Abstract: Stand-alone interbody fusion devices for engagement between adjacent vertebrae. The stand-alone interbody fusion devices may include frames and one or more endplates coupled to the frame. The frame may be configured and designed to provide the apertures which are designed to retain bone fasteners, such as screws or anchors, and secure the implant to the adjacent vertebrae.

Abstract: A device includes an upper endplate having an engagement surface, an inner surface and first projections extending from the inner surface. The first projections each include a first inclined surface. A lower endplate includes an engagement surface, an inner surface and second projections extending from the inner surface. The second projections each include a second inclined surface. A wedge is positioned between the endplates. The wedge includes first mating parts that engage the first inclined surfaces and second mating parts that engage the second inclined surfaces. The wedge is movable relative to the endplates to move the device between a first configuration having a first height between the engagement surfaces and a second configuration having an increased second height between the engagement surfaces. Methods of use are disclosed.

Abstract: The invention provides an inter-body spacer in the form of a vertebral body replacement. The spacer comprises a connector having, axially aligned, a socket and threaded socket. A threaded screw is receivable in the threaded socket of the connector at one side of the screw and an endplate receiving head is provided on the other end of the screw for receiving an endplate perpendicular to the axis. The spacer further comprises a cylindrical extension with one end rotatably receivable in the socket of the connector and an endplate receiving head on the other end of the extension for receiving an endplate perpendicular to the axis. A locating formation is provided on each endplate receiving head for locating the endplate at a specific angle about the axis. The spacer further comprises a selection of one or more end plates receivable on the endplate receiving head with the tissue engaging surface of the endplates being transverse to the axis of the spacer at differing angles.

Abstract: The disclosure provides apparatus and methods of use pertaining to a bidirectional biomechanical prosthetic finger assembly. In one embodiment, the assembly includes an eccentric metacarpophalangeal (MCP) pivot configured for swivelable attachment to a hand of a user, a distal coupler, and an articulation assembly rotatively coupled therebetween. A ring configured to receive a user's residual finger is disposed upon the articulation assembly, and may be adjusted to a target location based on a length of the residual finger. The articulation assembly is configured to utilize vertical movements of the residual finger within the ring to articulate the distal coupler within a plane parallel to an x-z plane, and the MCP pivot is configured to utilize lateral movements of the residual finger within the ring to articulate the distal coupler within a plane parallel to an x-y plane. Other embodiments are also disclosed.

Abstract: Embodiments of the present disclosure provide techniques and configurations for a robotic apparatus with an actuator formed by multiple fibers, in accordance with some embodiments. In some instances, the robotic apparatus may include an actuator to cause a motion of a component of a robot. The actuator may include at least one fiber that may comprise a conductive pattern. The conductive pattern may be embedded in a sheet of elastic material formed into a layered structure. The fiber may expand or contract in response to an application of a voltage signal to the conductive pattern, to cause the motion of the component of the robot. The fiber may comprise multiple fibers combined in a bundle, to form the actuator. The layered structure may comprise a roll-like shape that may be free of hollow spaces. In embodiments, the robot may comprise the robotic apparatus. Other embodiments may be described and/or claimed.

Abstract: An apparatus and manufacturing method for a reinforced fill-compositing prosthetic device. A prosthetic device is manufactured according to an additive manufacturing method. The prosthetic device is manufactured with a multitude of internal channels running in one or more linear or angular paths relative to a calculated sheer force direction, which may follow the contours of the prosthetic device. Channels defining an internal structure of a socket wall are open on at least one end of the prosthetic device. One or more structural inserts comprising a strength tested tensile strength material, such as carbon fiber, are inserted into the channels and bonded into place.

Abstract: An additive manufacturing method and apparatus for interchangeable local interface support geometry and materials in lower limb prosthetic sockets. An interchangeable local interface prosthetic socket is configured to enable a user of the socket to configure variable support, pressure, and comfort characteristics of lower limb prosthetic sockets by selectively replacing an interface panel and/or distal cup with an alternative interface panel and/or distal cup being configured to have different physical characteristics.

