Abstract: A cover for a prosthetic leg having an outer layer, an inner layer and a foam insert. The outer layer has at least two side edges and an inner surface. The inner layer is permanently attached to the outer layer at the two side edges so as to form a pocket between the inner surface of the outer layer and the inner layer. The foam insert is shaped as a partial human leg, and has an inner cavity and an outer surface. The foam insert is positioned inside the formed pocket such that its inner cavity is located adjacent to the inner layer, its outer surface faces the inner surface of the outer layer, and the entire foam insert is located below the top edge of the inner layer. Further, the cover includes a closing mechanism attached to the two side edges to selectively and securely attach the two side edges to each other.

Abstract: A tubular prosthesis that includes a scaffolding formed by at least one scaffolding filament; a cover; and at least one controlled ingrowth feature constructed and arranged to abut an inner surface of a lumen wall when the prosthesis is implanted in the body lumen. The controlled ingrowth feature may extend inwards or outwards from the prosthesis outer surface. The controlled ingrowth feature may be formed by a scaffolding filament; by a separate filament; by the cover; and combinations thereof.

Abstract: The present embodiments provide a method for delivering a stent comprising providing a stent in a delivery state, where the stent comprises a plurality of interconnected strut segments that enable expansion of the stent from a delivery state to a deployed state. Stacking a frontal surface of a first strut segment at least partially behind a rear surface of a second strut segment in the delivery state. Aligning a sharpened tip of a first barb at least partially circumferentially behind at least one strut segment in the delivery state such that the sharpened tip is not radially exposed. Expanding the stent from the delivery state to a deployed state, wherein the first barb is exposed to a patient in the deployed state.

Abstract: Provided herein is a device comprising: a. stent; b. a plurality of layers on said stent framework to form said device; wherein at least one of said layers comprises a bioabsorbable polymer and at least one of said layers comprises one or more active agents; wherein at least part of the active agent is in crystalline form.

Abstract: A stent includes a plurality of rings which form a tubular scaffold. The rings include an elongation mechanism which allows for further expansion of the stent.

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

Abstract: Stent delivery systems and methods for making and using the same are disclosed. An example stent delivery system may include an inner member having a proximal end. A sleeve may be coupled to the inner member adjacent to the proximal end. A deployment sheath may be disposed about the inner member. A gear rack assembly may be coupled to the deployment sheath. A stent may be disposed between the inner member and the deployment sheath. A handle may be coupled to the inner member and to the deployment sheath. The handle may include an actuation member. The actuation member may be coupled to the gear rack assembly so that actuation of the actuation to member shifts the longitudinal position of the gear rack assembly and the deployment sheath. An engagement mechanism may be coupled to the gear rack assembly. The engagement mechanism may be configured to engage the sleeve of the inner member so that proximal retraction of the gear rack assembly results in proximal retraction of the inner shaft.

Abstract: A gastric balloon includes a scaffold structure, one or more internal inflatable compartments within the scaffold structure, and one or more inflatable bladders formed over the space-filling compartment. The gastric balloon may be deployed transesophageally using a gastroscope and is inflated in situ, preferably using a combination of liquid and gas inflation media.

Abstract: This invention is an expandable intragastric device for reducing food consumption and/or absorption. In an example, this device can be embodied in a plurality of longitudinal expandable members which are arranged in a colonnade configuration to form a restrictive food lumen within a stomach. Pumping a flowable substance between the interiors of these expandable members changes the rate of food flow through the stomach, the capacity of the stomach to hold food, and/or the amount of food absorbed by the body. This offers some of the beneficial effects of gastric sleeve surgery, while also being adjustable and reversible.

Abstract: An intestinal barrier sleeve and corresponding treatments using the sleeve are provided herein. The sleeve generally includes an expanding section coupled to a tubular section at an interface there between. The expanding section is expandable from at least a first collapsed position to at least one expanded position, where the expanding section has a conical shape that when expanded retains the sleeve in the subject gastrointestinal tract. The expanding section may further include a plurality of petal-like elements extending radially from the narrow end of the conical shape and the petal-like elements may be interconnected with a webbing to form the conical shape.

Abstract: A gastrointestinal device for treating obesity includes a three-dimensional porous structure configurable between a compressed pre-deployment configuration to facilitate delivery and an expanded post-deployment configuration. The porous structure includes a first opening at its proximal end and a larger second opening at its distal end. The porous structure also includes a sleeve coupled to its distal end. Optionally, the device further includes a suture at the proximal end of the wire mesh structure to facilitate retrieval and an anti-migration component positioned at the junction of the porous structure with the sleeve. The porous structure is deployed in a patient's stomach such that the anti-migration component sits proximal to the patient's pylorus and prevents migration of the entirety of the device into and through the pylorus. The sleeve extends through the pylorus, into the duodenum and ends in the duodenum or jejunum.

