Abstract: The present invention provides a guidewire adjuster and a delivery-system control handle provided with the guidewire adjuster. The guidewire adjuster includes a support mechanism which has a lumen for a guidewire to extend therethrough; and a driving mechanism for driving the guidewire to move back and forth in the lumen. The guidewire adjuster is able to drive the guidewire to move with respect to a sheath of the delivery system. The support mechanism is connected to the control handle of the delivery system and forms a lumen for accommodating the guidewire. A proximal end of the sheath together with the stent can be driven to move upwardly, due to the relative movement between the guidewire and the sheath of the delivery system. Therefore, the position of the stent can be adjusted by advancing the guidewire forward when the stent has been deployed at a lower position than expected.

Abstract: The invention relates to an implantation device for implanting a vascular implant, which enables a vascular implant to be easily positioned and to be discharged in a slip-free manner.

Abstract: The present disclosure describes implantable medical devices comprising covers, such as a balloon cover. Such devices can comprise a first layer of a porous polymeric material, such as ePTFE, surrounded by layers of a porous polymeric material having an imbibed elastomer, such as polyurethane. The cover can be used to assist in deployment of an expandable implant, such as a stent-graft, within the body of the patient.

Abstract: The present disclosure describes methods of making a sleeve comprising a conical frustum having first and second end profiles and a lumen there through for covering and constraining an expandable device, and apparatuses, systems, and assemblies comprising an expandable device and a sleeve having a frustoconical shape when the expandable device is at least partially expanded. The present disclosure further describes methods for deploying an expandable device in a patient comprising releasing a releasable seam disposed on a sleeve and everting the sleeve while retracting it from the expandable device.

Abstract: The present disclosure relates generally to the field of medical devices. In particular, the present disclosure relates to delivery systems configured to position a distal portion of a medical device within a restricted anatomical area. In one example, a delivery system may include a flexible elongate member with an inner member within a lumen of the flexible elongate member. A stent may be constrained therebetween. The stent may be configured to move between a first configuration to a second deployed configuration when unconstrained from the flexible elongate member. When the stent moves from the first configuration to the second configuration, the inner member may change from a first length to a second, shorter length. Other embodiments are contemplated.

Abstract: A delivery system for endoluminal delivery of an expandable device comprising a catheter having a proximal end and an opposite distal end configured to support an expandable device, a primary sheath having a delivery position in which the primary sheath constrains the expandable device toward a collapsed configuration suitable for endoluminal delivery, and a handle including a first actuator that is actuatable to cause the expandable device to expand from the collapsed configuration, the handle further including a second actuator for operating one or more functions of the handle, wherein the second actuator is initially hidden to prevent actuation of the second actuator prior to the expandable device expanding and is configured to be revealed when the expandable device is expanded, the second actuator being actuatable once revealed.

Abstract: Systems, devices, and methods are provided for the delivery of an implant into the prostatic urethra. Embodiments of delivery systems can include a delivery device for insertion into the patient and a proximal control device for use in controlling release of the implant from the delivery device.

Abstract: A brace for treating a portion of a human body, the brace including a brace body including at least one fastener adapted for fastening the brace about the portion of the human body, and an aromatherapy heat-treatment pack removably attachable to the brace body, the aromatherapy heat-treatment pack containing at least one temperature maintaining component and at least one aromatherapeutic component, wherein the aromatherapy heat-treatment pack is adapted to maintain a temperature thereof for a predetermined treatment duration.

Abstract: Systems and methods are described for supporting an appendage or spine. In one embodiment, a support for a spine comprises a support body configured to align with a spinal column of a wearer further comprising a plurality of modular flexible support body segments configured to align with regions of the spinal column, a plurality of straps disposed along a longitudinal axis of the support body, and a support member disposed adjacent the support body to provide rigidity to the support body. The support member acts as a cantilever configured to distribute a corrective force along the length of the support body.

Abstract: The invention relates to an orthopedic device for supporting a back, especially a lower back, of a user, wherein the device comprises an upper body element 48, an upper leg element 4 and a first passive actuator 8, which is configured to apply a force to the upper leg element 4 and/or the upper body element 48 when an angle between the upper leg element 4 and the upper body element 48 is within a first predetermined angular range, wherein the device comprises at least a second passive actuator 10, which is configured to apply a force to the upper leg element 4 and/or the upper body element 48 when the angle is within a predetermined second angular range that is different to the first angular range.

