Abstract: An abdominal exercise device has a kneeling pad and a roller. The kneeling pad includes a top surface and two spaced apart kneeling recesses. The kneeling recesses are formed in the top surface of the kneeling pad. The roller is positioned movably relative to the kneeling pad when in use and includes a bracket, a left handle, a right handle, a front wheel and two rear wheels. The left and right handles are attached to a middle of the bracket. The front wheel is mounted on a front of the bracket. The rear wheels are mounted on a rear of the bracket. The kneeling recesses are ergonomically designed to correspond to contours of the human knees, thereby providing a comfortable support for a user's knees. The three wheels ensure that the roller has good balanced performance such that the user can steadily operate the roller.

Abstract: A system for performing proprioceptive neuromuscular facilitation (“PNF”) stretching. The system includes a harness portion comprising a harness strap with movably attached buckle portions and a hook receptacle surrounding the harness strap to support the harness strap when the hook receptacle is suspended. The harness strap includes a mini-strap with buckle portions extending in parallel with the harness strap. The harness strap buckle portions mate with the mini-strap buckle portions to form a double loop harness configuration, and alternatively, combine with a single loop enabler to form a single loop harness configuration. An attachment strap is configured for attachment to a fixing structure by a movably attached hooking mechanism, which varies the distance between the attaching end of the attachment strap and the hooking mechanism. The harness portion attaches to the attachment strap attached to the fixing structure to provide a user with a body support while in un-balanced positions.

Abstract: A balance board adapted for riding rail-to-rail, preferably so that at least a portion of a rider's feet will be placed on the board over the elongated roller. The balance board includes an elongated, planar board having a length that exceeds a width. The balance board further includes two pair of stops mounted to an underside of the board, each pair of stops being mounted near opposite ends of the board, and each stop of the pair of stops being mounted near opposite sides of the board. The balance board further includes a traction region between each stop of each pair of stop.

Abstract: The present disclosure relates to a tool gripper chain bendable in two directions that has a chain assembly that includes: gripper blocks that each have a first tooth at the center of a curved groove; first and second gripper assemblies that have first and second gripper members rotatably mounted on the rear of gripper blocks and grip a tool; first and second outer links that are formed in an arc shape; first and second inner links that are formed in an arc shape and disposed zigzag with respect to first and second outer links between first outer link and second outer link; and first and second collars that are disposed between first inner link and second inner link, in which first gripper assembly is disposed in front of second outer link, second gripper assembly is disposed ahead of second inner ink, and a first shaft hole of first gripper assembly and second shaft hole of second gripper assembly are coaxially arranged, such that first and second gripper assemblies are coupled by a first shaft or a second s

Abstract: A roller includes a shaft including reinforcing fiber and a binder resin; and an elastic body surrounding an outer surface of the shaft, wherein an average length to average diameter ratio (L/D) of the reinforcing fiber is from about 15,000:1 to about 50,000:1.

Abstract: A method of forming a valve bag suitable for filling with, for example, powder, grain, cement, animal foodstuffs, via a chute tube inserted into the valve, including forming a combined web from two webs of material, including steps of forming the combined web into a plurality of bag sections, sealing the bag sections at one side such that a valve portion is defined, separating the two webs and moving them outwardly until the bag sections are turned inside, and sealing the two webs to form a valve bag having an strong, effective seal and a valve portion for filling.

Abstract: The present invention provides a restored winding core and a method for manufacturing the same, wherein at least one discarded winding core is first collected. At least one of the extremities of the discarded winding core is internally ground on a predetermined grinding distance to remove the crimping portion and provide a ground portion thereon. The ground portion defines a female joint socket extending at the corresponding extremity of the discarded winding core for providing a machined core extremity. The method also comprises the step of providing at least one hollow insert tube diametrically snugly fitting into the female joint socket. The at least one insert tube is inserted inside the corresponding female joint socket for providing a restored core extremity. The present invention thus allows to restore the damaged extremities of a winding core which can then be reused as a new winding core of the same length.

Abstract: A method and apparatus for forming patterns on sheet material are disclosed. The method comprises a continuous lateral stretch process for producing zero- or near zero-curvature structures. In a preferred embodiment, the method comprises pre-gathering the sheet material in the lateral direction to form longitudinal corrugated folds and then feeding the corrugated material through one or more sets of oscillating formers, preferably articulating discs, to impart folding in the lateral direction. Optionally, the sheet material may be fed through one or more sets of patterned rollers.

