Abstract: Rear tip extenders having a tether attached to a collar for penile implants that can be mounted onto a respective cylinder forward of a fluid line (that communicates with a scrotal pump) to prevent full separation or detachment from the cylinder during a revision procedure can be fabricated by molding. The fabrication methods include: providing a mold with a mold cavity configured to define three attached members of defined shapes, including a rear tip extender, a collar and a tether attaching the rear tip extender and collar; and flowably introducing moldable material into the mold cavity to form the collar, rear tip extender and attached tether as a molded assembly.

Abstract: A resorbable bone graft scaffold material, including a plurality of overlapping and interlocking fibers defining a scaffold structure, plurality of pores distributed throughout the scaffold, and a plurality of glass microspheres distributed throughout the pores. The fibers are characterized by fiber diameters ranging from about 5 nanometers to about 100 micrometers, and the fibers are a bioactive, resorbable material. The fibers generally contribute about 20 to about 40 weight percent of the scaffold material, with the microspheres contributing the balance.

Abstract: Devices and methods for in situ drawing, filtering and seeding cells from the marrow of surrounding bone into a fusion cage without any of the challenges mentioned above. Various implants and devices with aspiration ports that enable in-situ harvesting and mixing of stem cells. These devices may include spinal fusion cages, long bone spacers, lateral grafts and joint replacement devices. Each device utilizes at least one aspiration port for harvesting of stem cell-containing marrow via aspiration from adjacent bony elements.

Abstract: Instrumentation and assembly for arthroscopic elbow surgery which includes a humeral component. The humeral component is installed in a trough formed in the humeral condyle. The trough may be formed by using a plurality of drill pins and a plurality of corresponding cutters (and optionally a template). The two drill pins are passed through the template and drilled into the humerus, and cutters are advanced over the corresponding drill pins to form the trough. The humeral component may be employed in conjunction with an ulnar implant.

Abstract: A tibial base plate for attaching to a resected surface at a proximal end of a tibia is provided. The tibial base plate includes a bridge, a pair of compartments and a stem. The bridge has a first contact surface sitting on the resected surface. The compartments are disposed at opposite sides of the bridge and extend in an anterior-posterior direction to form a notch to accommodate a tibial eminence. Each of the compartments has a second contact surface sitting on the resected surface. The stem is connected to the bridge and the compartments and inset into the proximal end of the tibia. The stem has an outer surface. The outer surface is canted towards the notch as insetting into the proximal end of the tibia. The stem is engaged with a cutting slot on the resected surface into the proximal end of the tibia.

Abstract: A hand manipulated endoscopic medical device includes a body having a proximal end, which is hand manipulated, a distal end which includes a manipulator, a light emitting device at the distal end, an imaging device at the distal end. A tool for extracting an artificial lumbar disc from between a pair of vertebral plates includes a handle, a member for transmitting force, and a sharpened end, specially configured to be placed between the artificial disc and the vertebral plate. A tool for implanting or explanting a ball to or from an artificial lumbar disc includes a pinion shaft and a pinion shaft enclosure, with a tightening knob at the proximal end of the shaft enclosure and coupled to the pinion shaft, a pinion at the distal end of the pinion shaft, a grappling device at the pinion, and a pair of semi-circular rings.

Abstract: An orthopedic device for implanting between adjacent vertebrae comprising: an arcuate balloon and a hardenable material within said balloon. In some embodiments, the balloon has a footprint that substantially corresponds to a perimeter of a vertebral endplate. An inflatable device is inserted through a cannula into an intervertebral space and oriented so that, upon expansion, a natural angle between vertebrae will be at least partially restored. At least one component selected from the group consisting of a load-bearing component and an osteobiologic component is directed into the inflatable device through a fluid communication means.

Abstract: Embodiments herein are generally directed to vertebral implants and implant trials for use with vertebral implant assemblies. In some embodiments, these implants and implant trials may be used in conjunction with corpectomy procedures.