Abstract: A splint and a method for operating a splint are disclosed. The splint includes a plurality of plates, at least one rope, and at least one fastening drive device. The plurality of plates include a first plate. The rope is in movable connection with the plurality of plates. The fastening drive device is on the first plate, and is connected to the rope and configured to drive the rope under control, so as to allow the rope to be tightened or loosened under drive of the fastening drive device to drive the plurality of plates to move relatively close to each other or relatively away from each other.

Abstract: A pediatric position holder for holding a child in a position is provided. The pediatric position holder includes a central panel extending longitudinally from a cranial portion to a caudal portion, arm flaps extending outwardly from opposing sides of the central panel, and leg flaps extending outwardly from opposing sides of the central panel. The arm flaps each include a proximal arm segment and a distal arm segment extending from the proximal arm segment. The leg flaps each include a proximal leg segment that defines one cutout and a distal leg segment extending from the proximal leg segment. The pediatric restraint is configurable between an initial, open configuration and a second, closed configuration in which the distal arm segments of the arm flaps overlap one another, and the distal leg segment of each of the leg flaps is positioned within the cutout of the respective leg flap.

Abstract: According to some embodiments of the invention, an anchoring system includes a sleeve having an inner surface defining a first lumen, a first annular sealing mechanism disposed at a proximal end of the sleeve, and a second annular sealing mechanism disposed at a distal end of the sleeve. The anchoring system further includes a pressure tube in fluid connection with an outer surface of the sleeve, a sheath in mechanical connection with the sleeve, the sheath forming a second lumen, the second lumen being in fluid connection with the first lumen, and open-cell foam disposed on the outer surface of the sleeve. Application of negative pressure to the pressure tube causes a seal to form between the first and second annular sealing mechanisms and an inner surface of a tissue cavity. Application of negative pressure to the pressure tube also creates a frictional force that resists displacement of the sleeve.

Abstract: Methods and apparatus for collecting fluids discharged from a urethra. An apparatus can include a housing with a rear and front portion a coupled together. A baseplate, inside the housing, includes an angled circumferential side surface adjacent to an inside surface of the housing, a main aperture, and a valve aperture extending through the baseplate. A discharge tube is coupled to the baseplate. An elastomeric tube extends from outside the housing to a termination point past the baseplate within the housing, the baseplate and the housing configured such that the collection tube is pinched and held in place between the baseplate angled circumferential side surface and an inside surface of the vented housing. One-way valves positioned in each valve aperture communicate air through the baseplate into the collection tube. A urethra tube, configured for collecting discharged urine, is positioned in a proximal end of the collection tube.

Abstract: An ostomy device includes a nonwoven element having a water-soluble component and a releasable material. When the ostomy device is applied to a user and stomal output contacts the distal surface of the nonwoven element, the water-soluble component dissolves and releases the releasable material from the nonwoven element to neutralize at least one of enzyme activity and pH of the stomal output.

Abstract: An oral treatment assembly providing a plurality of medical treatments of a patient that are non-invasive and in particular provides new methods for treating jaw related medical conditions of a patient through predetermined positioning and controlled or guided movement of a patient's mandible and therefore their mandibular condyles during use, wherein the assembly includes an upper and lower assembly each defining transition portions having a reverse cut angle that extends downward from the posterior forward to the anterior, and where each are configured to selectively engage to restrict the retrusion of the mandible relative to the maxilla and to position the mandible relative to the maxilla downward and in some embodiment slightly forward in a caregiver defined treatment position and having a caregiver defined treatment movement area thereabout. Since the reversed cut angle contains two vectors it also discourages involuntary dropping of the mandible relative to the maxilla.

Abstract: A pessary device has a support portion, a stem and a loop attached to the stem to facilitate manipulation and control of the pessary device. The loop portion is flexible and provides a hole for receipt of a finger of the person inserting or removing the pessary device. The loop portion preferably includes a taper and/or a dimpled end to facilitate the use of a finger or an applicator for insertion of the device deeper into the vagina.