Abstract: A support for an article has a body arranged for length adjustment along a length adjustment axis. A tensioning device is connected to the support and adjustment of the tensioning device shortens or lengthens a length of the support along the length adjustment axis. The body defines at least one opening overlapping at least part of the length adjustment axis such that length adjustment is governed by modification of the size of the at least one opening according to adjustment by the tensioning device.

Abstract: A customizable ankle-foot orthotic for treating foot drop and steppage gate that that enables a wearer to adjust the fit of the orthotic against the wearer's ankle for the purpose of reducing pressure points while ensuring adequate support. The orthotic includes an ankle brace which has a first wing defining a first and second tab which are independently configurable to overlap and selectively couple to the second wing enabling the wearer to customize the fit of the interior face against the wearer's ankle.

Abstract: A splint with at least two restraint portions is used for reducing a bone fracture in a body part that has a first surface and a second surface, where the bone fracture has produced at least a first bone fragment and a second bone fragment. The splint includes a first restraint portion configured to apply pressure directly to the first surface of the body part and a second restraint portion configured to apply pressure directly to the second surface. The first and second restraint portions thereby apply pressure to the first and second bone fragments, respectively. The orientation of the first restraint portion and the second restraint portion can be adjusted to align the first bone fragment and the second bone fragment in a desired orientation that substantially corresponds to an orientation for the first bone fragment and the second bone fragment in a non-fractured bone.

Abstract: A multilayer orthotic/orthosis has a cover layer, a shell layer and a posting layer. The shell layer is formed of a thermoplastic having a moldable temperature. The rigidity of the shell layer, and in particular the rigidity of the thermoplastic is chosen to be of a magnitude to support the portion of the individual at temperatures below the moldable temperature. The shell layer, preferably the thermoplastic, has a flexibility above the moldable temperature to mold the shell layer into a shape to support the portion of the individual. The shell layer has two layers of woven polyester fibers (“scrim”) on the top and bottom. The scrim gives the plastic strength and prevents it from stretching excessively when molding. These unique properties make the material well suited for stacking multiple layers without having excessive bulking of material top lines. Both sides of the shell layer are coated with a layer of hot melt cement/glue/adhesive for easy attachment of various layers or other materials.

Abstract: An apparatus for supporting an arm during medical procedures such as radial catheterization and carpal tunnel procedures is disclosed. The apparatus includes an arm support section configured to support an arm of a patient, an intermediary valley section connected to a second end of the arm support section, a wrist flexing section connected to a second end of the intermediary valley section and configured to promote a downward flexing of the wrist, and a hand-hold section connected to the wrist flexing section. The hand-hold section is configured to hold the wrist in the downward flexing position.

Abstract: Methods of immobilizing the head of a patient include heating a thermoplastic mask preform to a formable temperature, forming the thermoplastic mask over at least a mouth of the patient, and pushing a mouth receiving end of a bite piece into a portion of the thermoplastic mask preform that is positioned over the mouth of the patient, which moves the portion of the thermoplastic mask preform into the mouth of the patient. The methods also include allowing the thermoplastic mask preform to cool from the formable temperature, causing the portion of the thermoplastic mask moved into the mouth of the patient to harden.

Abstract: Techniques and wearable appliances for monitoring bruxism, and/or for alleviating bruxism or sleep apnea related to bruxism are provided. In certain example embodiments, there is provided a custom teeth guard configured to be attached to at least some teeth in one of the upper or lower jaws, having at least two different non-zero amounts of padding arranged at positions located between teeth in the upper jaw and teeth in the lower jaw in accordance with predetermined strength of grinding of teeth at the positions. The custom teeth guard may be useful in helping to preempt apneic events and/or the like, e.g., by reducing the incidence and/or severity of teeth grinding.

Abstract: A bruxism guard is described. The bruxism guard includes a first U shaped tray having a top surface and a bottom surface, the top surface including a trough with a dental insert positioned therein, wherein the dental insert substantially conforms to a full arch of a subject's teeth, and a second U shaped tray having a top surface and a bottom surface, the top surface including a trough with a dental insert positioned therein, wherein the dental insert substantially conforms to a only a partial arch of the subject's teeth, wherein the bottom surfaces of the first and second trays oppose each other when positioned within the subject's mouth. Also described is a bruxism guard having a removable T-Bar that permits the bruxism guard to be interlocked in at least four different configurations.