Abstract: The present invention teach an overlapping covered stents with uncovered segments capable of effectively diverting blood flow away from an aneurysm or fistula while allowing blood to flow to its normal vascular territory of healthy tissue distal to the targeted treatment area and still resulting in blood stasis and thrombus formation inside the aneurysm or fistula.

Abstract: A stent with a one-way sock valve comprises a stent portion and a one-way valve portion. The one-way valve portion comprises a heal portion. The heal portion prevents solids and liquids from entering an opening in the one-way valve portion. Solids and liquids enter the one-way sock valve in a first direction through the stent portion and exit an opening transversely to the longitudinal axis of the stent portion. The sock valve folds, closing the sock valve to any reverse flow in a second direction opposite of the first direction.

Abstract: A system for internal iliac preservation includes a catheter having a distal catheter portion and a proximal catheter portion; a first guidewire having a proximal portion extending from the proximal catheter portion, a distal portion and a medial portion disposed between the proximal portion and the distal portion; a first outer sheath slidably disposed over distal catheter portion; and an integrated second delivery system disposed within the outer sheath at the distal catheter portion. The integrated second delivery system includes a second guidewire; an expandable stent-graft disposed over a lumen of the second guidewire, and a slidable connector slidably disposed over the medial portion of the first guidewire, where the second guidewire is slidably engaged with the slidable connection to permit movement of the integrated second delivery system along the first guidewire when the first outer sheath is retracted from distal catheter portion.

Abstract: A catheter configured to carry one or more stents and having an inflatable balloon for expanding a stent surrounding the balloon. The catheter is characterized in having a positioner for moving the one or more stents relative to the balloon from a first position in which the stent does not surround the balloon to a second position in which the stent surrounds the balloon. Also disclosed is a method for deploying a stent at a desired location in the vascular system.

Abstract: In one aspect of the invention, a preloaded stent graft delivery device includes a guidewire catheter having a proximal end, a distal end, and a guide wire lumen therethrough; a nose cone dilator at the proximal end of the guide wire catheter, the nose cone dilator comprising a distal end and a capsule on the distal end of the nose cone dilator; a handle assembly at the distal end of the guidewire catheter, the handle assembly comprising a first section and a second section releasably connected to the handle assembly and in communication with the capsule on the distal end of the nose cone dilator; a ratchet assembly disposed within an interior surface of the first section of the handle assembly; a pusher catheter extending from the handle assembly towards the nose cone dilator; and a sheath disposed coaxially over the pusher catheter.

Abstract: A device for treating obesity of a patient, the device comprising: at least one operable stretching device implantable in the patient and adapted to stretch a portion of the patient's stomach wall, and an implantable control unit for automatically controlling the operable stretching device, when the control unit and stretching device are implanted, to stretch the stomach wall portion in connection with the patient eating such that satiety is created.

Abstract: The invention relates to a pivoting-limitable biaxial joint, especially for a joint orthosis for supporting and variably limiting the joint flexion. The invention provides an improvement of known joint orthoses. A limiting wedge (300) can be inserted into the joint housing (200) in the axial direction.

Abstract: Systems, methods, and apparatus provide an artificial knee. Such artificial knees may include a thigh link configured to move in unison with a thigh of the person, a shank link configured to be rotatably coupled to the thigh link, and a compression spring rotatably coupled to the thigh link at a first end and coupled to the shank link at a second end. The compression spring is configured to provide an extension torque between the thigh link and the shank link during a first range of motion of the thigh link and the shank link relative to each other. The compression spring is configured to provide a flexion torque between the thigh link and the shank link during a second range of motion of the thigh link and the shank link relative to each other.

