Abstract: A deflectable device, such as a catheter, is provided that includes a hinge that enhances the ability of the device to deflect or bend within a predetermined plane. The catheter comprises an elongated tubular catheter body having proximal and distal ends and at least one lumen extending therethrough. A distal segment is provided distal to the distal end of the catheter body. A tubular hinge is provided between the distal end of the catheter body and the proximal end of the distal segment. The hinge has an axis and at least one lumen extending therethrough. The tube includes at least one slot, and preferably a plurality of slots, extending part of the way through the hinge generally transverse to the axis of the hinge.

Abstract: The invention generally relates to method and apparatus for crossing an obstruction in a tubular member, and more particularly to a medical device method for crossing of a chronic occlusion in a subintimal or interstitial space of an artery.

Abstract: Described are peritoneal catheter devices and methods for positioning these devices in a medical patient. The peritoneal catheter includes a catheter tube having a proximal end portion opposite a distal end portion, a stationary flange attached to the catheter tube near the distal end portion, and a mobile flange positioned on the catheter tube between the stationary flange and the proximal end portion. In use, the stationary flange is positioned to cover a hole in the rectus muscle and the mobile flange is selectively moved along the catheter tube to sandwich the rectus muscle of the patient between the stationary flange and the mobile flange. Optionally an interior cuff is mounted on the catheter tube adjacent to the stationary flange but between the stationary flange and the mobile flange and wherein the selectively positioning the mobile flange includes sandwiching the interior cuff between the stationary flange and the mobile flange.

Abstract: An apparatus comprises an absorbent body, a non-permeable feature, and a port feature. The absorbent body comprises a wicking feature. The non-permeable feature is coupled with the absorbent body. The non-permeable feature and at least a portion of the absorbent body are configured to fit in an opening in a paranasal sinus wall. The port feature extends through the absorbent body. The port feature defines a lumen. The wicking feature extends outwardly relative to the port lumen. During installation of the apparatus, the non-permeable feature is positioned in an opening in the paranasal sinus wall. The absorbent body is oriented such that the wicking feature is in contact with mucosal tissue in a sinus cavity defined by the paranasal sinus wall. A proximal portion of the absorbent body is positioned outside the paranasal sinus wall.

Abstract: Various embodiments disclosed herein relate to an implantable device, systems, and methods related thereto, that includes at least one sensor and/or therapeutic agent delivery depot. In one embodiment, the system and device include means for detecting general or specific biological agents in a subject's intestinal tract, and utilizing the information from the detection for determining the timing and content of any therapeutic treatment needed by the subject.

Abstract: Devices for the local delivery of microdose amounts of one or more active agents, alone or in combination, in one or more dosages, to selected tissue of a patient are described. The devices generally include multiple microwells arranged on or within a support structure and contain one or more active agents, alone or in combination, in one or more dosages and/or release pharmacokinetics. In an exemplary embodiment, the device has a cylindrical shape, having symmetrical wells on the outside of the device, each well containing one or more drugs, at one or more concentrations, sized to permit placement using a catheter, cannula, or stylet. Optionally, the device has a guidewire, and fiber optics, sensors and/or interactive features such as remote accessibility to provide for in situ retrieval of information and modification of device release properties. In a preferred embodiment, the fiber optics and/or sensors are individually accessible to discrete wells.

Abstract: A transdermal drug delivery device is disclosed that may comprise a housing including an upper housing portion and a lower housing portion. The lower housing portion may define a bottom surface including skin attachment means for releasably attaching the lower housing portion to skin of a user. The upper housing portion may at least partially surround a central region of the device. The device may also include a microneedle assembly and a reservoir disposed within the central region. The reservoir may be in fluid communication with the microneedle assembly. Additionally, the device may include a pushing element disposed above the microneedle assembly within the central region. The pushing element may be configured to provide a continuous bilateral force having a downward component transmitted through the microneedle assembly and an upward component transmitted through the skin attachment means.