Abstract: A vertical centrifugal separator includes a casing, a bowl that is rotatably housed in the casing and provided to separate a solution to be processed which is supplied to an interior of the bowl into a liquid and a solid by an action of centrifugal force and discharge the liquid and the solid, and a discharge assembly that is rotatably housed in the bowl and provided to discharge the solid in the bowl. The bowl and the discharge assembly each have an engagement portion that is engaged or disengaged when the bowl and the discharge assembly are moved relative to each other in an axial direction and a position adjustment mechanism for adjusting a phase between the discharge assembly and the bowl relative to a rotation axis, for example, at a single relative position.

Abstract: Containers and methods for disposing unused pharmaceutical product are disclosed. Each container (100, 200, 300) may include a container body (104, 204, 304) with an internal chamber (116, 216, 316) for storing pharmaceutical product, along with a cover (124, 224, 324) for selectively limiting access to the chamber (116, 216, 316). An encapsulation component (128, 228, 328) may be selectively disposable within the chamber (116, 216, 316), and may be operable to encapsulate the pharmaceutical product within the container (100, 200, 300). For instance, the encapsulation component (128, 228, 328) may melt and/or flow into contact with the pharmaceutical product and thereafter solidify to encapsulate the pharmaceutical product. The encapsulation component (128, 228, 328) may melt and thereafter solidify between the cover (124, 224, 324) and shell (104, 204, 304) to limit removal of the cover (124, 224, 324) from the shell (104, 204, 304).

Abstract: Delivery systems and methods for delivering riboflavin (R/F) and UVA irradiation to the sclera are disclosed. The R/F is delivered and then activated with UVA irradiation through the use of LEDs or optical fibers, thereby causing cross-linking of the collagen tissue. Delivery systems include implantable structures which provide surfaces that conform to the sclera. The delivery systems include various types of structures for delivery of R/F onto the sclera surface. Additionally, the delivery systems include UVA sources which provide irradiation of R/F in sclera collagen tissue.

Abstract: A method is described for decreasing activity of at least one sympathetic nerve, nerve fiber or neuron innervating at least one blood vessel in the pulmonary vasculature of a patient to ameliorate pulmonary hypertension. In one embodiment, the method may involve advancing an intravascular treatment device to a target location in a target blood vessel within the pulmonary vasculature of the patient and using the treatment device to decrease activity of at least one sympathetic nerve, nerve fiber or neuron innervating the target blood vessel at or near the target location to ameliorate pulmonary hypertension.

Abstract: A method and system enabling delivery of a therapy type is provided. The method includes receiving a value of a parameter measured by physical sensors while a mammal is in contact with a first subset of the physical sensors. A second subset of the physical sensors, whose received value differs from a predetermined reference value of an environmental parameter, is determined. A physical part subset of the second subset, corresponding to a specified body part, is determined by utilizing the second subset and virtual data for identifying virtual sensors spatially distributed to map a space occupied by the mammal's body parts. In response, a therapy device positioned in sufficiently close proximity to the specified body part to effectively deliver the specified therapy type to the specified body part, is determined and a control signal is generated and transmitted to the associated therapy device.

Abstract: Energy emitting systems are provided which include an adjustable conductive coil configured to generate a magnetic or electromagnetic field focused on a target nerve. The coil includes a central aperture which may be adjustable between a first configuration and a second configuration having a radius greater than the radius of the first configuration. The adjustable or movable nature of the coil allows the conductive coil to conform to, accommodate, or be positioned on a particular anatomical structure of a patient to position the coil in proximity to the underlying target nerve. In certain embodiments, methods of magnetic induction therapy are provided which include positioning a conductive coil relative to a portion of a patient's body by adjusting the central aperture of the coil such that the coil may conform to, accommodate or be positioned on the portion of the patient's body in proximity to the underlying target nerve.

Abstract: A device and a method of applying the device for the treatment of obesity or overweight in mammals, especially humans refers to a suitable substrate to be worn at the body of the patient and includes a thyroid stimulating pulsating magnetic field, whereby the magnetic field can be controlled and programmed as to the duration, frequency and pulsation of the magnetic field.