Abstract: The proposed method is an innovative approach to correcting orthopedic deformities. It involves gradual manual mobilization of contracture soft tissues and diminutive foot joints by a physiotherapist, followed by mechanical reinforcement of the resulting effect by an orthosis which depresses and push the Ist, IVth and Vth metatarsal bones while elevating or actually blocking the fall the immobile IInd and IIIrd metatarsal bones according to the “three forces” rule. Correction transverse arch foot runs simultaneously with the correction of hallux valgus (if necessary). The propose method comprises sequentially applied passive redression (manual treatment), and a follow-up with the use of a specially designed orthosis (mechanical treatment). The method is suitable for patients undergoing preparation for corrective HV surgery and for post-operative HV. Method can be used preventively e.g. in women who frequently wear high-heel shoes and in for those who need to remain standing for prolonged periods of time.

Abstract: A cervical collar dimensioned to fit a human patient's neck is constructed primarily of foam. It has a foam body with a main top surface and a bifurcated (“M”-shaped) top portion which extends significantly upwardly from the main top surface so as to allow the midline of the occiput to float, thereby minimizing ulceration-causing pressure. The foam body may have a density of at least about 1.4 lbs/ft3, and a mound like bottom projection may extend from a main bottom surface thereof. The foam body may have slits formed in it, and a rigidity-enhancing element is inserted into a slit. By inserting different rigidity-enhancing elements the rigidity of the foam collar may be adjusted. The rigidity-enhancing element may have a C-shape with a hinge spring between two rigid portions.

Abstract: An adjustable compression device (10) comprising an elongate rigid band (12) provided to extend around a portion of the circumference of a penis (16). The band (12) includes first and second side portions (18, 20) connecting by an intermediate portion (22). An engagement member (14) is secured between the first and second side portions (18, 20) such that the engagement member (14) is rotatable about a rotational axis (24) extending between the side portions (18, 20). The engagement member (14) is off-centred relative to said rotational axis (24) such that an area defined between the engagement member (14) and the band (12) can be increased or decreased by rotation of the engagement member (14) thereby adjusting pressure applied to the penis (16).

Abstract: The invention is generally a dental appliance that, in exemplary embodiments, includes a mouthpiece equipped with a tongue-securing mechanism. The dental appliance helps keep a user's airway unobstructed by securing a tip portion of the tongue slightly forward relative to the mouth so that the tongue is held from falling back into the throat. This invention helps alleviate problems including severe snoring and sleep apnea, which are typically caused by the tongue obstructing the airway at the throat, thus impeding respiration during sleep or when unconscious. In an exemplary embodiment, the dental appliance comprises a mouthpiece which is configured to circumscribe a tongue retaining mechanism, or tongue sleeve, that secures a user's tongue in place.

Abstract: Described herein is a vaginal ring applicator comprising a barrel comprising a polymer and at least one friction reducing agent, wherein the barrel is a flattened cylinder having two slightly curved and opposing sides connected by two arcs, wherein the barrel extends between an insertion end and a plunger end; and a plunger extending between distal and proximal ends, wherein the distal end of the plunger engages the plunger end of the barrel and wherein the plunger fits telescopically within the barrel.

Abstract: A portable blower includes a tube that may be adjusted to place air flow at a desired location and in a desired orientation, for example, on a feverish location, a damp location, and/or a wound on an individual's body while the individual convalesces. A method of using such a portable blower includes placing a housing of the portable blower at a location (e.g., outside of bedsheets or blankets, etc.) where the portable blower can take in air, and positioning a distal end of a hose whose proximal end has been coupled to an output of the portable blower at a location and in an orientation where ventilation will be provided to a desired location on an individual's body (e.g., a location covered by a gown, clothing, and/or bedsheets or blankets, etc.). The hose may retain the configuration into which it is adjusted.