Abstract: An electric heating pad for warming a patient includes a heated underbody support or heated mattress. The heated underbody support or mattress includes a heater assembly having a flexible sheet-like heating element, conductive bus bars attached at or near side edges of the heating element, and fabric side edge extensions attached to heating element side edges. The heated underbody support or mattress also includes a layer of polymeric foam positioned under the heater assembly and a shell, including at least two sheets of flexible material, covering at least a portion of the heater assembly and the layer of polymeric foam. When the heater assembly is wrapped around the top surface of the layer of polymeric foam, side edges of the heating element extend partially down the two side walls of the layer of polymeric foam and the conductive bus bars lie adjacent those two side walls.

Abstract: Invention is related to water used in combination with outdoor activity; which can include, recreation activities, therapeutic activities, exercise activities. Outdoor activity can be utilized by a user, or more than one user. Recreation activities can provide multiple user interface in a game format. Therapeutic activity can include, a smoking cessation modality, an improved immune system modality, a virus fighting modality which may include covid or related. Exercise activities can include, calorie burning, flexibility, strength, breathwork. Method can use a siphon water delivery. Invention can be used as a lawn watering device. Method can be supported with an app or other related technology, social media interface.

Abstract: A heat exchange module alone or part of a system including a control console. The HEM can include a channel enclosure assembly, a thermoelectric cooler (TEC) assembly and a heat transfer (cover) assembly. The enclosure assembly includes a channel for a heat-transfer liquid. The module can be constructed to provide for flexibility to better conform and fit on rounded and/or angular body parts and to efficiently transfer heat between the adjacent body part and the heat-transfer liquid via the TECs of the TEC assembly.

Abstract: An infusion pipe capable of achieving a flow rate higher or the same as that of a conventional product, and of easily joining to a cannula attached to an eyeball. The infusion pipe of the present invention is used in an ophthalmic operation with the infusion pipe joined to a cannula attached to an eyeball, and includes an insertion part to be inserted, at the time of joining to the cannula, inside a cannula piercing part, which is a part of the cannula for piercing the eyeball. A cross-section of the insertion part is an arc shape from which a part of a circle is cut out.

Abstract: An ophthalmic implant including an intraocular lens (IOL) and at least one drug delivery device. The IOL including an anterior side, a posterior side, a lens, and at least one haptic extending outwardly from the lens and including a first haptic extending from the lens at a first optic-haptic junction. The at least one drug delivery device including a first drug delivery device including a pad and a fixation portion extending from the pad. The pad including at least one therapeutic agent contained therein, an anterior surface, a posterior surface, and a sidewall extending around the pad and between the anterior surface and the posterior surface. The drug delivery device configured for attachment to the IOL via the fixation portion. In an assembled state of the implant, the first drug delivery device is attached to the IOL and the pad overlays the first optic-haptic junction.

Abstract: The present invention is a glaucoma implant device (1) comprising a connection portion (21) coupled to a mesh portion (11), whereby a first group of outlet ducts and second group of outlet ducts are configured such that the mesh portion (11) has a predefined hydraulic resistance threshold, and a stent portion (31) that dilates the Schlemm canal of an eye and directs aqueous humor to the connection portion (21), further directing aqueous humor into subconjunctival or suprachoroidal space.

Abstract: A method of treating a patient having an eye condition includes determining, during a pre-operative analysis of the patient, that the patient has a risk of developing glaucoma. The method further includes treating the patient with an excimer laser to prophylactically treat glaucoma based on the pre-operative analysis determination that the patient has the risk of developing glaucoma.

Abstract: A method is described of improving adhesion of an ocular implant to corneal tissue by forming an implant adhesive layer on the ocular implant, the implant adhesive layer having greater adhesive strength than a rest of the implant or by forming a corneal adhesive layer on a posterior surface of a posterior portion of the corneal tissue, the corneal adhesive layer having greater adhesive strength than a rest of the corneal tissue.

Abstract: A method implemented in an ophthalmic surgical laser system that employs a resonant scanner, scan line rotator, and XY- and Z-scanners, for forming a corneal flap in a patient's eye with improved bubble management during each step of the flap creation process. A pocket cut is formed first below bed level, followed by the bed connected to the pocket cut, then by a side cut extending from the bed to the anterior corneal surface. The pocket cut includes a pocket region located below the bed level and a ramp region connecting the pocket region to the bed. The bed is formed by a hinge cut and a first ring cut at lower laser energies, followed by a bed cut and then a second ring cut, which ensures that any location in the flap bed is cut twice to minimize tissue adhesion. The side cut is formed by multiple side-cut layers at different depths which are joined together. All cuts are formed by scanning a laser scan line generated by the resonant scanner.