Abstract: A method of power injecting a contrast medium into a patient, including obtaining a power-injectable access port suitable for power injection. The power injectable access port includes a housing defining a reservoir, and a septum. The septum may include a self-sealing material, and a radiopaque material. The radiopaque material may form a selected pattern when an x-ray is taken through the septum for identifying the power-injectable access port as being suitable for power injection. The power-injectable access port may be structured for accommodating a pressure developed within the reservoir of at least 35 psi, and may be designed to accommodate a fluid flow rate of at least 1 milliliter per second. After implanting the power-injectable access port in the patient, the method may include imaging the power-injectable access port and confirming via the selected pattern in the septum that the power-injectable access port is suitable for injecting the contrast medium.

Abstract: A connecting structure for medical use includes a first connecting portion 1 and a second connecting portion 2. The first connecting portion 1 includes a threadedly engageable portion 22a, a support portion 22b and a sealing portion 14. The second connecting portion 2 includes a threadedly engageable portion 2c and a sealing portion 2b. The threadedly engageable portions are threadedly engageable with each other. The sealing portions are joinable to each other by advancement of a threaded engagement between the threadedly engageable portions. An operating cylinder 30 is mounted on an outer periphery of the support portion 22b. A torque limiting mechanism 40 is disposed between the operating cylinder 30 and the support portion 22b. The sealing portions 14, 2b can be joined by turning the operating cylinder 30 in a threaded engagement advancing direction.

Abstract: Constriction valves for catheters and method of using constriction valves are presented. The catheter valve has a conduit defining a lumen. The catheter also has a spring that is configured to bias the lumen from an open position to a closed position by altering an effective length of the conduit or altering the circumference of the conduit. The spring is further configured to change its configuration by changes of intraluminal pressure of the valve. A user can insert a tool into a catheter having a valve by manipulating the valve to expand a substantially closed lumen by compressing the spring, twisting the spring, or pulling on a cord coupled with the valve.

Abstract: A wearable therapeutic device includes a garment configured to be worn on a torso of a patient. The garment has an anterior portion and a posterior portion. The garment is configured to house at least one defibrillator component, a first therapy electrode disposed in the anterior portion of the garment, a second therapy electrode disposed in the posterior portion of the garment, and an alarm module configured to alert the patient of an impending defibrillation shock from the at least one defibrillator component to be delivered by at least one of the first therapy electrode and the second therapy electrode. The first therapy electrode and the second therapy electrode are configured to be electrically coupled to the at least one defibrillator component. At least one of the first therapy electrode and the second therapy electrode is at least one of woven into the garment and comprises a textile material.

Abstract: A microlead, of an overall diameter less than 0.5 mm, includes a plurality of at least eight conductor wires individually insulated and twisted together. Each conductor wire includes an electrically conductive core microcable and an insulation layer surrounding the core microcable and having at least one exposed area to form a detection/stimulation electrode of the microlead. The microlead further includes a central support structure shaped as a surface of revolution, which may be free of conductor wires and of central lumen. The conductor wires are configured in one or more layers of twisted peripheral conductor wires carried by the central support structure and circumferentially distributed thereon.

Abstract: A coiled, closed-loop RF current attenuator is configured to be placed about an implantable lead conductor. A coiled conductor extends in a coiled shape defining a longitudinal axis from a first coil end to a second coil end. The first coil end is electrically connected to the second coil end. An insulator is disposed about the coiled conductor. The closed loop attenuator can also include in series a short, a capacitor and/or a resistor. In some embodiments the closed loop attenuator can be resonant at an MRI RF-pulsed frequency. The closed loop attenuator can be integrated as a permanent part of an implantable lead conductor, or alternatively, be a stand-alone device that is placed about a premade implantable lead conductor.