Abstract: A self-contained modular cooling device vessel having at least one cooling module defined by a pod, a frame, and an integrated connecting means. An insulating substance is contained within at least part of the pod in order to cool a user at temperatures higher than the predetermined temperature of the insulating substance when placing the cooling module proximal to the user's body. The cooling device can include an enclosure that is wearable by the user.

Abstract: Disclosed herein is an incision part formed in a cornea to remove a lenticule cut in the course of vision correction surgery, the vision correction surgery for correcting abnormal refraction being performed by drawing a dense spiral toward the center of the cornea or outward from the center of the cornea while three-dimensionally changing the focal point of a laser beam to form a flap surface and a lenticular surface each having a continuous spiral incision line in a corneal stroma such that the flap surface and the lenticular surface are spaced apart from each other, making the outer circumference of the lenticular surface intersect the outer circumference of the flap surface inside the outer circumference of the flap surface to cut a three-dimensional lenticule from the corneal stroma, and removing the lenticule out of the cornea through an incision part formed in the cornea, wherein the incision part includes an incision entrance formed in the surface of the cornea adjacent to the outer circumference of th

Abstract: The present invention relates to an ophthalmic treatment apparatus and a method for controlling same. The ophthalmic treatment apparatus according to the present invention comprises: an image unit for generating an image of the retina area of an eyeball in a horizontal direction with respect to the plane of the focal spot of a therapeutic beam directed by a beam delivery unit; a pattern unit for providing a grid pattern to the retina area so as to correspond to the curvature of the retina area generated by the image unit; and a control unit for controlling the operation of a beam generation unit and the beam delivery unit to radiate the therapeutic beam to the intersection points of the grid pattern on the basis of the grid pattern provided by the pattern unit.

Abstract: An injector apparatus comprises an elongate structure having one or more openings positionable near a penetrable barrier of an implantable device so as to receive fluid of the implantable device. The apparatus comprises a needle and a sheath extending over at least a portion of the needle. The elongate structure may comprise a distal tip to penetrate tissue and the penetrable barrier, and a distal opening near the tip to release therapeutic fluid into the implantable chamber. In many embodiments the distal tip, the distal opening, and the plurality of openings are separated from a stop that engages a tissue of the patient and limit penetration depth such that the distal opening and the plurality of openings are located along an axis of the implantable device to increase an efficiency of the exchange.

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

Abstract: A system (10, 200) and corresponding method for introducing a drug delivery device (18, 218) through at least part of a biological barrier starts with the drug delivery device (18, 218) deployed within a channel of a hollow needle (12, 212). The hollow needle is inserted into the biological barrier and the drug delivery device is pushed forward by a suitable plunger. The drug delivery device is preferably anchored to the biological barrier through a radially expanding retention arrangement (36, 36?, 36a), and is preferably filled with a liquid drug after deployment via a filling needle (24, 222) extending within the channel of the hollow needle (12, 212).

Abstract: A vitreous body cutter that allows wide movement of an opening position at the end part of a pipe even when the pipe is thin and that allows suction of vitreous bodies etc. in a wide range. The vitreous body cutter includes: a pipe having an opening on the side of an end part; a cutter, which slides along the inner surface of the pipe; a power output section, which is connected to the pipe and slides the cutter; and an outer case, through which the pipe passes, and which includes the power output section inside; and further includes a joint for connecting the outer case to a cannula attached to an eyeball. The protrusion length of the pipe from the outer case can be changed.

Abstract: A handheld reciprocating surgical tool may contain an inertial damper to counteract the momentum of a diaphragm assembly of the reciprocating surgical tool. A momentum of the inertial damper may be tuned such that the momentum of the inertial damper is comparable in magnitude and opposite in direction to a momentum of the diaphragm assembly. The diaphragm assembly may include a cutting tool. The combined momentum of a diaphragm assembly and the inertial damper may result in a reduced net momentum, which may reduce vibration of the reciprocating surgical tool haptically experienced by a surgeon, thereby improving surgeon comfort.