Abstract: The present invention discloses a device suitable for delivery of a fluid composition to an eye, especially therapeutic compositions, comprising: a hollow needle with a bore having a proximal end and a distal end, said distal end configured to pass into a passage in a sclera of an eye, said bore configured to function as a conduit for a fluid from said proximal end to said distal end, and a solid separator having a distal tip, configured to move inside said bore of said hollow needle allowing said distal tip of said separator to protrude from said distal end of said needle.

Abstract: A glaucoma treatment eyeglass with visual stimulation includes the parts of visually stimulating screen, pressure control unit, electronic control and communication unit, information display, pressure control valve, eyeglass cavity pressure sensor, flexible sealing gasket, pressure control buttons, electronic control buttons, pressure pipes, external pressure control unit, actively stimulating light source, mini notice screen, mobile device and notice lamp, which patients with glaucoma eye disease may use during the day, increasing the ocular flow of blood by means of visual stimulus according to the condition and level of the disease, decreasing the neurodegenerative effects and ensuring pressure control.

Abstract: Safety glasses for a human user, with at least one lens which has an upper rim assignable to the user's forehead and a lower rim assignable to a user's cheek, with at least one nosepiece arranged at the at least one lens and with at least one protective lip to be supported on the user's face. The at least one protective lip only extends at the lower rim of the at least lens from the at least one nosepiece towards at least one of the outer lateral rims of the lens and, in extension of the lens, downwards from the lower rim of the lens to be supported on the user's cheek.

Abstract: Various systems are provided for an adjustable tilting head holder. In one example, a system comprises an adjustable tilting head holder for use with an imaging system the adjustable head holder comprising a head cradle, a tilt adjustment mechanism with a plurality of locking positions arranged below a first end of the head cradle, a table mount extending from a second end of the head cradle, and a tilt adjustment bar that extends from the table mount through the tilt adjustment mechanism, wherein the first end and the second end of the head cradle are located at opposite ends of the head cradle.

Abstract: A support platform for body treatment is provided and includes a supporting frame, a resilient pad, a guide passageway, a cushion and a control assembly. The resilient pad is secured to the supporting frame and includes an upper surface positioned opposite the supporting frame. The guide passageway extends from the upper surface and through the resilient pad toward the supporting frame. The cushion includes a lower surface side and is connected to control assembly so that it vertically positions the lower surface side along the guide passageway.

Abstract: A customizable memorabilia cover has front and back substantially rectangular leafboard members coupled to a spine member. Elastic bands may be coupled one each at the distal and proximal ends of the elastic bands substantially to the outer corners of the rectangular leafboard members. The elastic bands are disposed acutely from the edges of the rectangular leafboard members and designed to receive the corners of a book cover of a book therethrough, the book contained within the front and back leafboard members substantially abutted by the spine member. At least one groove member of the front leafboard member has a closed base and closed side members. A substantially transparent cover member is contiguously coupled to a top portion of the side members to define an ash container assembly. An alternative embodiment includes a covering or enclosing member that holds an electronic handheld device removably coupled to the back leafboard member.

Abstract: A wheelchair armrest storage system may include a housing for a wheelchair, where: the housing includes a proximal portion, a distal portion, a first lateral side, and a second lateral side, the housing extends longitudinally between the proximal portion and the distal portion, and at least one cover receiving cavity is defined in each of the first lateral side and the second lateral side. The wheelchair armrest storage system may further include a storage area defined within the housing, and a cover configured to translate within each of the at least one cover receiving cavity defined in each of the first lateral side and the second lateral side.

Abstract: Drifting karts in accordance with embodiments of the invention are described that include a front wheel drive train and rear caster wheels that can be dynamically engaged to induce and control drift during a turn. One embodiment of the invention includes a chassis to which a steering column is mounted, where the steering column includes at least one front steerable wheel configured to be driven by an electric motor, a battery housing mounted to the chassis, where the battery housing contains a controller and at least one battery, wiring configured to provide power from the at least one battery to the electric motor, two caster wheels mounted to the chassis, where each caster wheel is configured to rotate around a rotational axis and swivel around a swivel axis, and a hand lever configured to dynamically engage the caster wheels to induce and control drift during a turn.