Abstract: Systems and methods for controlling a tissue of a subject using applied pulsed electric fields. The system for controlling a therapy provided to a tissue of a subject using applied pulsed electric fields. The system includes an electrode assembly configured to engage a skin tissue of a subject to deliver a series of electric field pulses to the skin tissue and a user input configured to receive an operational instruction for the series of electric field pulses. The operational instruction defines at least one of a pulse duration, a pulse frequency, a pulse number, and a pulse amplitude. The system also includes at least one processor configured to access the operational instruction received by the user input and, using the operational instruction, create an electric field profile to be generated by the electrode assembly about the skin tissue of the subject to control a fibroblast characteristic while preserving a vascular perfusion in at least a portion of the skin tissue.

Abstract: Presented herein are techniques for optimizing stimulation parameters for use in a stimulating auditory prosthesis based on a recipient's cognitive auditory ability.

Abstract: A method of reducing renal hypertension applied for electrically stimulating a target zone of an organism having a symptom of renal hypertension by using an electronic stimulation device. The electronic stimulation device comprises at least one electronic stimulation unit. The electronic stimulation unit includes at least one first electrode and at least one second electrode. The method includes the following steps. The electrical stimulation unit is placed near the target zone. The electrical stimulation unit generates an electrical stimulation signal and the electrical stimulation signal is introduced to the target zone so as to stimulate the target zone. An electric field is generated between the first electrode and the second electrode and covers the target zone. The strength of the electric field ranges from 100 V/m to 1000 V/m.

Abstract: Methods, medical devices, and magnetic resonance imaging (MRI) systems are provided. A patient implanted with a medical device is exposed to a time-varying magnetic field having a signature, thereby inducing mechanical vibrations in at least one component of the medical device. A vibrational characteristic of the mechanical vibrations induced in the component(s) is detected. The vibrational characteristic is analyzed, and the signature of the magnetic field is identified based on the analyzed vibrational characteristic. The medical device is automatically switched from a first operational mode to a second operational mode when the signature is identified.

Abstract: An example of a system for programming a neurostimulator may include a storage device and a pattern generator. The storage device may store a pattern library and one or more neuronal network models. The pattern library may include fields and waveforms of neuromodulation. The one or more neuronal network models may each be configured to allow for evaluating effects of one or more fields in combination with one or more waveforms in treating one or more indications for neuromodulation. The pattern generator may be configured to construct and approximately optimize a spatio-temporal pattern of neurostimulation and/or its building blocks using at least one neuronal network model. The spatio-temporal pattern of neurostimulation may include a series of sub-patterns for treating an indication of the one or more indications for neuromodulation.

Abstract: Electrical stimulation of a target (e.g., nervous tissue) is performed, wherein balance phases are automatically determined, and at least one of the electrodes is indirectly monitored during therapy delivery. The stimulation system is further configured to generate correction currents when a voltage accumulated at associated double layer capacitances crosses pre-defined thresholds so as to reduce or cancel the accumulated voltages without therapy interruption. A finer automatic determination of balance phases permits minimizing the stimulus artifact for evoked response sensing. Closed-loop neurostimulation may be performed based on such evoked responses.

Abstract: Systems and methods may facilitate selection of a vector for delivering electrical stimulation to a patient's heart. One illustrative method may include delivering electrical stimulation at a first voltage to each vector in a first set of two or more vectors of a multi-vector medical system, determining whether the delivered electrical stimulation at the first voltage resulted in capture for each of the vectors in the first set of two or more vectors, identifying those vectors of the first set of two or more vectors that were determined to result in capture as a second set of vectors, delivering electrical stimulation at a second voltage that is lower than the first voltage to each vector in the second set of vectors, and determining whether the delivered electrical stimulation at the second voltage resulted in capture for each of the vectors in the second set of vectors.

Abstract: An implantable medical device for implantation into a patient may include a housing, a pulse generation circuit disposed at least partially within the housing, a plurality of electrodes electrically coupled to the pulse generation circuit, the plurality of electrodes being exposed external to the housing, and a controller operatively coupled to the pulse generation circuit. The controller may be configured to command the pulse generation circuit to deliver a phasic conducted communication pulse via at least two of the plurality of electrodes. Additionally, the phasic conducted communication pulse may comprise a first phase having a first polarity followed by a second phase having an opposite second polarity, wherein the second phase may have a duration of less than 60 microseconds, and wherein the first phase having may have a duration of between five percent and eighty percent of the duration of the second phase.

