Abstract: An occlusion device includes first and second crossing frame elements each of annular ring-shape, as well as first and second annular support elements connected to respective extremities of the crossing frame elements. The frame and support elements are provided with covers made of a substantially impervious material. The occluder may include a covering sleeve of stretchable material. The occluder substantially stops or reduces the flow of blood therethrough, creating blood statis and subsequent occlusion by clot formation within the occluder. The structure of the frame elements ensures good edge sealing and enhanced fixation of the occluder in a vessel as blood pressure impinges upon the covers of the occluder.

Abstract: The present invention relates to a fluid applicator apparatus and methods of using the apparatus. In particular, the present invention relates to an apparatus for storing and dispensing solutions (e.g., fluid solutions of any kind) (e.g., liquid medicaments and/or sterilization solutions) to a surface of a subject.

Abstract: Embodiments of the invention provide swallowable devices, preparations and methods for delivering drugs and other therapeutic agents within the GI tract. Many embodiments provide a swallowable device for delivering the agents. Particular embodiments provide a swallowable device such as a capsule for delivering drugs into the intestinal wall or other GI lumen. Embodiments also provide various drug preparations that are configured to be contained within the capsule, advanced from the capsule into the intestinal wall and degrade to release the drug into the bloodstream to produce a therapeutic effect. The preparation can be operably coupled to delivery means having a first configuration where the preparation is contained in the capsule and a second configuration where the preparation is advanced out of the capsule into the intestinal wall. Embodiments of the invention are particularly useful for the delivery of drugs which are poorly absorbed, tolerated and/or degraded within the GI tract.

Abstract: A method for localizing delivery of an agent to a target site in a subject is provided. The method allows accumulation and/or release of the agent at the target site in the subject through the use of an energy source.

Abstract: The invention provides articles of manufacture comprising biocompatible nanostructures comprising nanotubes and nanopores for, e.g., organ, tissue and/or cell growth, e.g., for bone, kidney or liver growth, and uses thereof, e.g., for in vitro testing, in vivo implants, including their use in making and using artificial organs, and related therapeutics. The invention provides lock-in nanostructures comprising a plurality of nanopores or nanotubes, wherein the nanopore or nanotube entrance has a smaller diameter or size than the rest (the interior) of the nanopore or nanotube. The invention also provides dual structured biomaterial comprising micro- or macro-pores and nanopores. The invention provides biomaterials having a surface comprising a plurality of enlarged diameter nanopores and/or nanotubes.

Abstract: Technologies and implementations for a defibrillator electrode having communicative capabilities are generally disclosed.

Abstract: Various fixation techniques for implantable medical device (IMDs) are described. In one example, an assembly comprises an IMD; and a set of active fixation tines attached to the IMD. The active fixation tines in the set are deployable from a spring-loaded position in which distal ends of the active fixation tines point away from the IMD to a hooked position in which the active fixation tines bend back towards the IMD. The active fixation tines are configured to secure the IMD to a patient tissue when deployed while the distal ends of the active fixation tines are positioned adjacent to the patient tissue.

Abstract: A three-dimensional neural probe electrode array system is described. Planar probes are microfabricated and electrically connected to flexible micro-machined ribbon cables using a rivet bonding technique. The distal end of each cable is connected to a probe with the proximal end of the cable being customized for connection to a printed circuit board. Final assembly consists of combining multiple such assemblies into a single structure. Each of the two-dimensional neural probe arrays is positioned into a micro-machined platform that provides mechanical support and alignment for each array. Lastly, a micro-machined cap is placed on top of each neural electrode probe and cable assembly to protect them from damage during shipping and subsequent use. The cap provides a relatively planar surface for attachment of a computer controlled inserter for precise insertion into the tissue.