Abstract: Embodiments of a wheelchair and suspension system are provided. The suspension includes a drive assembly that is pivotably connected to a base frame at multiple locations. In one embodiment, the connection is via intermediary pivoting links or arms. Embodiments of the links or arms including rigid links, resilient links, elastic links, shocks, springs, gas cylinders and lockable gas cylinders (or combinations of the foregoing). The drive assembly can, via the pivot connections, pivot to accommodate and traverse variations and obstacles on ground surfaces.

Abstract: According to certain arrangements, a conditioner mat for use with a bed assembly includes an upper layer comprising a plurality of openings, a lower layer being substantially fluid impermeable, at least one interior chamber defined by the upper layer and the lower layer and a spacer material positioned within the interior chamber. In one embodiment, the spacer material is configured to maintain a shape of the interior chamber and to help with the passage of fluids within a portion of interior chamber. The conditioner mat can be configured to releasably secure to a top of a bed assembly.

Abstract: A cervical traction assembly for use with a patient support apparatus includes an adjustment carriage track member including a connecting bracket assembly that releasably connects to a mount support member of the patient support apparatus. The adjustment track member includes a track body including a pair of opposing sidewalls that are spaced-apart from each other to define an elongated channel therebetween. Each sidewall includes a guide track that extends along a length of the respective sidewall. A rope angle adjustment carriage is located within the channel. The rope angle adjustment carriage includes a first track engagement member that is received by one of the guide tracks of one of the sidewalls and a second track engagement member that is received by another of the guide tracks of another of the sidewalls. The first track engagement member has a locked configuration that inhibits movement of the rope angle adjustment carriage.

Abstract: A knee rehabilitation device may include a left post and a right post, an upper transverse post and a lower transverse post. The transverse posts may extend from the left post to the right post and may include foam pads that are configured to rest against opposing sides of the user's legs. The left and right posts may be angled to facilitate handling of the device. The transverse posts may be attached to the left and right posts by clamps that allow the transverse posts to slide along the height of the left and right posts.

Abstract: A rehabilitation exercise device for upper and lower limbs is provided. The rehabilitation exercise device includes: a first support supporting a user's hand or foot; a second support supporting a user's forearm or calf; a pair of first hinges rotatably connecting the first support and the second support to each other; a third support supporting a user's upper arm or thigh; a pair of second hinges rotatably connecting the second support and the third support to each other; and a distance adjustment part configured to adjust a distance between the first support and the third support by adjusting length of the second support.

Abstract: A heel clamp, or posterior component, for an article of footwear is provided. The heel clamp may comprise a posterior component height value measuring a height value from a lowest point under the heel of the foot on an upper facing surface to a top of the posterior component. A lateral component and a medial component of the heel clamp may include a predetermined height value or an extension height value. The lateral component may be extending into or through an area in-between a lateral malleolus bone of the foot and an Achilles tendon of the foot, the medial component may be extending into or through an area in-between a medial malleolus bone of the foot and the Achilles tendon of the foot, and the intermediate component may be extending to an area of an end of a top of a calcaneus bone of the foot.

Abstract: A massage device for a person's appendage includes a plurality of enclosures each including an outer surface and a hollow interior space having a control circuit, a power source such as a rechargeable battery, a vibration mechanism, and preferably at least one motor and a gear arrangement. Each enclosure includes at least one roller driven by the gear arrangement and the at least one motor. A plurality of connectors are each fixed between two adjacent enclosures to form a ring with the enclosures and the connectors. The connectors are adapted to contract or expand such that with the person's appendage fitted through the ring, the connectors are retracted until the rollers each contact the person's appendage to move the device along or about the person's appendage while the vibration mechanism massages the person's appendage.

Abstract: The method of treating a patient addicted to pain medication or opioids has the step administering acoustic shock waves or pressure pulses to the patient. A second embodiment includes a treatment to reduce a patient's pain caused by a medical condition and/or medical procedure to reduce or eliminate the taking of addictive pain medication. The treatment has the step of administering acoustic shock waves or pressure pulses directed to an area near a source of the pain or to one or more reflexology zones or to one or more reflexology zones and to an area near the source of the pain or both to treat the medical condition or prior to the medical procedure or during the medical procedure or after the medical procedure or any combination thereof.