Abstract: An implantable device for improving the pump function of the heart of a human patient by applying an external force on the heart muscle is provided. The device comprises at least one pump device having a pump. The pump comprising: a piston adapted for reciprocating movement, an operating device for operating the piston, a heart contacting organ. The movement of the piston assists the pump function of the heart through said heart contacting organ.

Abstract: A circulatory assist system is disclosed, the system including an implantable electrical device having an electric motor, an implantable controller connected to the implantable electrical device, and an implantable power source connected to the controller for supplying power to the controller. The controller is attachable to a first side of a percutaneous connector. A second side of the percutaneous connector, opposite to the first side, allows external connectivity to said controller.

Abstract: In some embodiments of the present invention, apparatus is provided, including a sensing electrode configured to be implanted at a non-cardiac site in a vicinity of an aorta of a subject and to detect an electrical parameter of the aorta, and a control unit configured to receive the detected parameter and to generate an output in response to the detected parameter. Additional embodiments are also described.

Abstract: Methods and devices treat non-stuttering pathologies having impaired or decreased communication skills by administering a frequency altered auditory feedback signal to a subject having a non-stuttering pathology while the subject is speaking or talking to thereby improve the subject's communication skills.

Abstract: Devices and methods are provided for drug delivery. The device may include a housing configured for intralumenal deployment into a human or animal subject and first and second reservoirs within the housing, each reservoir having an actuation end, an opposed release end, and a plug moveable from the actuation end toward the release end. First and second drug formulations may be contained in the first and second reservoirs, respectively. The device may also include one or more actuation systems configured to drive the first and second plugs so as to drive the first and second drug formulations from the first and second reservoirs. The housing may include a porous membrane sidewall in fluid communication with the release ends of the first and second reservoirs, the porous membrane sidewall being configured to distribute the first and second drug formulations driven from the first and second reservoirs.

Abstract: A cardiac constraint device comprising a jacket of biological compatible material and an adjustment member. The jacket is adapted to be secured to the heart to snugly conform to an external geometry of the heart and assume a maximum adjusted volume to constrain circumferential expansion of the heart beyond the maximum adjusted volume during diastole and to permit unimpeded contraction of the heart during systole. The adjustment mechanism is configured to alter the internal volume defined by the jacket after the jacket is secured to the heart. The invention also provides a method for treating cardiac disease.

Abstract: A decorative glass dildo comprising a solid, high density heat-resistant glass outer portion, a coated decorative inner portion, a sealing ring attached to the inner portion, an electrical conductive strip attached to the inner portion, and an end portion mechanically attached to the inner portion of the glass dildo.

Abstract: A penile prosthesis implantation device includes a barrel having a bore, an obturator and a needle clamp. The obturator has a distal end that is received within the bore of the barrel and is configured to slide along a longitudinal axis of the bore relative to the barrel. The needle clamp is at the distal end of the obturator and includes opposing pinching members that are displaced from an interior wall of the bore when the needle clamp is retracted within the bore, and a receptacle between the pinching members configured to receive a thread attachment end of a needle and hold the end of the needle through an interference fit with the pinching surfaces.

Abstract: The present invention is directed to an articulate minimally invasive surgical endoscope with a flexible wrist having at least one degree of freedom. When used with a surgical robot having a plurality of robot arms, the endoscope can be used with any of the plurality of arms thereby allowing the use a universal arm design. The endoscope in accordance to the present invention is made more intuitive a to a user by attaching a reference frame used for controlling the at least one degree of freedom motion to the flexible wrist for wrist motion associated with the at least one degree of freedom. The endoscope in accordance to the present invention attenuates undesirable motion at its back/proximal end by acquiring the image of the object in association with the at least one degree of freedom based on a reference frame rotating around a point of rotation located proximal to the flexible wrist.

Abstract: In one embodiment, an endoscopic camera for a robotic surgical system includes a stereo camera module mounted to a robotic arm of a patient side cart. The optical and electro-optic components of the camera module are hermetically sealed within a first housing. Signals from an electro-optic component travel through traces in a ceramic substrate forming one side of the hermetically sealed first housing. A second housing surrounds the first housing and optical fibers are dispersed between the housings to provide lighting in a body cavity. The camera module may be sterilized by an autoclave.