Abstract: In one embodiment, a neurostimulation lead for stimulating neural tissue of a patient, comprises: a lead body of insulative material; a plurality of electrodes; a plurality of terminals; a plurality of conductors, wherein the plurality of electrodes are electrically coupled to the plurality of terminals through the plurality of conductors; wherein the plurality of conductors are disposed in a helical manner in a repeating pattern of groups of conductors separated by gaps along a substantial length of the lead body, each gap being larger than an inter-conductor pitch within the groups of conductors; wherein the insulative material is a compliant material permitting elongation of the lead at low stretching forces and the insulative material of the lead body is fused through a substantial volume of the lead body and along a substantial length of the lead body.

Abstract: A system for use in stimulating bone growth, tissue healing, and/or pain control is described. The system includes a screw, a battery, a controller, and means for connecting the battery such that current is routed from the battery through the screw and thence to a target area of interest requiring treatment. The screw includes an elongate shaft having a length extending between opposite ends. The shaft has an insulating coating extending along at least a portion of the length. The thickness of the insulating coating at various portions of the shaft is modulated to optimally direct current to a target area of interest requiring treatment. The controller adjusts the duty cycle of the current flow over the treatment period.

Abstract: A device for positioning an electrode in tissue includes: a lead body having a distal portion; an electrode array coupled to the lead distal portion; an anchoring element having an anchor tip and being operable in a first configuration in which the anchor tip is retracted within the lead and in a second configuration in which the anchor tip is extended outside the lead and configured to fixate within the tissue; and a displacement mechanism that is actuated to bias the electrode array or the anchoring element toward the tissue. A method for positioning an electrode in tissue includes: navigating, to the tissue, a lead with an electrode array, an anchoring element with a distal anchor tip, and a displacement mechanism; biasing the electrode array and anchoring element towards the tissue with the displacement mechanism; and deploying the anchoring element, and verifying fixation of the anchor tip within the tissue.

Abstract: An engagement subassembly of a catheter, for retrieving an implanted medical device, may include at least three segments or, alternately, capture members being spring biased outward from a longitudinal axis of the subassembly, wherein a device receptacle of the catheter forces the capture members/segments, against the spring bias thereof, toward the axis. Each capture member includes a spring-biased wire and a grip, which is located between proximal and distal portions of the corresponding wire, and which is configured to interlock within a gap between a device attachment feature and housing; a length of each wire distal portion may be approximately equal to that of the device housing. An interlocking edge of each segment interlocks within the gap between the attachment feature and housing, when a distal-facing surface of each segment, which tapers outward from the axis in a distal direction, comes into confronting engagement with the device housing.

Abstract: Example implantable cardiac stimulation devices, pulse generators, and methods providing enhanced cardiac pacing energy are disclosed herein. In an example, an implantable cardiac stimulation device may include a pulse generator having a pacing output node providing cardiac pacing pulses to be applied to a heart of a patient. The pulse generator may include a pulse voltage regulator that receives a pacing signal and generates cardiac pacing pulses at an output of the pulse voltage regulator according to the pacing signal. The pulse voltage regulator may receive a supply voltage to generate cardiac pacing pulses at the supply voltage, gated by the pacing signal.

Abstract: A system for retaining a magnet in a cochlear implant, comprising a retainer embedded within an encapsulant of the cochlear implant, and a magnet case engaged with the retainer. A retainer for retaining a magnet within a cochlear implant comprising a number of first fasteners that couple with a number of corresponding second fasteners of a magnet case hermetically sealing the magnet, and a number of supports embedded within an encapsulant of the cochlear implant.

Abstract: A system and method for conditioning surfaces of a body in vivo includes providing an electrical energy source, coupling the electric energy source to the surface, and delivering electropositive current from the electrical energy source to the surface so as to generate a sub-threshold current density on the surface. In preferred embodiments, the sub-threshold electropositive current density is between about 0.001 and about 1.0 mA/cm2.

Abstract: Improved neuromodulation control of neurological abnormalities associated with effector organs in vertebrate beings using direct current stimulation for modulating spinal cord excitability, having a peripheral-current supplying component for providing direct current peripheral nerve stimulation and a spinal-current supplying component providing direct current for spinal stimulation, and a controller managing such functions.