Abstract: Disclosed herein is an intervertebral disc prosthesis comprising a first cantilever arm; the first cantilever arm comprising a shaft that is affixed to a disc; a second cantilever arm that comprises a plurality of rods that contact the disc; the plurality of rods being equidistant from a central axis of the shaft; and a third cantilever arm that comprises a platform to which are attached a plurality of rings; the rings being concentrically disposed about the shaft; the rings being in operative communication with each other; where the plurality of rods contacts the platform; and where the second cantilever arm has more degrees of freedom than the first cantilever arm, while the third cantilever arm has a number of degrees of freedom that are greater than or equal to the number of degrees of the second cantilever arm.

Abstract: An intervertebral implant assembly includes and inserter tool and an implant having a U-shaped body shaped and dimensioned to be placed between two adjacent vertebras. The U-shaped body comprises a rounded front end, an open back end, first and second elongated components extending from the rounded front end, forming the U-shaped body and ending at the open back end and at least one rigid strut extending from and connecting opposite inner side surfaces of the first and second elongated components. A first through-opening is formed in the space between the front end, the rigid strut and the opposite inner side surfaces of the front portions of the first and second elongated components and a second through-opening is formed in the space between the open back end, the rigid strut and the opposite inner side surfaces of the back portions of the first and second elongated components. The inserter tool comprises a shaft, a middle sleeve and an outer sleeve that work together to attach and lock to the implant.

Abstract: A device for insertion into a spinal (intervertebral or intravertebral) space is expandable and contractable. The device includes a body assembly, a top member configured to fit within a gap in the body assembly, a drive gear disposed within the body assembly at a distal end of the body assembly, a proximal gear assembly, and a distal gear assembly. The drive gear includes a receiver accessible from outside the body assembly and configured to be rotated in order to rotate the drive gear. Each gear assembly is attached to the top member. The distal gear assembly engages the drive gear. Rotation of the drive gear in a first direction causes the gear assemblies to translate the top member away from the body assembly, and rotation of the drive gear in a second direction causes the gear assemblies to translate the top member towards the body assembly.

Abstract: An expandable spinal fusion implant including a housing, upper and lower endplates, a wedge positioned within the housing and between the upper and lower endplates and a drive mechanism to urge the wedge distally between the upper and lower endplates to increase the separation between the endplates and expand the overall height of the distal end of the implant.

Abstract: A modular surgical tool that is used to insert instruments into the intervertebral disc space of a patient to measure the height of the intervertebral disc space, to prepare the intervertebral disc space for an implant, and to insert the implant into the intervertebral disc space using a plurality of interchangeable tool ends. Advantageously, this modular surgical tool permits multiple insertion angles.

Abstract: A prosthetic liner and liner pin alignment device has a support, and a body extending from the support. The body has a cup defining an inner wall surface defining a liner-receiving recess having a longitudinal axis and defining a liner pin-receiving guide hole to a liner pin-receiving pin guide aperture. The liner pin-receiving pin guide aperture has a central axis parallel to the longitudinal axis of the liner-receiving recess.

Abstract: The subject invention is directed to devices and methods for producing devices for regulating blood flow in the venous system. In particular, the invention provides for artificial valves designed to regulate the flow of blood in human vessels, wherein such artificial valves include superior properties including fatigue resistance, biocompatibility, and ease of manufacture.

Abstract: Disclosed are liquid cast biodegradable arterial stents and methods for preparing liquid cast biodegradable arterial stents. The typically includes a biodegradable polymer and may include an agent for treating neointimal hyperplasia.

Abstract: A personalized prosthesis for implantation at a treatment site of a patient includes a self-expanding mesh or membrane having collapsed and expanded configurations. The collapsed configuration is adapted to be delivered to the treatment site, and the expanded configuration engages the personalized prosthesis with the treatment site. The mesh or membrane is personalized to match the treatment site in the expanded configuration, and has an outer surface that substantially matches the treatment site shape and size. The self-expanding mesh or membrane forms a central lumen configured to allow blood or other body fluids to flow therethrough. Methods of manufacturing and delivery of the personalized prosthesis are also disclosed.