Abstract: A compression garment apparatus for a body part of an human and/or animal having a flexible backing, attaching means, a segmented flex frame, and a shape memory alloy on the segmented flex frame. The shape memory alloy can be connected to two terminals on the frame forming a circuit. A controller can be connected to the terminals applying current to the shape memory alloy at defined intervals providing intermittent, sequenced, or continuous compression therapy.

Abstract: An exosuit includes a first structure including a series of link elements joined together by joints. The series of link elements extends along a length of the first structure. The joints are configured to flex such that, when the exosuit is worn by a user, the first structure at least partially conforms to a shape of the user's anatomy at a first side of the first structure that extends along the length. The joints restrict flexing that would deform a second side of the first structure extending along the length of the first structure. The exosuit includes a second structure and an actuator coupled to the first structure and the second structure. The actuator causes movement of the first structure relative to the second structure. The exosuit includes an attachment portion to attach the exosuit to the user with the first side of the first structure facing toward the user.

Abstract: When a frontmost white line of a crosswalk cannot be detected due to an obstacle existing on the crosswalk, an edge position of the obstacle closer to a pedestrian in an image acquired by a camera is set as the frontmost white line of the crosswalk. As a result, a vibration generation device vibrates in a pattern that urges the pedestrian to stop at the time when the pedestrian reaches a position before the edge position of the obstacle closer to the pedestrian, so that a stop notification for walking can be appropriately performed to the pedestrian even when the obstacle exists on the crosswalk.

Abstract: Systems and methods are provided for ultrasound imaging with real-time feedback for cardiopulmonary resuscitation (CPR) compressions. Ultrasound images generated based on received echo ultrasound signals during cardiopulmonary resuscitation (CPR) of a patient may be processed, and based on the processing of the ultrasound images, real-time information relating to the cardiopulmonary resuscitation (CPR) may be determined. Feedback for assisting in conducting the cardiopulmonary resuscitation (CPR) may be generated based on the information. The feedback may include information and/or indications relating to compressions applied during the cardiopulmonary resuscitation (CPR). The feedback may be configured for outputting during displaying of the generated ultrasound images.

Abstract: A massage system includes a massage head configured to contact a treatment region of a patient during a massage treatment procedure, a body having a handle, a connector having a first end and a second end, wherein the first end is releasable secured to the body and the second end is coupled to the massage head, a motor positioned within the body and configured to drive movement of the massage head relative to the body, and a platform configured to be placed against the patient during a massage treatment procedure. The platform defines an opening. The platform is positioned so that the massage head extends at least partially through the opening during movement of the massage head relative to the body, and the platform surrounds the massage head in at least one dimension during movement of the massage head relative to the body.

Abstract: A container unit may be used to facilitate administrations of multiple medicinal fluids to a patient. A container unit may include a first container, a second container, and a carrier which holds the first container and the second container stationary relative to each other. The carrier may include a lip configured to engage a pooling device to secure the container unit to the pooling device. The carrier may also include a slot configured to engage an insert on the pooling device to guide the container unit as the container unit is secured to the pooling device. The carrier may also include a first portion and second portion with different shapes that are complementary to a shape of a port on the pooling device. The carrier may also include an extension which extends in a direction away from one of the first container to a level at least even with a stopper disposed in the first container.

Abstract: A syringe adapter includes a housing having a first end and a second end with the first end configured to be secured to a first container, a cannula having a first end and a second end with the second end positioned within the housing, and a collet having a first end and a second end with at least a portion of the collet received within the housing. The collet includes a body defining a passageway, a seal member received by the passageway, and an arcuate, resilient locking member connected to the body of the collet. The collet is movable from a first position where the locking member is open to receive a mating connector to a second position where radially outward movement of the locking member is restricted.

Abstract: Fluid transfer couplings or connectors including dual function press-in bottle adaptors supporting different syringe types, connectors having a universal port for supporting different syringe types, transfer couplings compatible for use with different syringe types. Other caps and closures incorporating couplings for fluid transfer with different syringe types is also disclosed.