Abstract: The present invention is directed toward a detection architecture for use in implantable cardiac rhythm devices. The detection architecture of the present invention provides methods and devices for discriminating between arrhythmias. Moreover, by exploiting the enhanced specificity in the origin of the identified arrhythmia, the detection architecture can better discriminate between rhythms appropriate for device therapy and those that are not.

Abstract: A method, system, and apparatus for monitoring a magnetic field related to magnetic stimulation may be provided. A system for monitoring a pulsing magnetic field related to magnetic stimulation therapy may include a magnetic stimulation component, a sensor, and a processor. The magnetic stimulation component may be configured to generate the pulsing magnetic field for the magnetic stimulation therapy. The sensor may be configured to generate a signal associated with the pulsing magnetic field. The processor may be configured to estimate a first characteristic associated with a first peak of the signal, estimate a second characteristic associated with a second peak of the signal, and determine a third characteristic of the signal based on the first characteristic and the second characteristic. The processor may be configured to determine whether a failure occurred based on the third characteristic of the signal.

Abstract: There is provided a content output device including a selection unit which selects content according to a user's condition and a magnetic field pattern corresponding to the content, a content output unit which outputs the content, and a magnetic field generating unit which generates a magnetic field based on the magnetic field pattern.

Abstract: One bracelet embodiment provides therapeutic blood irradiation at a first wrist region using a first module, and body temperature regulation/irradiation at a second wrist region using a second module. A connector couples one end of the modules together, while an attachment band releasably couples the second ends together, for attachment to the wrist. The first module includes first and second distributed pluralities of lights respectively emitting 850 and 660 nm wavelengths, and a third plurality emitting 630 nm, 532 nm, and 450 nm wavelengths, positioned in a row substantially parallel to the arm of the user. The second module includes first and second rows of lights on first and second sides of a cooling unit, each emitting 405 nm wavelengths, with the two rows positioned for penetration to the radial and ulnar arteries. The bracelet includes a microprocessor, LED screen, and firmware for displaying a GUI permitting treatment protocol selections.

Abstract: A catheter treatment apparatus comprises an elongate tubular member and an expandable support. The expandable support comprises a radioactive substance to treat cancerous tissue and is configured to expand from a narrow profile for insertion to a wide profile to engage and treat tissue remaining after resection. The expandable support can be sized to fit within a volume of removed tissue to place the radioactive substance in proximity to the capsule and remaining tissue, to spare the capsule and proximate nerves and vessels to treat tissue in proximity to the capsule. The elongate tubular member may comprise a channel such as a lumen to pass a bodily fluid such as urine when the expandable support engages the tissue to treat the patient for a plurality of days. The treatment apparatus can be used to resect and diagnose tissue concurrently. Based on the diagnosis, targeted segmental treatment may be given.

Abstract: A therapeutic apparatus comprising: a magnetic resonance imaging system adapted for acquiring a set of magnetic resonance imaging data in an imaging zone, the magnetic resonance imaging system comprising a means for generating a magnetic field, —a guiding means adapted for guiding a beam of charged particles to a target zone within a subject, wherein the imaging zone comprises the target zone, a zone determination means adapted for determining the location of the target zone within the subject using the set of magnetic resonance imaging data, a trajectory calculation means adapted for calculating a trajectory of the beam using magnetic field data being descriptive of the magnetic field such that the calculated trajectory reaches the target zone, a control means adapted for controlling the guiding means using the calculated trajectory such that the beam follows the calculated trajectory.