Abstract: Iontophoretically administering a cosmetic agent requires an active electrode and a return electrode secured to the skin (150). The active electrode includes a flexible biocompatible substrate (20, 170) having a therapeutic face (106, 206) configured for disposition toward the skin (150) and an exterior periphery (32, 182) shaped to facilitate conformance of the substrate (20, 170) to the skin (150) over an intended treatment region. A flexible electrically conductive layer (110, 210) is disposed on the therapeutic face (106, 206). The side of the conductive layer (110, 210) opposite from the substrate (20, 170) defines a driving face (120, 220) to which is affixed an electrically conductive adhesive matrix (82, 192) comprised of a material capable of repeatedly releasably securing the active electrode to the skin (150) through an applied solution (156, 158) of the cosmetic agent.

Abstract: Presented herein are techniques for determining an arrangement of complex stimulation channels to optimally distribute sensory information across the channels of a multi-channel tissue-stimulating prosthesis. A tissue-stimulating prosthesis may initially be associated with a set of complex stimulation channels. A stimulation efficiency is determined for each complex stimulation channel within the set of complex stimulation channels. A first complex stimulation channel from the set of complex stimulation channels that has an associated stimulation efficiency that is below a stimulation efficiency limit is identified. The first complex stimulation channel is combined with an adjacent/neighboring complex stimulation channel to create a combined complex stimulation channel. The combined complex stimulation channel replaces both the first complex stimulation channel and the adjacent complex stimulation channel within the set of complex stimulation channels.

Abstract: A cochlear implant is disclosed in an embodiment. The implant includes a signal level detector configured to determine a total signal level of an incoming acoustic signal and a processing unit configured to determine, in accordance with the determined total signal level, an intermediate knee point for each of a plurality of frequency bands. The implant includes a bandpass filters configured to generate a plurality of band limited audio signals in dependence upon the incoming acoustic signal, each band limited acoustic signal representing an associated audio frequency range relating to at least one electrode of a plurality of an implanted electrode array of the cochlear implant. The implant includes a pulse controller configured to deliver electrical stimulation signals to the plurality of electrodes of the implanted electrode array based on the generated signals and the determined intermediate knee point corresponding to the frequency range.

Abstract: A medical stimulation device such as a cochlear implant configured to provide stimulation of one or more spatially-restricted contiguous portion(s) of the spiral array of auditory nerve fibers in the cochlear (“discrete stimulation regions”). Each discrete stimulation region is defined by the constructive and/or destructive interference of stimulating and limiting signals simultaneously applied to electrode channels of an implanted electrode array, the stimulating and limiting signals being determined based upon transimpedance measurements of intracochlear electrode channels of the implanted electrode array representing specific spread functions of an individual recipient.

Abstract: Example apparatus and methods cause activation of target neural tissue through electrical stimulation of a connected white matter tract to reduce the hyper-excitability of the target neural tissue and thus reduce seizures while preserving memory in humans. Example apparatus and methods apply low frequency (e.g., <10 HZ) electrical stimulation to the forno-dorso-commissure (FDC), detect an electrical signal generated in an area connected to, innervated by, or that can be activated by the FDC in response to the stimulation, and reconfigure the stimulation based on the detected signal and a desired therapeutic effect. The stimulation may be reconfigured to produce an electrical stimulation waveform that will produce the desired therapeutic effect. The desired therapeutic effect may be, for example, reducing hyper-excitability of neural tissue in a target area, reducing hippocampal spikes, reducing seizure odds, or improving recall.

Abstract: A neuromodulation system configured for providing sub-threshold neuromodulation therapy to a patient. The neuromodulation system comprises a neuromodulation lead having at least one electrode configured for being implanted along a spinal cord of a patient, a plurality of electrical terminals configured for being respectively coupled to the at least one electrode, modulation output circuitry configured for delivering sub-threshold modulation energy to active ones of the at least one electrode, and control/processing circuitry configured for selecting a percentage from a plurality of percentages based on a known longitudinal location of the neuromodulation lead relative to the spinal cord, computing an amplitude value as a function of the selected percentage, and controlling the modulation output circuitry to deliver sub-threshold modulation energy to the patient at the computed amplitude value.