Abstract: Facial Bands is an apparatus designed to relieve pressure and pain in the human face. This apparatus is made of two flexible bands, which includes various pouches with a material that can be heated or cooled to relieve pressure and pain on the human face; such as but not limited to the lower lip area, chin, cheeks, jawbone line, the sides of the face, and the temples. The two parts interlock and create one complete apparatus, with one band starting at the lower part of the chin and jawbone going upwards and latching at the top of the head, the other lower band piece goes from the lower lip around the jawline, going around the neck and latching at the back of the head.

Abstract: A thermal device having a waterproof pouch including a first member having a first perimeter and an first outer surface, and, a second member having a second perimeter and a waterproof second outer surface, wherein the first and second members are partially joined about the first and second perimeter, respectively, whereby a cavity is formed between the first and second members, an insert arranged to be removably disposed within the cavity, wherein the insert comprises thermal material capable of being heated or cooled, and, a barrier member having an inner surface, wherein the inner surface of the barrier member is releasably secured to the first outer surface of the first member via at least one attachment means.

Abstract: The application relates to a medical catheter for hypothermic treatment, with a catheter tube (10), which has at least one through-channel (11) and at least two temperature control channels (12, 13), and with at least one heat exchange element (14), in particular an expandable balloon, which is arranged in a distal catheter portion (15) of the catheter tube (10) and is fluidically connected to the temperature control channels (12, 13) in such a way that a temperature control circuit is formed. The application is characterized in that the catheter tube (10) has a smaller external diameter in the distal catheter portion (16) than in a proximal catheter portion (15).

Abstract: A vitrectomy apparatus is provided, including a pressure source, a cut valve connected to the pressure source, the cut valve configured to be turned on and off to provide pressure to selectively extend and retract a vitrectomy cutting device, a sensor configured to sense pressure provided from the cut valve, and a controller configured to control operation of the cut valve based on pressure sensed by the sensor. The controller is configured to monitor an amount of dwell time the vitrectomy cutting device remains open and monitor aspiration rate, and control a rate of material processed by the vitrectomy cutting device based on amount of dwell time and aspiration rate.

Abstract: Methods and systems for automatically pulsing different aspiration levels to an ocular probe are disclosed. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level, and applied to the probe in a pulsed manner.

Abstract: Methods and systems for automatically pulsing different aspiration levels to an ocular probe are disclosed. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level, and applied to the probe in a pulsed manner.

Abstract: Methods and systems for automatically pulsing different aspiration levels to an ocular probe are disclosed. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level, and applied to the probe in a pulsed manner.

Abstract: Methods and systems for automatically pulsing different aspiration levels to an ocular probe are disclosed. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level, and applied to the probe in a pulsed manner.

Abstract: Methods and systems for automatically pulsing different aspiration levels to an ocular probe are disclosed. The probe may be a phacoemulsification probe. A first aspiration level, supplied by a first pump, may be applied to the probe simultaneously with ultrasonic energy. A second aspiration level, supplied by a second pump, may be automatically switched from the first aspiration level, and applied to the probe in a pulsed manner.

Abstract: Transcorneal and fiberoptic laser delivery systems and methods for the treatment of eye diseases wherein energy is delivered by wavelengths transparent to the cornea to effect target tissues in the eye for the control of intraocular pressure in diseases such as glaucoma by delivery systems both external to and within ocular tissues. External delivery may be effected under gonioscopic control. Internal delivery may be controlled endoscopically or fiberoptically, both systems utilizing femtosecond laser energy to excise ocular tissue. The femtosecond light energy is delivered to the target tissues to be treated to effect precisely controlled photodisruption to enable portals for the outflow of aqueous fluid in the case of glaucoma in a manner which minimizes target tissue healing responses, inflammation and scarring.

Abstract: A method of cataract surgery in an eye of a patient includes identifying a feature selected from the group consisting of an axis, a meridian, and a structure of an eye by corneal topography and forming fiducial mark incisions with a laser beam along the axis, meridian or structure in the cornea outside the optical zone of the eye. A laser cataract surgery system a laser source, a topography measurement system, an integrated optical subsystem, and a processor in operable communication with the laser source, corneal topography subsystem and the integrated optical system. The processor includes a tangible non-volatile computer readable medium comprising instructions to determine one of an axis, meridian and structure of an eye of the patient based on the measurements received from topography measurement system, and direct the treatment beam so as to incise radial fiducial mark incisions.