Abstract: A personalized prosthesis for implantation at a treatment site of a patient includes a self-expanding mesh or membrane having collapsed and expanded configurations. The collapsed configuration is adapted to be delivered to the treatment site, and the expanded configuration engages the personalized prosthesis with the treatment site. The mesh or membrane is personalized to match the treatment site in the expanded configuration, and has an outer surface that substantially matches the treatment site shape and size. The self-expanding mesh or membrane forms a central lumen configured to allow blood or other body fluids to flow therethrough. Methods of manufacturing and delivery of the personalized prosthesis are also disclosed.

Abstract: A personalized prosthesis for implantation at a treatment site of a patient includes a self-expanding mesh or membrane having collapsed and expanded configurations. The collapsed configuration is adapted to be delivered to the treatment site, and the expanded configuration engages the personalized prosthesis with the treatment site. The mesh or membrane is personalized to match the treatment site in the expanded configuration, and has an outer surface that substantially matches the treatment site shape and size. The self-expanding mesh or membrane forms a central lumen configured to allow blood or other body fluids to flow therethrough. Methods of manufacturing and delivery of the personalized prosthesis are also disclosed.

Abstract: The invention relates to an implantable radiopaque stent adapted to be disposed in a body lumen. In one aspect of the invention, a plurality of elongate filaments including one or more radiopaque filaments are arranged to form a hollow tubular structure having a tubular wall that defines an inner surface and an outer surface and opposing first open end and second open end. One of the open ends of the stent is formed by an intersection of adjacent filament ends. A radiopaque compound is applied to the intersection, the radiopaque compound comprising radiopaque material and polymeric material. The radiopaque compound and radiopaque filament provide improved external imaging of the tubular structure on imaging equipment.

Abstract: A stent design reduces the likelihood of contact among structural members when the stent diameter is reduced before insertion into the body. In one approach, an undulating link has a J-shaped profile or has an angled portion on one side at the peak of the link, in order to reduce contact during crimping. The stent may also include structural features that improve such aspects as flexibility, the coatibility of a drug coating onto the stent, flare reduction, stent retention within the body and/or reduction of the minimum diameter of the stent during crimping.

Abstract: Described herein are flexible implantable occluding devices that can, for example, navigate the tortuous vessels of the neurovasculature. The occluding devices can also conform to the shape of the tortuous vessels of the vasculature. In some embodiments, the occluding devices can direct blood flow within a vessel away from an aneurysm or limit blood flow to the aneurysm. Some embodiments describe methods and apparatus for adjusting, along a length of the device, the porosity of the occluding device. In some embodiments, the occluding devices allows adequate blood flow to be provided to adjacent structures such that those structures, whether they are branch vessels or oxygen-demanding tissues, are not deprived of the necessary blood flow.

Abstract: A catheter system with a proximal end and a distal end element at the proximal end to actuate a device at the distal end of the system, and an actuator element (32) that runs the length of the system, from the actuator element to the device and actuates the device by transmitting a physical force from the proximal end to the distal end and characterized by a pre-tensioner (40) near the distal end of the system, that can be set in a pre-tensioning disposition prior to actuation of the device, the pre-tensioner thereby reducing the magnitude of the physical force that must be transmitted from the proximal end when actuation of the device is required.

Abstract: A stent indwelling device includes a guide catheter and a pusher catheter. The guide catheter includes: a core section; an outer layer section surrounding an outer circumference of the core section; a stent protection section disposed between the core section and the outer layer section, being longer than a dimension of a tube stent, having stiffness resisting compression inward in a radial direction perpendicular to a longitudinal axis of the guide catheter, and having flexibility in a direction in which the guide catheter is curved; and a stopper configured to allow expansion of the stent protection section in a direction along the longitudinal axis and restrict movement of the stent protection section in the direction with respect to the core section.