Abstract: An implantable medical device comprising a signal generator configured to generate and deliver anti-tachyarrhythmia pacing (ATP) to a heart of a patient and processing circuitry. The processing circuitry is configured to detect an enable event, responsive to detecting the enable event, enable the delivery of ATP by the signal generator, detect a disable event indicating that another implantable medical device cannot be relied upon to deliver an anti-tachyarrhythmia shock, and responsive to detecting the disable event, disable delivery of ATP.

Abstract: Techniques for facilitating communication between an implantable device and an external device are provided. In one example, an implantable device includes a data packet component and a communication component. The data packet component can insert information associated with the implantable device in a defined service field of an advertising data packet. The defined service field can be selected from one or more service fields of the advertising data packet based on the information associated with the implantable device. The communication component can transmit the advertising data packet. The external device can include a scanning component that can scan one or more service fields of the advertising data packet via an advertising communication channel, and a communication component that can establish a communication link with the implantable device in response to a determination that a criterion associated with a service field is satisfied.

Abstract: An external controller/charger system for an implantable medical device is disclosed, in which the external controller/charger system provides automatic switching between telemetry and charging without any manual intervention by the patient. The external controller/charger system includes an external controller which houses a telemetry coil and an external charging coil coupled to the external controller. Normally, a charging session is carried out using the external charging coil, and a telemetry session is carried out using the telemetry coil. However, when a patient requests to carry out telemetry during a charging session, the external charging coil is used instead of the internal telemetry coil.

Abstract: Methods and devices providing multiple criteria for use in arrhythmia identification. Based on inputs including defined rules or parameters, one of a more conservative or more aggressive set of arrhythmia identification parameters can be selected. One or the other of the selectable sets of arrhythmia identification parameters may also be adaptive or modifiable during the use of the system, for example, in response to identified nonsustained episodes, the more conservative set of arrhythmia identification parameters can be modified to become still more conservative. Such modification of arrhythmia identification criteria allows reduced time to therapy when indicated, while allowing more deliberate decisions in other circumstances.

Abstract: Nanoparticle-sized magnetic absorption enhancers (MAEs) exhibiting a controlled response to a magnetic field, including a controlled mechanical response and an inductive thermal response. The MAEs have a magnetic material that exhibits inductive thermal response to the magnetic field and is embedded in a coating, such that the MAE conforms to a particular shape, e.g., hemisphere, dome or shell, chosen to produce the controlled mechanical response. A targeting moiety for specifically binding the MAE to a pathogen target is also provided. The MAEs can be bound by a flexible linker to promote the desired mechanical response, which includes interactions between MAEs that are not bound to any pathogen target for the purpose of forming spheres, spherical shells, or generally spherical dimers to contain the thermal energy produced and to thus reduce collateral healthy tissue damage during hyperthermic treatment.

Abstract: The invention relates to a computer-aided simulation tool, in particular to computer-aided simulation methods, for providing assistance in the planning of thermotherapy, and to suitably configured computer equipment. The thermotherapy comprises hyperthermic treatment of a tumour volume within a volume of a human body. The hyperthermic treatment comprises the application of a magnetic field within a treatment volume by means of a magnetic field applicator. In at least one depot volume, thermal energy can be introduced by means of magnetic, paramagnetic and/or superparamagnetic nanoparticles deposited in the body, by power absorption in the applied magnetic field. Field strength values and optionally calculated temperature distributions are provided for assisting the user in the planning of the thermotherapy.

Abstract: Provided is a biofeedback apparatus using a magnetic stimulator. In the biofeedback apparatus, a tube filled with a non-conductive fluid is disposed between a magnetic stimulator and patient's pelvic floor muscles to measure a change in pressure according to muscle exercise of the pelvic floor muscles, biofeedback is available without insertion of a tool for measurement of a pressure or an EMG (electromyogram) into vagina, urethra, or the like. In the biofeedback apparatus, since driving of the magnetic stimulator and driving of a pressure transducer do not influence each other, a controller can continuously monitor a state of change in pressure of the pelvic floor muscles by using the pressure transducer and, at the same time, can adjust a strength of a magnetic field generated from the magnetic stimulator to an optimal strength according to the monitored state, so that it is possible to maximize the effect of treatment.

