: A moisture management apparatus monitors an area for moisture events and wirelessly transmits moisture-related information to one or more notification devices. An embodiment of the moisture management apparatus includes a substrate and one or more sensors supported by the substrate. The sensor(s) emit wireless signals indicative of the moisture-related information. A sensor event communication system forwards the sensor signals to another device, such as a notification device. The sensor event communication system may monitor other types of patient events. Portions of the moisture management apparatus and/or the moisture event communication system may be embodied in a patient support apparatus, such as a bed.

Abstract: An absorbent article such as disposable diaper, training pant, and adult incontinence undergarment comprising superabsorbent polymer particles able to absorb and contain body exudates having improved absorption properties and, therefore, reduce leakage, especially at the first gush, i.e. when the article starts to be wetted.

Abstract: A sheet-like article (1) for an absorbent article of the invention includes a plurality of absorbent units (4), each including: a long base portion (2); and water-absorbent polymer particles (3) that are fixed to a surface of first side of the long base portion (2). In the sheet-like article (1), the absorbent units (4) are arranged such that the longitudinal direction thereof is oriented in one direction. When the water-absorbent polymer particles (3) absorb a liquid, the water-absorbent polymer particles (3) swell beyond the lateral side edge portions (2s), of the long base portion (2), that extend along the longitudinal direction, and a position, in the thickness direction, of each long base portion is varied from the position thereof before absorbing the liquid.

Abstract: Problem to be solved: protecting a menstrual tampon (2) from mechanical damage, from contamination and moisture, and the problem with carrying it discreetly. Solution to the problem: a case (1) for tampons (2) consisting of a rigid body, inside of which there is stored at least a single row of tampons (2) arranged in parallel, provided at the bottom closed end (4) with a dispensing means acting on the outer tampon (2) of the row of tampons (2) and is provided at the open top end (5) with a holder (6) for retaining the tampon (2) in the top end (5) for easy and gradual removal.

Abstract: A wound protection device can include a frame having a plurality of first members and a plurality of second members. The first members can be spaced relative to each other. The second members can be spaced relative to each other and can be coupled to the first members. The first members and the second members can define a plurality of a gaps through which a fluid can enter the frame. The frame can be configured to circumscribe a wound.

Abstract: A patient trolley configured for transporting a patient to a target modality includes a top portion having a top surface and an overhang area along at least one side of the top portion, a bottom portion supporting the top portion, and a side rail coupled to the top portion for movement between a deployed position and a stowed position. The patient trolley is configured to dock adjacent the target modality such that the overhang area is capable of extending over at least a portion of the target modality. The patient trolley may be combined with a patient transfer device to facilitate transfer of a patient from the top surface of the patient trolley to the patient support surface of the target modality. Methods of docking the patient trolley adjacent a target modality and transferring a patient from the patient trolley to the target modality are also provided.

Abstract: A system may have a mobile device having at least two wheels and a distance measuring device configured to be removably attached to a frame of the mobile device, which can be a mobility assistance device, such as a walker and a wheelchair. The distance measuring device may have at least a sensing mechanism, an accumulator, and a display that are in communication with one another, with the sensing mechanism configured to monitor rotation of the at least one of the at least two wheels of the mobile device and the accumulator configured to determine the distance traveled by the mobile device based on this rotation and output the distance result on the display.

Abstract: A front wheel and a rear wheel are to be provided at a grounding frame. A body frame is mounted on the grounding frame and includes a mount at which a seat is to be provided. A relative position between the grounding frame and the body frame in a height direction of a wheelchair is changed via a height adjustment mechanism. The height adjustment mechanism includes an adjustment pole, a pole reception, and a holding portion. The adjustment pole extends along the height direction and is mounted on one of the body frame and the grounding frame. The pole reception is mounted on another of the body frame and the grounding frame and is engaged with the adjustment pole slidably in the height direction. The holding portion is to hold not to relatively move the adjustment pole with respect to the pole reception.

Abstract: A back support includes an anchor plate attachable to a back frame of a wheelchair and a spanning plate securable to the anchor plate in a range of vertical positions to adjust a height of the back support. The spanning plate is secured to the anchor plate by a fastener secured through an aperture in the anchor plate and attached to a laterally extending bar selectively engageable with the spanning plate in a plurality of discrete vertical positions.

Abstract: A caster wheel suspension assembly for a wheelchair or the like includes a housing with a clevis portion and a tubular portion; a fork member pivotably mounted in the clevis portion of the housing, the fork member having a pair of fork arms extending from the housing, each of the fork arms terminating in a lower end, the fork member having an upper portion formed as a clevis tang disposed in the clevis portion of the housing; a damping element in the tubular portion of the housing; and a compression adjustment element connected to the clevis pin and extending axially through the damping element. The compression adjustment element is configured to apply an adjustable compressive force to the damping element, and it is further configured to be moved axially within the tubular portion of the housing for adjustment of the compressive force applied to the damping element.

Abstract: Wheelchair devices and systems that have wheels with adjustable camber. The device has a bracket attached to a wheelchair and a receiver configured to couple to the axle of the wheel. The position of the receiver relative to the bracket can be adjusted by the user to alter the position of the axle relative to the bracket, thereby altering the camber in the rear wheel. A top portion of the rear wheel can remain in a vertical plane of travel regardless of the amount of camber in the wheel and a bottom portion of the rear wheel can remain in a horizontal plane.

Abstract: An adjustable bed includes a plank assembly, a support assembly, a frame and a power unit. The plank assembly includes a first waist plank and a second waist plank. The power unit is pivotally connected to the frame. The support assembly includes a waist-lifting unit that includes a first lifting element pivotally connected to a portion of the frame, a second lifting element pivotally connected to another portion of the frame, and a transmission unit operatively connected to the first and second lifting elements.

Abstract: Catheter monitor integration with patient support systems, such as patient beds, and with other healthcare communication systems including hand hygiene systems is provided. A patient bed that transmits bed data and catheter monitor data is disclosed. When catheter tubing is connected to a catheter monitor integrated into a patient bed, the bed automatically implements a falls prevention protocol. A countdown timer pertaining to removal of catheter tubing from a patient is displayed on one or more display devices. Monitoring for caregiver handwashing compliance in connection with use of a catheter monitor or a catheter kit is also provided.

Abstract: Systems, devices and methods are described for mounting medical equipment on IV poles, bed rails and other supporting structures in medical facilities including operating rooms and critical care sections. A system including a mounting hanger and corresponding equipment housing is disclosed that allows quick mounting and dismounting of equipment from a supporting structure. The novel structural design of mounting hanger including a symmetrical t-slot feature and a plunger lock allows a piece of equipment to be mounted on a supporting structure in multiple orientations as per the requirement which allows a user to optimize the placement of equipment in the medical environment.

Abstract: A patient-support status system includes a patient support apparatus adapted to support a patient thereon. A user interface is coupled to the patient support apparatus to move therewith and configured to receive a user input associated with a status of the patient. A location-detection system is configured to provide location data associated with a location of the patient support apparatus in a healthcare facility. A communication unit is coupled to the patient support apparatus and configured to communicate the status and the location data to a remote computer in response to receipt of the user input.