Abstract: Embodiments of the claimed invention are directed to the treatment of glaucoma (or conditions of elevated intraocular pressure) using a novel ab interno trabeculotomy procedure that uses a flexible device. At least one advantage of the present method is that it does not require a conjunctival or scleral incision, which in turn improves patient recovery time and healing.

Abstract: An example multi-fiber, multi-spot laser probe comprises a plurality of fibers extending from a proximal end of the laser probe to at least near a distal end of the laser probe, where the proximal end of the laser probe is configured to be coupled to a laser source via an adapter interface, and a cannula having a distal end and surrounding the plurality of fibers along at least a portion of the laser probe at or near the distal end of the laser probe, where a distal end of each of the plurality of fibers is angle-polished so that the distal end of each fiber is angled relative to a longitudinal axis of the cannula and relative to a plane perpendicular to the longitudinal axis of the cannula. Additional embodiments employ lensed fibers, a distal window, ball lens, lens array, or faceted wedge.

Abstract: Multi-fiber laser probes utilize relative motion of fibers and other laser probe elements to preserve small-gauge compatibility while providing for multi-spot beam deliver, or to provide for the selectively delivery of single-spot or multi-spot beam patterns. An example probe includes fibers having distal ends that are movable as a group onto a distal ramp element affixed to a distal end of a cannula, so that the distal ends of the fibers can be moved between a retracted position, in which the distal ends of the fibers are within the cannula or ramp element, and an extended position, in which distal ends of the fibers are guided by grooves or channels of the ramp so as to extend at least partially through external openings in the distal end of the laser probe and so as to be pointed angularly away from a longitudinal axis of the cannula.

Abstract: A tool communication adapter system is provided. One exemplary system described herein includes a tool communication adapter having an adapter body including first and second mechanical attachment ends, a first electrical connector proximate the first mechanical attachment end and a second electrical connector proximate the second mechanical attachment end, a first supply channel having an opening extending through the body between the first and second mechanical attachment ends, and including a first supply channel connector at the first attachment end and a second supply channel connector at the second mechanical attachment end, and a control unit in communication with the first and second electrical connectors. The control unit is configured to provide a filter command signal to a protective filter in response to a signal received at the first electrical connector. An exemplary tool communication adapter thus allows communication between a tool and personal protective equipment.

Abstract: An absorbent composite includes a porous base layer, a core layer, and a superabsorbent laminate layer. The core layer has a fluff pulp layer and superabsorbent polymer particles. The core layer is disposed on the base layer. The superabsorbent laminate layer is disposed on the core layer. The base layer, the core layer, and the superabsorbent laminate layer are compressed together and embossed under heat and pressure to form a plurality of embossed depressions. The embossed depressions are arranged across a major surface area of the superabsorbent laminate layer. The embossed depressions extend through the composite from the superabsorbent laminate layer and into the core layer and the base layer. A thin, soft, and pliable absorbent composite suitable for a variety of applications including wound care is thereby provided.

Abstract: Disclosed herein are antimicrobial elastic support bandages including a plurality of warp threads extending along at least a portion of the length thereof and including non-antimicrobial warp regions and antimicrobial warp regions arranged in an alternating fashion across the width thereof, wherein (a) a non-antimicrobial warp region comprises an elastic material that is stretchable in the direction of the length, (b) an antimicrobial warp region comprises (i) a flexible fiber coupled to an antimicrobial metal, and (ii) an elastic material that is stretchable in the direction of the length, wherein the flexible fiber is coupled to the elastic material, and (c) at least a portion of the warp threads are separated by about 3 microns to about 20 microns; and further including a plurality of weft threads extending across at least a portion of the width and comprising a biocompatible material, wherein at least some of the weft threads are separated by about 3 microns to about 20 microns, wherein at least a portion