Abstract: A skin treatment device for home use is provided herein. The device has enhanced safety features and improved operation efficiency. RF energy is delivered under strict control to a relatively small and well localized volume of the skin, avoiding excessive heating of the skin surface. Surface heating is monitored both by direct temperature measurement and by movement monitoring of the device to ensure proper use and prevent skin overheating and the pain associated therewith.

Abstract: A portable device for insertion of radioactive seeds in percutaneous interstitial brachytherapy applications is described. The device includes: an elongated main body in form of a handpiece; a shielded container of radioactive seeds, received within the main body and having a rotating drum suitable, in use, to release one or more radioactive seeds from the container; means for driving the rotating drum, activatable by an operator and based on lever mechanisms and gears; and means for introducing one or more radioactive seeds in a body site of interest, comprising a substantially wire-shaped pusher. The pusher urges the radioactive seed(s) released from the rotating drum through a cannula unit.

Abstract: An optimization technique for use with radiation therapy planning that combines stochastic optimization techniques such as Particle Swarm Optimization (PSO) with deterministic techniques to solve for optimal and reliable locations for delivery of radiation doses to a targeted tumor while minimizing the radiation dose experienced by the surrounding critical structures such as normal tissues and organs.

Abstract: A radiotherapy equipment control device acquires reference position information for a specific location at a reference time. Furthermore, representative point reference position information is generated from reference position information for a plurality of markers at the reference time, and relative position information up to the reference position information for the specific location is generated. Moreover, representative point position information at another time is generated from the position information for a plurality of markers in a subject at the other time, which differs from the reference time. In addition, position information for the specific location at the other time is generated from the representative point position information and the relative position information.

Abstract: According to one embodiment, A movable part tracking and treatment apparatus, includes: an acquisition unit adapted to acquire a three-dimensional moving image by imaging an inside of a body of a patient; a first projection image generation unit adapted to generate a first projection moving image by projecting the three-dimensional moving image on a two-dimensional surface from a fixed direction, the three-dimensional moving image including a tracing target and an affected part area that are part of internal organs in a displaced state, an affected part image extraction unit adapted to extract the displaced affected part area from the first projection moving image, a tracing target image extraction unit adapted to extract the displaced tracing target from the first projection moving image, a first parameter derivation unit is adapted to derive a first parameter indicative of position information on a beam irradiation point selected from the displaced affected part area in the first projection moving image, an

Abstract: Novel systems and methods for performing treatment (e.g., coloration) of keratinous fibers are disclosed. The methods and systems utilize one or more of a dispensing device which is configured to provide customized composition for treating keratinous fibers (e.g., a coloring composition), optionally formed from tablets; an optical reader, for obtaining sufficient characteristics of the keratinous fibers to make a realistic prediction of the outcome of a treatment (e.g., coloring treatment); a computational units for predicting an outcome of a treatment, optionally being interfaced with the dispensing device and for selecting a customized treatment; and tablet formulations which are useful in preparing customized composition for treating keratinous fibers. Further disclosed are rapidly disintegrating tablets for use in the preparation of compositions for treating keratinous fibers.

Abstract: A breathing airbag device includes a filter airbag, an inner holding stand, a nose holder, a mouth holder, and two elastic straps, wherein the filter airbag is adapted for interacting with and filtering the outside air, the inner holding stand is adapted for supporting and fixing the nose holder and mouth holder, the nose holder is adapted for fittingly supporting the human nose, the mouth holder is adapted for fittingly supporting the human mouth, the inner holding stand is located on the filter airbag, the nose holder and the mouth holder are located on the inner holding stand, and two ends of each of the elastic straps are fixed to an edge position of the nose holder. The present invention has some advantages of good tightness, simple structure and low manufacturing cost.