Abstract: A variety of passive intragastric implant devices for obesity treatment are disclosed. Such passive devices do not autonomously change shape, but instead react within the stomach to induce satiety. The devices may take up volume within the stomach, thus reducing the intake capacity. Additionally, the devices may contact areas within the stomach, such as the cardia surrounding the esophageal sphincter, or the greater and lesser curvatures in the middle of the stomach, to stimulate satiety-inducing nerves. Some devices may combine two or more of these satiety-inducing features. Methods of implant are disclosed including compressing the devices within a delivery tube and transorally advancing the devices through the esophagus to be deployed within the stomach. Removal of the devices occurs in the reverse.

Abstract: A gastrectomy device includes an elongated member and a tube. The elongated member has a proximal end and a distal end and defines a longitudinal side window disposed adjacent the distal end. The elongated member defines a first longitudinal channel, a second longitudinal channel, and a plurality of side apertures. The first longitudinal channel is in communication with the longitudinal side window and the plurality of side apertures is in communication with the second longitudinal channel. The tube extends through the first longitudinal channel. An array of lights is associated with the tube to provide illumination. The tube is movable through the elongated member between a first state, in which the tube is disposed within the first longitudinal channel of the elongated member, and a second state, in which a portion of the tube extends through the longitudinal side window of the elongated member.

Abstract: A prosthesis that when implanted in the gastrointestinal tract does not impede the normal function of the pyloric sphincter. In some instances, the prosthesis is implanted as part of, or after, a sleeve gastrectomy procedure. The prosthesis includes a stent with an outer surface and a polymeric cover fully covering the outer surface of the stent. The stent includes a proximal stent flange; a proximal stent segment extending distally from the proximal stent flange; and an enlarged stent segment extending distally from the proximal stent segment.

Abstract: A limb protective covering (10) includes an elongated sleeve (11) and an adjustable, elastic retaining strap (12). The sleeve has a closed end (15) and an open end (16) opposite the closed end. The sleeve is made of a high performance elastomeric polymer blend, such as a styrene-butadiene-styrene (SBS) based monolayer elastomeric antistatic film having a coefficient of friction of at least 0.6.

Abstract: A back plate of a waist support includes a supporting section and two wings. The supporting section has a valley portion for receiving a wearer's spine. The two wings are symmetrically connected to the supporting section from two widthwise opposite sides thereof and each have plural lengthwise grooves, for making the wings of the back plate bendable. Thereby, the waist support is endurable and supportive and can effectively distribute the load that is focused on of the wearer's lumbar vertebrae.

Abstract: Systems and methods for treating a patient's mucus hypersecretion condition are disclosed herein. Certain implementations may involve a method for reducing mucus secretion in an upper airway of a patient to treat at least one of post nasal drip or chronic cough. The method may include advancing a treatment delivery portion of an energy-based treatment device into a nostril of the patient. The treatment delivery portion may contact mucosal tissue of the upper airway without piercing the mucosal tissue. The treatment delivery portion may deliver treatment to at least one tissue selected from the group of the mucosal tissue and another tissue underlying the mucosal tissue to modify a property of the at least one tissue and thus treat at least one of post nasal drip or chronic cough in the patient.

Abstract: A connecting device is made available for connecting the distal part of a penis to a penis extension device, wherein the connecting device (1) has an elongate, rigid hollow body (3), which is open at the proximal end and is used for receiving the distal end of the penis and for securing on the penis extension device and, at its distal end, has an opening (31) that is in operational connection to a vacuum pump (4) or can be brought into such an operational connection, and an elastic tubular sleeve (2) which is placed with its proximal area (5) onto the shaft of the penis and which, when the connecting device (1) is in the assembled state, has its distal area (6) enclosing the proximal end of the hollow body (3) and bearing on the outside thereof.