Abstract: Provided is a medical dressing patch which is used to simultaneously protect and treat an injury to a skin such as burns, wounds, and traumas, and a method and an apparatus for manufacturing the medical dressing patch, and more particularly, to a medical dressing patch including: a release paper; and an adhesive sheet which is fixed to an upper portion of the release paper and attached to a skin, in which the release paper includes a fixing release paper, and a separation release paper which is fixed to the fixing release paper through a cut-out portion and a connecting portion formed on the fixing release paper, and positioned such that a predetermined region of the separation release paper overlaps a lower surface of the adhesive sheet so that the separation release paper is separated together with the adhesive sheet when the adhesive sheet is separated from the fixing release paper, and a method and an apparatus for manufacturing the medical dressing patch.

Abstract: A method and apparatus are disclosed for dressing a wound. The apparatus comprises an absorbent layer for absorbing wound exudate, a liquid impermeable, gas permeable filter layer over the absorbent layer, a cover layer comprising at least one orifice and a first liquid and gas permeable transmission layer underlying the absorbent layer. The transmission layer is in fluid communication with the filter layer.

Abstract: A method for establishing a compression level to a human limb or body part by a compression garment is shown, the garment consisting of or including a bandage having at least one closing part, which closing part is securable on the garment in a position wherein the bandage is fully or partly wrapped around said limb or body part to establish said pressure level, the method including a first step of wrapping the bandage around the limb or body part and provisionally securing it in a first position that holds the compression garment on the limb or body part without applying a compression level to said limb or body part; a second step of applying a tab with an adhesive or attaching mechanism to the garment, the tab abutting the terminal edge of the closing part; a third step of releasing the closing part from its provisionally secured position and wrapping the bandage part further around the limb or body part, using the length of the tab as a marking for a safe compression level range; and a fourth step of secur

Abstract: Disclosed are systems, methods, and devices related to a cast portal. The cast portal can be for enabling selective access through a medical cast to a body part covered by the medical cast. One illustrative cast portal includes an interior portion that extends through an entire longitudinal length of the cast portal. The illustrative cast portal can also include an outer housing that defines the bounds of the interior portion. The outer housing can include a top end configured to be positioned distal to the body part covered by the medical cast. The outer housing can also include a bottom end configured to be positioned proximate to the body part covered by the medical cast. The illustrative cast portal can also include a protrusion extending radially outwardly from the outer housing and configured to mechanically couple with the medical cast for attaching the device to the medical cast.

Abstract: An absorbent article may include an inner elasticised chassis. An opening may be formed through the inner elasticised chassis. The absorbent article may include an outer elasticised chassis, and an absorbent member located between the inner elasticised chassis and the outer elasticised chassis. The inner elasticised chassis may include sets of elastic strands surrounding the absorbent member. The opening may be located in a space between the sets of elastic strands.

Abstract: An individual package for an absorbent article is provided with the absorbent article and a wrapping body containing the absorbent article. The absorbent article has a main body extending in a longitudinal direction and a pair of flaps extending from the main body in opposite directions along the longitudinal direction. Each of the main body and the pair of flaps has a fixing section and the main body and the pair of flaps are fixed to the same face of the wrapping body with the fixing sections interposed therebetween. The wrapping body is provided with a pair of bonding regions bonding the wrapping body, the bonding regions being located outward in the widthwise direction and each having a bonding section and a non-bonding section. The fixing sections of the pair of flaps and the non-bonding sections overlap in the widthwise direction.

Abstract: A pant-type absorbent article has a longitudinal direction, a transverse direction, an inner surface facing the user during use, an outer surface facing away from the user during use. The article includes: a first body portion, a second body portion and an intermediate crotch portion provided with two leg openings. Outer longitudinal edge portions of the first body portion are adapted to be interconnected to outer longitudinal edge portions of the second body portion by first and second longitudinal refastenable side seam configurations. Each one of the refastenable side seam configurations includes a fastening component bonded to an outer longitudinal edge portion of the first body portion and a mating fastening component bonded to a corresponding outer longitudinal edge portion of the second body portion. Moreover, each one of the fastening components and the mating fastening components includes a first mechanical connector structure and a second mechanical connector structure.