Abstract: Images obtained by a camera system (10) arranged to obtain stereoscopic images of a patient (20) undergoing radio-therapy are processed by a modeling unit (56,58) which generates a model of the surface of a patient (20) being monitored. Additionally the patient monitoring system processes image data not utilized to generate a model of the surface of a patient being monitored to determine further information concerning the treatment of the patient (20). Such additional data can comprise data identifying the relative location of the patient and a treatment apparatus (16). This can be facilitated by providing a number or retro-reflective markers (30-40) on a treatment apparatus (16) and a mechanical couch (18) used to position the patient (20) relative to the treatment apparatus (16) and monitoring the presence and location of the markers in the portions of the images obtained by the stereoscopic camera (10).

Abstract: A control system for providing a closed loop, real time control of a charged particle pencil beam is disclosed. The system includes a first detector apparatus, a second detector apparatus, a first orthogonal magnetic deflector apparatus, a second orthogonal magnetic deflector apparatus, and a controller. The controller compares the measured position and beam angle of the beam with a model position and beam angle of a model beam to determine an offset error and a beam angle error. The first orthogonal magnetic deflector apparatus includes a pair of electromagnets to correct a first component of the offset and beam angle errors. The second orthogonal magnetic deflector apparatus includes a pair of electromagnets to correct a second component of the offset and beam angle errors. The beam can be iteratively adjusted during patient therapy or short pauses in patient therapy.

Abstract: In various embodiments, a radiation therapy method can include loading a planning image of a target in a human. In addition, the position of the target can be monitored. A computation can be made of an occurrence of substantial alignment between the position of the target and the target of the planning image. Furthermore, after the computing, a beam of radiation is triggered to deliver a dosage to the target in a short period of time (e.g., less than a second).

Abstract: A system (100) for and a method of visualizing quality information to a person performing a procedure of temporarily or permanently placing energy provision sources in a part of a body of a living being are provided. The body comprises a volume of interest. The system (100) comprising an input (104) for receiving a treatment plan (102), a data storage (108) for storing positions (P1, P2) of previously placed energy provision sources, a sub-system (106) for determining a shape and a position of the volume of interest, a tracking system (107) for obtaining tracking information relating to a placement tool for guiding a to-be-placed energy provision source towards a specific position, a processing device (110) configured for calculating a dose-volume histogram (114) for the volume of interest, and a display device (112) for presenting the dose-volume histogram (114) to the person.

Abstract: An ion chamber has a chamber having an interior volume. There is a first electrode and a second electrode in the chamber and separated by a gap. A collector electrode is positioned between the first electrode and the second electrode. The collector electrode is shaped to occlude a portion of the first electrode from the second electrode.

Abstract: Various embodiments, described herein, provide methods and systems for the treatment of plantar fascia. In some embodiments, a method of non-invasive treatment of plantar fasciacan include the steps of identifying a damage location comprising a planter fascia; directing a conformal distribution of ultrasound energy to the plantar fascia at the damage location; creating a plurality of micro lesions in the plantar fascia at the damage location; initiating healing of a plurality of micro tears in the plantar fascia at the damage location; and sparing intervening tissue between the plantar fascia and a surface of a sole of a foot.

Abstract: An apparatus and method for modifying collagen containing dermal tissue. The apparatus includes a source of ultrasound energy comprised of a plurality of curvilinear ultrasound transducers shaped to direct ultrasound energy to selected skin depths. The transducers have variable curvature, drive frequency, power level and geometries to effect precise control of collagen modification.

Abstract: A closed circuit breathing apparatus (2) and a method of operating the same, the method comprising: determining whether a sufficient amount of replenishing gas is being supplied to a breathing circuit (4); sensing pressure within the breathing circuit (4) using a pressure sensor (6); generating a pressure signal representative of the sensed pressure; determining whether the pressure signal is representative of breathing; and generating an alert if it is determined that both an insufficient amount of replenishing gas, such as oxygen, is being supplied to the breathing circuit (4) and that the pressure signal is representative of breathing.