Abstract: A safety restraint system for use by a worker working in a bucket, including a primary tether line that securely encircles the bucket at a position adjacent to the upper rim thereof; at least a pair of straps connected to the tether line on opposite sides of the bucket; a safety harness or aerial belt adapted to be worn by the worker and having at least a pair of clips attached thereto; and at least a pair of straps that interconnect the harness buckles to the straps on the tether line, thereby interconnecting the harness to the tether line.

Abstract: A fire extinguishing appliance adjustable in foam expansion ratio includes a main body, a spray-head seat connected with the main body, and a guide unit. The main body is provided with an agent chamber received therein with a non-toxic agent, while the guide unit is formed with an inlet, an outlet and an inner wall having a damping piece mounted thereon. Thus, when the non-toxic agent is actuated to pass through the inlet and get into the guide unit, the non-toxic agent will collide with the damping piece and rotate to carry out foaming, able to enhance the foam expansion ratio, the mixing efficiency and the fire extinguishing efficiency of the non-toxic agent.

Abstract: A retractable wall mounted exercise rack system for providing an exercise rack that may be easily and compactly stored when not in use. The retractable wall mounted exercise rack system generally includes one or more brackets attached to a wall, a pair of support members, and a plurality of arms pivotally extending from the brackets and pivotally connecting to the support members. One or more actuators are connected between the brackets and the arms to assist in lifting the structure into a compact retracted position for storage.

Abstract: This invention is a portable exercise system capable of performing multiple exercises for strength and endurance training. The key component is the force generation unit (FGU) which is small and light enough to be suspended during the exercise yet capable of producing a force of 50 lbs. The FGU is programmable allowing it to generate various force vs distance, time or velocity profiles. Different handles, cables and attachments can be connected or used with the FGU perform different exercises. The FGU can charge its battery from the user's energy during use. The FGU can communicate bidirectionally with computers and smart phones for setup and to track the user's performance. Multiple FGUs may be used simultaneously each performing a separate function. The entire system is small enough to fit in a drawer or suitcase. The accompanying software can track the user's performance and function as an automated personal trainer.

Abstract: A glove including a dorsal panel having a finger region. The dorsal panel includes an array of four finger regions and each finger region having at least two weights coupled thereto in a longitudinally spaced relationship to each other. The dorsal panel includes a thumb region spaced and orientated away from the finger region. The thumb region includes a weight coupled thereto. The glove includes a weight coupled to the finger region of the dorsal panel. The weight includes a sealed pocket having heavy grains. The weight is not selectably removable. The glove includes a palmar panel coupled to the dorsal panel and thereby forming a cavity therebetween. The palmar panel includes a slick surface.

Abstract: A versatile weight device for physical fitness routines is disclosed which comprises a plate having a generally H-shaped body having a first leg having an end having a hand grip portion, a second leg having an end having a hand grip portion, a third leg having an end having a hand grip portion, a fourth leg having an end having a hand grip portion, a first handle spanning between the first leg and the fourth leg, a second handle spanning between the second leg and the third leg, a central bore, a first cutout section formed between the first leg, the first handle, and the fourth leg, a second cutout section formed between the first leg and the second leg, a third cutout section formed between the second leg, the second handle, and the third leg, and a fourth cutout section formed between the third leg and the fourth leg.

Abstract: The present invention is new in the art as a multi-configuration upgradable fitness device, which can be configured with none, one or more handle(s) attached around a 0-degree to 360-degree rotational position about a central axis as a best mode and configured for operation into (5) fitness devices not limited to; 1) an exercise ball (no handles), 2) kettle bell (1 handle), 3) medicine ball (2 handles opposite), 4) kettle bell-2 (2 handles near each other) and 5) dumbbell (1 handle to a side), and can be upgraded from 2.5 pounds of weights to 10 pounds and up to 50 pounds in increments of 2.5 pounds from (1) to (20) weights to enable 100 or more configurations of fitness equipment as a best mode that enables over one-hundred fitness exercises with this single device as detailed in the entire disclosure.