Abstract: An articulated device may include a first steerable multi-linked mechanism and a second steerable multi-linked mechanism. The second steerable multi-linked mechanism may include a first link, a plurality of intermediate links and a second link movably coupled to a second one of the intermediate links. A first one of the intermediate links may be movably coupled to the first link. The articulated device may include a camera located within at least a portion of the second link and a protective shield connected to a distal end of the second link. The protective shield may surround at least a portion of the camera.

Abstract: An illumination system includes an arthroscope, endoscope or other suitable surgical tool and an attachable cannula comprising a transparent or semi-transparent material capable of carrying light from the proximal end of the cannula to the distal end of the cannula, thereby illuminating the surgical field. The surgical field is thus illuminated through components that do not occupy space that may otherwise be used for the optics of the arthroscope. The arthroscopic illumination system further comprises one or more illumination sources disposed at the proximal end of the cannula. The illumination source may be optically coupled with the cannula at the hub or other appropriate location. The cannula comprises a sterilizable polymer which functions as a waveguide. A waveguide is a material medium that confines and guides light. When in use, the light source connected to the hub provides light which may be guided to the distal end of the cannula or any other suitable location.

Abstract: Various devices and methods are provided with respect to inserting multiple surgical instruments through a single surgical access device. A medical device including a flexible tissue retractor a releasable insert having multiple instrument openings, and a member such as a sleeve is disclosed. The insert can be in the form of an insert assembly including multiple components. The sleeve can support the insert with respect to the retractor such that the insert and sleeve can be removed together with the retractor remaining in the incision. A method of using the insert is also described.

Abstract: The present invention relates to a surgical tool guide, which is easily installed and separated to reduce operating time, and furthermore surgical instruments are not separated from the abdominal walls or gas does not leak to stably perform the surgical operation. In addition, the present invention relates to a protection cap for a surgical instrument guide, which is interlocked together with surgical instruments to maintain a seal even though the surgical instruments for the operation are variously moved, thereby efficiently preventing the leakage of gas. Therefore, since it is unnecessary to inject gas again during the operation, the surgical operation can be smoothly performed.

Abstract: A surgical access system for providing access to a surgical site in a patient includes a surgical access device defining a port and a light emitter coupled to the surgical access device for illuminating the port. The light emitter preferably comprises an elongated shaft having a light transmitting element housed therein, which emits light transmitted to the elongated shaft from a light source. The elongated shaft is configured to be inserted in an elongated channel in the access device. The elongated channel has or forms a window for transmitting light emitted by the light emitter into the interior of the access device.

Abstract: A system and method for providing computerized, knowledge-based medical diagnostic and treatment advice. The medical advice is provided to the general public over networks, such as a telephone network or a computer network. The invention also includes a stand-alone embodiment that may utilize occasional connectivity to a central computer by use of a network, such as the Internet. New authoring languages, interactive voice response and speech recognition are used to enable expert and general practitioner knowledge to be encoded for access by the public. “Meta” functions for time-density analysis of a number of factors regarding the number of medical complaints per unit of time are an integral part of the system. A re-enter feature monitors the user's changing condition over time. A symptom severity analysis helps to respond to the changing conditions. System sensitivity factors may be changed at a global level or other levels to adjust the system advice as necessary.

Abstract: A vital signs monitor system is integrated with personal protective equipment (“PPE”) so that upon wearing the PPE, the monitor is placed in an operational position to monitor a vital sign. In one embodiment, the vital signs sensor comprises a thermal sensor located at a mouth guard to automatically make operational contact with tissue under the tongue when the mouth guard is worn. A second vital signs monitor comprising reflective pulse oximetry devices senses oxygen saturation and heart rate. Vital signs data are communicated to an RF module located in an associated helmet for transmission to a remote location. A gateway at that remote location receives the transmitted vital signs data and forwards that data to a data collection, organization, and access system that is programmed to make the vital signs data available over the Internet.

Abstract: A system and method tests the gastric valve and urethral sphincter in a patient. A contrast agent is administered into the esophagus of a patient followed by inducing an involuntary reflex cough epoch within the patient to isolate the gastric valve from the lower esophageal sphincter (LES) and isolate the external urethral sphincter from the internal urethral sphincter. An imaging sensor detects the flow of the contrast agent during the involuntary reflex cough epoch and determines whether stomach reflux occurred indicative of a malfunctioning gastric valve. A determination is made if urine leakage occurs indicative of stress urinary incontinence (SUI).