Abstract: A body position fixing apparatus includes an indicating rod and a rotation mechanism that supports the indicating rod to make the indicating rod rotatable at a discretionary angle relative to each of the placement surface and a fixed reference plane including the first pressing surface, the second pressing surface, and the third pressing surface.

Abstract: A robotic operating table according to one or more embodiments may include: a patient placement table; a robotic arm comprising a plurality of joints, and having a first end supported on a base and a second end supporting the table; and an operation device comprising a preset position registration setting unit that registers an anesthetization position, a surgical operation position, and an imaging position and sets one of the registered anesthetization, surgical operation, and imaging positions as a movement destination of the table, and a move-operation receiving unit that receives, from a user, a move operation to move the table. When the move-operation receiving unit is operated while one of the registered anesthetization, surgical operation, and imaging positions is set as the movement destination of the table, the robotic arm may move the table to the set one of the registered anesthetization, surgical operation, and imaging positions.

Abstract: A robotic operating table according to one or more embodiments may include: a table on which to place a patient; a robotic arm including a plurality of joints, and including a first end supported on a base fixed to a floor, and a second end supporting the table; an operation device including: a move operation receiving unit that receives, from a user, a move operation to move the table, and a register operation receiving unit that receives, from a user, a register operation to register a position of a movement destination of the table and a movement-destination set operation; a memory; and a controller that causes the robotic arm to move the table based on the move operation received by the move operation receiving unit.

Abstract: A robotic operating table may include: a table on which to place a patient; and a robotic arm including a plurality of joints, and having a first end supported on a base fixed to a floor, and a second end supporting the table; and an operation device including: a mode-set operation receiving unit that receives a set operation to set a rotation mode for rotating the table; a move operation receiving unit that receives a move operation to move the table; and a display. When the mode-set operation receiving unit receives the set operation to set the rotation mode, the display may display setting information for setting a rotation center position of the table. When the move operation receiving unit receives the move operation in a state where the rotation center position is set, the robotic arm may rotate the table about a rotation axis at the rotation center position.

Abstract: An operation device according to one or more embodiments may include: a display; a move operation receiving unit that receives, from a user, a move operation to move a table on which a patient can be placed of an operating table; and an operation controller. In a condition in which the table is put in a tilted posture in accordance with the move operation, the operation controller may cause the display to display an elapsed time in the tilted posture.

Abstract: A method includes disposing a plurality of actuators about a subject, each actuator being configured to generate a respective vibration signal, each vibration signal applying a normal force to the subject, and controlling the plurality of actuators such that the respective vibration signal of each actuator of the plurality has a respective vibration characteristic. Each actuator is oriented such that the respective vibration signal propagates along a longitudinal axis of the subject for stimulation of the subject remote from the plurality of actuators.

Abstract: A therapy device for treating left-side and right-side body parts comprises a single-piece base plate having a left surface and a right surface, a moving segment having a support surface for a left- or right-side body part to be treated, and a drive for pivoting the moving segment back and forth relative to the base plate. The moving segment is fastened to the base plate so as to be pivotable around an axis of rotation. The left surface of the base plate is shaped for supporting thereon a left-side body portion assigned to a left-side body part to be treated. The right surface of the base plate is shaped for supporting thereon a right-side body portion assigned to a right-side body part to be treated.

Abstract: A three-dimensional surface scan of an exoskeleton wearer is performed to generate three-dimensional surface data, and a three-dimensional surface model of the exoskeleton wearer is generated from the three-dimensional surface scan data. A three-dimensional exoskeleton model is generated from the three-dimensional surface model. At least one three-dimensional exoskeleton component is printed from the three-dimensional exoskeleton model, and a custom-fit exoskeleton is assembled using the at least one three-dimensional exoskeleton component.