Abstract: A portable exercise device allowing a user to perform Pilates type exercises without using traditional, cumbersome equipment. The device uses a pair of wheel assemblies respectively attached to opposing ends of a central shaft. A shaft height can be adjusted from a center of each wheel to a lower point closer to a ground surface. Adjustable cam lockable hand/foot plates are attached to the shaft allowing the user to attach his or her feet to the shaft. Each hand/foot plate includes a rotational plate that allows the hand/foot plate to be positioned at various angles in relation to the shaft. Resistance bands are attached on one side to the shaft and on the opposite side to a resistance source. The resistance source can be the user's own hands or feet, or a retaining strap attached to a lower portion of a door or wall.

Abstract: In order to determine the state of a muscle between a normal non-tired state, a tired state and a passive involuntary tension state, a signal from the muscle is recorded at rest by using an electrode arrangement, where an earth body may prevent the electrodes from picking up signals beyond the extent of the earth body. The frequency content of the signal is determined by spectral analysis, e.g. by computing a moment of the spectrum. A normal frequency content indicates a non-tired muscle state, whereas a low and a high frequency content indicate a tired and a passive involuntary tension muscle state. A mapping is used to improve accuracy of state determination, e.g. with a reference database.

Abstract: Articles of clothing or pieces of athletic equipment include modules, e.g., for sensing physical and/or physiological characteristics associated with use of the clothing or athletic equipment or for performing other functions. Such systems and methods may use physical or other interaction(s) between the module and the article of clothing or piece of athletic equipment for activating and/or deactivating the module and/or sensing devices included with the module, for confirming whether the module and clothing or piece of athletic equipment are authorized for use with one another, and/or for automatic data algorithm selection methods. Additionally, such systems and methods also may use the activation and/or authentication systems for data input to the module. Some examples of such systems and methods may utilize magnets and magnetic sensing systems and/or light (or other radiation) sources and sensing systems for activation, authentication, data input, and/or algorithm selection.

Abstract: Methods and systems are presented for accepting inputs into a treadmill or other exercise equipment to control functions of the treadmill or exercise equipment. An exercise control system can receive gestures and other inputs. The exercise control system can also obtain information about the user of the exercise control system and information about the environment in which the exercise equipment is operating. Based on the input and the other information, the exercise control system can modify or improve the performance or execution of user interface and functions of the exercise equipment. The changes make the user interfaces and/or functions user-friendly and intuitive.

Abstract: An avalanche self-rescue device uses an MEMS accelerometer and possibly a gyroscope in order to determine its orientation relative to the gravitational horizon. Whenever the device is oriented vertically with respect to the gravitational horizon (pointing gravitationally upwardly), a speaker emits a tone to so indicate and possibly a light illuminates in conjunction with the sound output. A different tone and possibly a different light output may be dispensed whenever the accelerometer is not oriented vertically with respect to the gravitational horizon. The device can be a standalone device, incorporated in an item of clothing, safety equipment, etc., or integrated into another electronic device such as a rescue beacon or a cellular phone.

Abstract: The present invention provides a golf ball having an outer surface comprising a plurality of dimples covering greater than 70 percent of the outer surface, wherein at least 20 percent of the dimples incorporate directional surface texturing therein. The directional surface texturing preferably comprises substantially parallel channels or protrusions formed within the dimples.

Abstract: A multi-layer golf ball includes a core, an intermediate layer surrounding the core, and a cover layer surrounding the intermediate layer. The core defines an outer surface that includes a plurality of polygonal land portions substantially aligned on a common sphere, which has a diameter of between 22 mm and 32 mm. The intermediate layer has a radially inward-facing surface that is flush with the outer surface of the core, and has a radial thickness of between 4 mm and 9 mm. The outer surface of the core defines a first set of annular grooves disposed about a first axis, and a second set of annular grooves disposed about a second axis. Each of the first and second set of annular grooves extend radially inward from the common sphere, and the first axis and the second axis are orthogonal.