Abstract: A device to block emesis and/or reflux includes a tube insertable into the esophagus. A valve is carried by the tube and includes a flexible sheath having an upper edge secured onto the tube and an unsecured lower circumferential edge and configured such that upon contact with emesis and/or reflux from the stomach, the flexible sheath opens in a concave configuration towards the stomach and the unsecured lower circumferential edge engages the esophageal wall and blocks emesis and/or reflux from the stomach passing into the esophagus past the valve.

Abstract: A device blocks emesis and/or reflex and includes a tube insertable into the esophagus. The tube includes an inflation lumen. A valve is carried by the tube and includes a flexible sheath having an upper edge secured onto the tube and a lower circumferential edge. An inflatable balloon is associated with the flexible sheath and in communication with the inflation lumen. Upon inflation of the balloon, the flexible sheath opens in a concave configuration towards the stomach and the unsecured lower circumferential edge engages the esophageal wall and blocks emesis and/or reflux from the stomach passing into the esophagus past the valve.

Abstract: A nasogastric/orogastric (Ng/Og) device includes a main lumen configured for at least one of gastric decompression, enteral feeding and enteral medication administration. An expandable esophageal cuff is carried by the device body and configured in a normally expanded position such that when inserted within the esophagus, the esophageal cuff conforms to the interior surface of the esophagus and emesis and/or reflux is blocked from passing out of the stomach and past the esophageal cuff. A vacuum lumen is carried by the device body and connected to the expandable esophageal cuff. When vacuum is applied, the esophageal cuff is contracted against the device body to permit the device to be inserted and placed within the esophagus. When the vacuum is released, the esophageal cuff expands against the interior surface of the esophagus.

Abstract: A tonometer includes a pair of arms pivotally connected at proximal ends thereof, one arm having a contact member at a distal end. Mounted to the one arm and in contact with the contact member is a pressure transducer providing an electrical signal corresponding to the pressure applied to the contact member. A control circuit responds to the signal to indicate on a visual display the intraocular pressure.

Abstract: Tissue Pulsatility Imaging (TPI) is an ultrasonic technique developed to measure tissue displacement or strain in the brain due to blood flow over the cardiac and respiratory cycles. Such measurements can be used to facilitate the mapping of brain function as well as to monitor cerebral vasoreactivity. Significantly, because tissue scatters ultrasound to a greater extend than does blood, using ultrasound to measure tissue displacement or strain in the brain is easier to implement than using ultrasound to measure blood flow in the brain. Significantly, transcranial Doppler sonography (TCD) has been used to measure blood flow in the brain to map brain function and monitor cerebral vasoreactivity; however, TCD can only acquire data through the three acoustic windows in the skull, limiting the usefulness of TCD. TPI is not so limited.

Abstract: There is provided an ultrasound image picking-up device that can correct a positional shift from a reference image before therapy even with insufficient clarity of an ultrasound image.

Abstract: An imaging part acquires a plurality of ultrasound image data by sequentially imaging the subject with ultrasound waves. A display controller causes a display to display, side by side, a plurality of ultrasound images based on the plurality of ultrasound image data acquired by the imaging part. Moreover, the display controller causes the display to display measurement markers for obtaining quantitative information of tissues shown in the ultrasound images in a state superimposed in relatively the same positions on the plurality of ultrasound images.

Abstract: A biometric monitoring device is used to determine a user's heart rate by using a heartbeat waveform sensor and a motion detecting sensor. In some embodiments, the device collects collecting concurrent output data from the heartbeat waveform sensor and output data from the motion detecting sensor, detects a periodic component of the output data from the motion detecting sensor, and uses the periodic component of the output data from the motion detecting sensor to remove a corresponding periodic component from the output data from the heartbeat waveform sensor. From this result, the device may determine and present the user's heart rate.

Abstract: A method for tracking cardiac conditions is disclosed. An electrical signal from a patient's heart is sensed. A heart signal parameter value and an associated heart rate value are computed from the electrical signal. Based on the heart rate value, one of a plurality of histograms stored in a histogram memory is updated with the heart signal parameter value. After a data collection time period has elapsed, a statistical value of the heart signal parameter is computed from the selected histogram. A detection threshold for abnormal values of the heart signal parameter is then computed based on the statistical value.