Abstract: A method of cleaning and drying a hollow cavity with a cleaning apparatus which is made of a flexible, soft, and moisture absorbent material. A structural body of the cleaning apparatus contains a first wide base, a first narrow base, and a first conical lateral surface. The conical shape of the structural body allows the user to maintain a firm grasp during the cleaning and drying process. The cleaning process can be completed by either scarping an inner surface of the hollow cavity or by dabbing the inner surface of the hollow cavity. The flexible and soft material ensures that no damage is caused to the inner surface during the cleaning and drying process.

Abstract: Systems, methods, and apparatuses for forming a multi-function core for a dressing are described. The multi-function core includes a contact layer configured to be positioned adjacent to a tissue site, a wicking layer adjacent to the contact layer, an ion exchange layer adjacent to the wicking layer, an absorbing layer adjacent to the ion exchange layer, a blocking layer adjacent to the absorbing layer, and an odor-absorbing layer adjacent to the blocking layer. The contact layer, the wicking layer, the ion exchange layer, the absorbing layer, the blocking layer, and the odor-absorbing layer are coextensive and formed from a plurality of fibers disposed in a fibrous web. Methods of manufacturing the multi-function core are also described.

Abstract: A pressure bandage comprising an elastic band having a first end comprising a pocket member and a second end that is removably attachable to the first end. An inflatable bladder is placed in the pocket member and provides a substantially uniform pressure over a wound area when the band is placed on a patient and the bladder is inflated. The bladder is connected to a tube element which is used to inflate the bladder to the desired pressure. The elastic band may include a shoulder strap and may wrap over a patient's shoulder, across the patient's chest, and under the patient's opposite arm. The bottom side of the elastic band (facing the patient) may be made of a soft, absorptive material, and the bottom side of the pocket member may include an expandable mesh.

Abstract: Tapes and methods including an unbacked construction of at least one liquid layer adhesive that has been at least one of dried and cured. Occlusive tissue dressings, tapes and methods including an elastomeric drape and, for backed drapes and some unbacked drapes, a liquid component, at least partially cross-linked at least after one of drying and curing, suitable for application at a dressing-to-skin interface in order to create a substantially air-tight seal. The same or a different liquid component may be applied by a user at a tube-to-dressing interface of an elastomeric drape to create a similar air-tight seal around the tube, if not occlusively sealed during its manufacture. Featured are unbacked tapes, a drape with liquid sealant component, a liquid layered drape with liquid sealant component, and a liquid layered drape.

Abstract: A tampon for use in feminine hygiene. The tampon has an elongate body and a string. The elongate body has a first end, a second end, and an interior. The string has a first end, a second end, and an intermediate portion. The first end and the second end of the string are attached to the interior of the elongate body such that the first end and the second end are separated and the intermediate portion of the string forms a loop that extends from the second. end of the elongate body. The loop provides a grip to assist in removing the tampon.

Abstract: An incontinence detection device and system is disclosed.

Abstract: A system for managing female incontinence includes a body of biocompatible material configured to fit between the labia minora and the vestibule floor, the body having a surface configured to occlude the urethral meatus, an adhesive carried on at least a first portion of the surface and configured to provide a sealing engagement between the body and the urethral meatus, and wherein at least the adhesive includes a water gradient silicone hydrogel.

Abstract: A first fastening member joined to an absorbent article. A second fastening member joined to the absorbent article. The first fastening member and the second fastening member each include a first surface and a second surface opposite the first surface. The first surface of each of the first fastening member and the second fastening member includes a first engaging component and a second engaging component, respectively. The second surface of each of the first fastening member and the second fastening member includes a first receiving component and a second receiving component, respectively. The first engaging component is configured to engage a garment-facing surface of the second fastening member or a portion of a garment-facing surface of the absorbent article, and the second engaging component is configured to engage a garment-facing surface of the first fastening member or a portion of the garment-facing surface of the absorbent article.

Abstract: A disposable absorbent article includes a chassis and an absorbent core which is substantially cellulose free. The chassis may contain a topsheet and a backsheet. The absorbent core may be located between the topsheet and the backsheet and may include (i) a storage layer which comprises an absorbent particulate polymer material and has a wearer facing side and an opposed garment facing side, (ii) a first core wrap sheet covering the wearer facing side of the storage layer, and (iii) a second core wrap sheet covering the garment facing side of the storage layer, the first core wrap sheet being joined to the second core wrap sheet along at least one sealing zone.