Abstract: An ostomy appliance is sufficiently small to provide the user with a desired level of discretion, and can also provide an expanded collection capacity to accommodate sudden outflows of stomal discharge.

Abstract: A tongue grasping and restraining device holds the tongue securely during sleep in order to minimize the risk of the tongue slipping back and blocking the throat. Plural tongue gripping projections are coupled to upper and lower supports. One or more of the upper and lower supports are biased together into a tongue engaging position. A tongue depressor can extend rearwardly and downwardly from the upper support to depress the user's tongue to further open the user's airway. The position of the tongue depressor can be adjustable. The upper support is coupled to the user's upper jaw, for example, to a denture, dental appliance or other form of an upper jaw coupler and can be pivoted thereto. The lower support can be hinged to, fixed to, or otherwise joined to a lower jaw coupler. A tube and rod mechanism can couple the jaw couplers together.

Abstract: A system includes a heat exchange catheter line assembly configured to convey working fluid circulating to and from at least one heat exchange element on an intravascular heat exchange catheter. The system also includes a heat exchange system that itself includes a processor and is configured for fluidly communicating with the heat exchange catheter line assembly to exchange heat with the working fluid. A near field communication (NFC) member associated with the heat exchange system and an NFC element associated with the heat exchange catheter line assembly are also included. The NFC member is configured to provide the processor with a signal representative of whether the NFC member detects the NFC element.

Abstract: This invention provides for a device and methods of dispensing a precise predetermined volume of liquid of discrete drops, vapor, or mist while preventing contamination due to Pull Back and ensuring precision dispensing.

Abstract: An apparatus for controlled healing of ocular erosions is described. The apparatus comprising; an optical surface comprising an energizable controller capable of being programmed to transmit energy from an energy source onto/into an ocular surface, through the use of a current generator in electrical connection with energy emitting contacts capable of transmitting an electric field. The controller, current generator and energy emitting contacts are biocompatible or encapsulated by a conductive biocompatible layer to allow positioning of said apparatus in an ocular surface.

Abstract: Provided is a configuration in which when a positioning member is removed from an intraocular lens insertion tool, restrictions on the position and posture of an intraocular lens can be lifted smoothly without exerting influence on the intraocular lens and the insertion tool itself. The present invention is provided with: an approximately cylindrical nozzle body (10); a stage part which is provided in the nozzle body (10) and houses an intraocular lens; a plunger which presses the intraocular lens housed in the stage part by the forward end thereof to discharge the intraocular lens into an eyeball; and a positioning member (60) which restricts the initial position and posture of the intraocular lens by being mounted to the stage part from the outside.

Abstract: A test device to calibrate the pulse energy of a laser device which provides pulsed laser radiation includes a measuring head with multiple measuring probes. The test device is used in such a way that by means of the laser radiation, multiple test ablations are made on a test surface, in an arrangement corresponding to the relative spatial arrangement of the measuring probes, and the depths of the test ablations are then measured, with simultaneous use of the multiple measuring probes of the measuring head.

Abstract: A process of manufacturing a wound dressing filler and/or wound dressing.

Abstract: A method for producing a multi-layered absorbent article is disclosed. At least two of the layers include a colored region.

Abstract: A converting apparatus operates to transfer a folded absorbent article from a first carrier apparatus to a second carrier apparatus. The converting apparatus includes a transfer apparatus and a guide member located adjacent to the transfer apparatus, forming a gap there between. The transfer apparatus includes a frame that is rotatable about a first axis of rotation and a transfer member that is rotatable about a second axis of rotation. The transfer member defines a receiving surface and the guide member defines a guide surface. The guide surface converges toward the receiving surface. The frame advances the absorbent article in a machine direction through the gap. While advancing absorbent article advances through the gap, the transfer member rotates the absorbent article about the second axis of rotation. The guide member includes side seam tuckers that are adapted to tuck the side seams of the absorbent article.