Abstract: Disclosed is a system and method for monitoring the breath chemistry of a patient's breath using a specially designed self-condensing sensor module mounted in a mask, nasal cannula, headband with boom apparatus, or similar device for directing the patients' breath towards the self-condensing sensor. Monitoring of a patient's breath pH provided by the miniaturized self-condensing pH sensor provides for real-time monitoring of patient airway pH values. The specially designed self-condensing sensor module incorporates a data transfer means, e.g. direct wiring or by providing a transmitter with an antenna for wireless transferring of the pH data to a processing receiver. The self-condensing pH sensor comprises a multi-tubular design with the outer tubular member housing a silver chloride reference element, an ion conducting path, and an antimony sensor plug isolated in an inner tubular member that is co-linearly or coaxially configured with the outer tubular member.

Abstract: An apparatus (2) for use in diagnosing and/or treating a neurological disorder is disclosed. The apparatus comprises a sensor device (4) designed to resemble a pen to provide a first signal containing first data representing a force applied by at least one finger of the subject, an integrated writable surface (10) to (i) provide at least one second signal containing second data representing a position of the sensor device (4) relative to the writable surface (10) and/or (ii) provide at least one third signal containing third data representing an engaging force of the sensor device on the writable surface, and a camera (20) to provide at least one fourth signal containing fourth data representing a position of at least one part of an arm of the subject holding the sensor device (4).

Abstract: An implantable medical device having a flexible diaphragm is provided with a housing including a shell and an outer layer. The flexible diaphragm extends along the shell. The outer layer has an outer surface and an inner surface. An adhesive coating is applied between the diaphragm and the inner surface of the outer layer. The outer layer includes a recess along the diaphragm for receiving the adhesive.

Abstract: A biopsy device and method are provided for obtaining a tissue sample, such as a breast tissue biopsy sample. The biopsy device includes a disposable probe assembly with an outer cannula having a distal piercing tip, a cutter lumen, and a cutter tube that rotates and translates past a side aperture in the outer cannula to sever a tissue sample. The biopsy device also includes a reusable hand piece with an integral motor and power source to make a convenient, untethered control for use with ultrasonic imaging. External vacuum holes along the outer cannula (probe) that communicate with a vacuum and cutter lumen withdraw bodily fluids while a hemostatic disk-shaped ring pad around the probe applies compression to an external hole in the skin and absorbs fluids.

Abstract: A device and method for collecting a urine sample from a neonate is provided. The device is attached to the neonate shortly after birth and removed after the neonate produces a urine sample. An interior shell and an exterior shell form the device, and an absorbent material is located inside the interior shell to absorb the urine sample. The interior shell and the exterior shell are connected by a hinge and are initially in a nesting position, with the exterior shell on top of the interior shell. After the urine sample is absorbed by the absorbent material, the exterior shell is rotated around an axis defined by the hinge to contact and compress the absorbent material to release the urine sample for collection.

Abstract: A coupling wire guide for intracorporeal procedures that may be coupled to a previously introduced wire guide, thereby permitting introduction of the coupling wire guide separately and identically in a manner that is both reliable as well as traceable. One embodiment of the wire guide includes a main body having a distal end and a tip portion connected to the distal end of the main body. The tip portion defines an axial passageway having a distal opening and a proximal opening, the passageway being sized to receive a second wire guide therein. The tip portion includes a linking member connected to the distal end of the main body to provide a secure connection between the distal end of the main body and the tip portion.

Abstract: A device for determining a physical parameter of a tissue opening is provided. The device includes an expandable member which is designed for positioning within a tissue opening such as a valve annulus. The expandable member is capable of expanding while applying an inward radial force indicative of a diameter thereof. When the expandable member is positioned within the tissue opening and expanded, an increase in the inward radial force induced by contact between the expandable member and tissue surrounding the opening can be utilized to derive information relating to the physical parameter of the tissue opening.

Abstract: The present invention relates to embodiments which enable repetitive measurement and monitoring of the load applied to an apparatus, in a system, and/or by a method which may exceed a predetermined threshold of weight. Specifically, the present invention relates to weight monitoring apparatus, locomotion monitoring apparatus, a gait-response apparatus, a weight monitoring system, and a therapeutic load monitoring method.