Abstract: Embodiments of a fluid absorption and distribution enhancement (FADE) product comprises at least one flow media layer, and at least one superabsorbent polymer layer.

Abstract: A tampon disposal device includes a tubular stiffener, and a membrane conforming to the stiffener with an opening on one end and an enclosure opposite the opening. The membrane is folded inside the stiffener into a first layer attached to the stiffener; and second and third layers that form a lip surrounding the stiffener near a stiffener rim. The second layer folds over the rim, reversing direction to become the third layer lip portion. The third layer continues inside the stiffener. A weak adhesive attaches the lip to the outside stiffener. Another adhesive attaches the first layer to the second layer inside the stiffener. When a hand grasps a tampon string with the membrane and pulls on the string, the first adhesive allows the lip to separate and be pulled into the stiffener together with the tampon. Pushing inwardly on the stiffener seals the tampon inside the membrane.

Abstract: In one embodiment, an array of packages may comprise two or more different sizes of disposable absorbent articles. The Array Average Length Difference of at least the first and second absorbent articles in the array is less than about 65 mm and greater than about negative 10 mm. In another embodiment, a disposable absorbent article may have a Product Length is within about +/?40 mm of the Target Rise.

Abstract: Techniques and devices for securing a medical device to a patient-carrying device, such as a mechanical CPR device to a stretcher, are described herein. In one aspect, a medical device stabilization strap may include a first removable attachment shackle connected to a first end of a first strap. An adjustable quick release buckle may be disposed between a second end of the first strap and a proximal end of a second strap. A second removable attachment shackle may be connected to a distal end of the second strap. The first and second removable attachment shackles may each include a U-shaped bracket for removably engaging a medical device. The adjustable quick release buckle may adjust a length of the second strap, for example, to secure the medical device to the patient-carrying device.

Abstract: A shock absorbing support arm assembly for a litter support assembly that includes a support arm comprising a first end and a second end opposite the first end, a shock absorbing device disposed at the second end of the support arm, and a litter side shaft engagement mechanism disposed at the first end of the support arm. The support arm assembly may also comprise a mounting bracket connected at the second end of the support arm such that the shock absorbing device is positioned between the mounting bracket and the support arm. The support arm may move along an axis of the shock absorbing device and relative to the mounting bracket and may pivot about the axis relative to the mounting bracket.

Abstract: An apparatus for providing wheelchair access to a vehicle, including a deployable wheelchair access assembly coupled to the vehicle and deployable to a position in which one end of the assembly is in contact with the ground. The wheelchair access assembly can include multiple panels. Some embodiments include a control system for adjusting the angular relationship of one panel relative to another panel. Yet other embodiments include a sensor for measuring the inclination of the deployed assembly relative to earth's gravity. In yet other embodiments the vehicle includes a sensor for measuring the inclination of the vehicle relative to earth's gravity, and a plurality of suspension actuators for changing the inclination of the vehicle.

Abstract: A post-operative assistive sitting device configured to prevent pressure being applied to a post-operative patient's recovery area thereby allowing a patient to sit and conduct normal daily activities after a medical procedure. The post-operative assistive sitting device includes a chair that defines an opening and a series of cushions and paddings surrounding the opening to alleviate the pressure and discomfort from the recovery area without disturbing the buttocks as the patient sits or lies in a natural position.

Abstract: A chair assembly includes a pair of bases that are spaced apart. A primary arm is coupled between the pair of bases. A seat is coupled to the primary arm. The seat may support a user in a position that allows the user to stand with a minimal amount of effort. A rest arm is coupled to the primary arm. A backrest is coupled to the rest arm. The backrest may support the user in an upright position.

Abstract: Devices are disclosed herein which enable a user to rise from a seated position with minimal exertion.

Abstract: A seat support device is provided. The seat support is configured to receive a seat cushion and provide support to the cushion as well as providing two support handles above the cushion. The combination of these elements allows an elderly, disabled, or otherwise weakened person to easily rise from a seated to standing position.

Abstract: An adjustable bed having two bedframe halves and a gear hinge assembly for simultaneously translating the bedframe halves and for rotating one bedframe half. The gear hinge assembly is mounted to a carrier assembly that provides lateral movement and causes the bedframe halves to move from side to side. The gear hinge assembly includes an arm mounted to each bedframe half and a pair of nested cups, including gears, which are mounted to one of the arms. A pair of offset gear tracks interact with one of the gears at a time to cause the gear to rotate. When the gear rotates, the arm connected to the gear also rotates. The rotation of one arm and bedframe half occurs simultaneously with the translation of both bed halves.