Abstract: A disposable wearing article includes a urination region to be in contact with a urination unit of the wearer, a buttocks region to be in contact with buttocks of the wearer, and an absorbent sheet which includes an absorbent polymer sandwiched between liquid-impermeable layers. The absorbent sheet is disposed in the buttocks region but not in the urination region.

Abstract: The present invention relates to an odor control material consisting of a water-insoluble particulate odor control agent and a thermoplastic water-soluble carrier matrix encapsulating the odor control agent. The carrier matrix dissolves when in contact with an aqueous solution, such as urine and the odor control material is obtained by means of thermoforming. The invention relates also to a method for the preparation of the odor control material and the use of the odor control material in absorbent products. The present odor control material minimizes dusting problems caused by particulate odor control agents in production processes.

Abstract: A wheelchair frame comprises a base frame having a geometry that is structured and configured to be adjustable about a fixed pivot, wherein the base frame comprises a central frame and frame component that are adjustable via an angular adjustment.

Abstract: A patient support is provided. The patient support may include a plurality of inflatable members that raise or lower portions of the patient support based on the status of a valve assembly. The patient support may also include a plurality of inflatable members positioned at a foot end of the patient support to support lower legs of a patient including their heels. Another valve assembly is provided to control a bleed rate of air from the heal bladders.

Abstract: Disclosed is a manual lifting sling apparatus (10) made of fabric, comprising: a bottom support part (12) used for supporting the buttocks and legs of a patient; a rear support part (11) joined to the bottom support part (12) to form an inclined angle and used for supporting the back of the patient; a left blocking part (13) and a right blocking part (14) restraining the patient respectively on the left and right sides, the left blocking part (13) and the right blocking part (14) both concurrently being joined with the bottom support part (12) and the rear support part (11); and at least two lifting handles (15) provided on both the left blocking part (13) and the right blocking part (14). The fabric used for the apparatus is a woven fabric or non-woven fabric, and is made of a non-biodegradable material or biodegradable polymer material.

Abstract: The present application includes a system for separating solid and liquid waste through a bedpan. The system includes the bedpan, a screen member, and a storage member for liquid waste. Liquid waste is passed through the screen within the bedpan and into the storage member. The storage member is externally located outside of the bedpan. The storage member is configured to visual access by a medical professional to permit an ease of measurement and detection of liquid waste collected. The storage member is detachable and can be closed to prevent spillage during transportation.

Abstract: A method and system tilts an infant-care medical device. In one example, the method and system pivots the infant-care device about the tilt axis by releasing a tilt platform of the infant-care medical device using an actuator to allow the tilt platform to pivot about the tilt axis. The method and system also selectively adjusts a rotational position of the tilt platform relative to a tilt axis. As the tilt platform pivots about the tilt axis, the system and method dampens pivoting of tilt platform using a damper. As so dampened, the pivoting of the tilt platform is counter-balanced such that vibration and/or movements that may be felt by an infant within the infant-care medical device may be reduced.

Abstract: A limb holder comprising: a mounting bracket for attachment to a surgical table; a mounting element comprising a spheroidal surface for attachment to said mounting bracket; a clamping assembly for providing a clamping engagement about said spheroidal surface of said mounting element, said clamping assembly comprising an upper jaw and a lower jaw, wherein said upper jaw and said lower jaw are biased towards one another so as to provide said clamping engagement about said sphereoidal surface of said mounting element; a limb support element mounted to said clamping assembly via a support rod; and a release mechanism mounted to said support rod and connected to said clamping assembly for selectively releasing said clamping engagement of said clamping assembly about said sphereoidal surface of said mounting element, whereby to allow said limb support element to be repositioned relative to said mounting element and hence repositioned relative to the surgical table.

Abstract: A system and method by which movements desired by a user of a lower extremity orthotic is determined and a control system automatically regulates the sequential operation of powered lower extremity orthotic components to enable the user, having mobility disorders, to walk, as well as perform other common mobility tasks which involve leg movements, perhaps with the use of a gait aid.