Abstract: A fall arrest apparatus including a force damping subsystem having a damper, a brake release mechanism connected to the force damping subsystem and arranged to trigger when a force having a sufficient magnitude is transmitted to the brake release mechanism, and a brake mechanism including an energy storage device arranged to deploy at least one anchor when the brake release mechanism is triggered. The force is provided by a falling object to the force damping subsystem and the force damping subsystem is arranged to decelerate the falling object after the brake release mechanism is triggered.

Abstract: Fire suppression systems and methods of suppressing fires are disclosed. A fire suppression system may include a housing including inlet and outlet ports, and a housing interior having a fluid passage sized to contain a fire suppressing fluid source between the inlet and outlet ports. The inlet and outlet ports may be fluidly connected to the fluid passage. The system may additionally include a fluid discharge assembly configured to discharge fire suppressing fluid from a flow control assembly into the fluid passage and toward the outlet port. At least one of the fluid passage and the fluid discharge assembly may be configured such that the discharge of the fire suppressing fluid into the fluid passage draws air into the fluid passage through the inlet port and around the fire suppressing fluid source, and expels air and the fire suppressing fluid out of the fluid passage and through the outlet port.

Abstract: A method of utilizing a catalyst for the sterilization, disinfection and purification of indoor air. The catalyst carrier is made of inorganic porous material such as Silica, Zeolite, Diatomite, Sepiolite, Montmoroillonite, and Aluminum oxide. The catalyst carrier can also be made of Cordierite, or Mullite ceramic honeycomb. After dipping into stabilized sodium hypochlorite solution or stabilized chlorine dioxide solution, the catalyst is produced after dehydration. The catalyst is irradiated with ultraviolet lamp to generate gas-phase free radicals including reactive particles such as .OH, .ClO2, .HO2, .O, thereby sterilizing microbial air pollutants such as viruses, bacteria, fungi and other microorganisms, and remove chemical air pollutants such as formaldehyde.

Abstract: The present invention is an exercise ring accessory device that quickly inserts onto a set of exercise rings for ring strength training as used in gymnastics, cross-fit, and other strength programs that utilize exercise rings. The quickness and ease of installation and removal is a great value for coaches and users, as they can work more drills in less time. The device also provides a comfortable grip, and includes a cutout on the underside, allowing an elastic support band to be placed underneath device to give support to users of varying skill levels.

Abstract: A physical therapy system includes a rehabilitation device with a limb supporting plate configured to support a limb of a patient, a fastener securing the limb to a first surface of the plate, and a plurality of sliding or rolling elements attached to a second surface of the plate. The rolling/sliding elements may facilitate movement of the plate without directional bias. A deployment surface includes a substantially flat surface configured so the limb rehabilitation device may roll or slide over the flat surface, first and second raised edges attached the flat surface, and a measuring scale to facilitate measurement of the range of motion of the limb rehabilitation device over the deployment surface. The first raised edge and the second raised edge are configured to confine motion of the limb rehabilitation device over the deployment surface.

Abstract: A portable and removable mounted exercise station includes an elongated anchoring member disposed on a surface of an external stationary object, such as a wall. The anchoring module has a doorknob shaped cleat, a plurality of knobs, and brackets formed in both ends of the elongated anchoring member. A corner mounting adapter to mount the station in a corner where two walls meet. A resistance band connects to one of the knobs to provide resistance during an exercise routine. A clip allows for quick connect and disconnect of the resistance band to the station.

Abstract: A motor-less leg-powered curved treadmill produced that allows people to walk, jog, run, and sprint without making any adjustments to the treadmill other than shifting the user's center of gravity forward and backwards. A closed loop treadmill belt running between front and rear pulley rollers is formed with a low friction running surface of transverse aluminum, wooden, plastic, rubber or carbon fiber slats attached to each other in a resilient fashion. Since an essential feature of treadmill is the concave shape of the running surface of belt in its respective upper portion, the treadmill configurations insure that this shape is maintained during actual use. These configurations prevent the concave upper running surface portion from being pulled taut into a flat shape between the front and rear pulley rollers.

Abstract: A therapeutic hand-held exercise device includes a pair of movable members that each define a handle portion and an end effector portion. The movable members are pivotably connected for relative pivotal movement between a first position and a second position. The handle portion of one of the movable members defines at least one flexible member engaging post. The end effector portion of the other movable member defines at least one flexible member engaging post such that the flexible member engaging posts can receive a common flexible member. The flexible member engaging posts are joined via a first common flexible member and other flexible member engaging posts are joined via a second common flexible member. The common flexible members may each exhibit a tensile strength that provides resistance to movement which either differs from or is equal to the tensile strength of the other common flexible member.

Abstract: A fitness monitor comprises a housing, a wrist band, a motion sensor, a display, a non-transitory memory element and a processing element. The wrist band is coupled to the housing and configured to attach to a wrist of a user. The motion sensor is configured to sense motion of the user and generate motion data. The display is coupled to the housing and configured to present information associated with user activity. The memory element is located in the housing and configured to store the activity data and a daily activity goal. The processing element is operably coupled to the memory element and configured to determine daily activity data, a daily activity goal corresponding to a predetermined level of activity for the user, compute an activity countdown and level of inactivity, and present, on the display, the activity countdown and inactivity indicia indicating the level of inactivity.

Abstract: A rebound and balance training device includes a frame, a footboard, a carrier for the footboard and a plurality of resilient spring elements extending between and attached to the frame and the carrier to support the footboard above a supporting surface. A user standing on the footboard manually effects repeated vertical bouncing movement between upper and lower positions. The distance traveled by the footboard, the effort required to effect movement, and the stability thereof may be modified by selectively modifying the number, the length, the position, or the elasticity of the resilient elements. In one embodiment, a pair of footboards is employed to simulate skiing movements.

Abstract: A golf ball dimple pattern based on a hexagonal dipyramid is disclosed. The dimples are arranged based on six substantially similar dimple sections on each of the two hemispheres of the ball.

Abstract: A golf ball includes a plurality of dimples on the surface thereof and satisfies the following expression (1): PS7/S/H×100?6.25 (mm?1)??(1), wherein H is a deformation amount, which is expressed by a compressive deformation amount of the golf ball; S is a virtual plane area, which is a surface area of the golf ball determined supposing that no dimple exists on the surface of the golf ball; and PS7 is a pressurized area, which is an area of the golf ball contacting a plane when a load of 6864 N is applied to the golf ball. The bottom of the dimple includes a center protruding portion with a curved shape protruding toward an outside of the golf ball.

Abstract: An object of the present invention is to provide a golf ball excellent in durability. The present invention provides a golf ball comprising a constituent member containing a crosslinked rubber component and a polyrotaxane component, wherein the polyrotaxane has a cyclodextrin, a linear molecule piercing through the cyclic structure of the cyclodextrin, and blocking groups located at both terminals of the linear molecule to prevent disassociation of the cyclodextrin, and at least a part of hydroxyl groups of the cyclodextrin is modified with a caprolactone chain via —O—C3H6—O— group.

Abstract: Disclosed herein are polyurethane golf ball compositions. The compositions are prepared by adding a UV absorber to a polyol prior to reacting the polyol with an isocyanate to form a prepolymer, which is then reacted with a curing agent to form the polyurethane.

Abstract: Tubular projectile devices are disclosed herein. An exemplary tubular projectile device includes a spheroid frame having a long axis and a short axis. Further, the exemplary tubular projectile device includes a tubular medial section coupled with the spheroid frame; a first bicone comprising an exterior first cone congruent with an interior first cone, the first bicone being terminal along the long axis of the spheroid frame and coupled with the spheroid frame; and a second bicone comprising an exterior second cone congruent with an interior second cone, the second bicone being terminal along the long axis of the spheroid frame and coupled with the spheroid frame. The exemplary tubular projectile device may be a football.