Abstract: A method, system and device for addressing the reduction of snoring includes a removable or dissolvable strip of material that adhere to mucosal tissue of a person's soft palate to provide stiffening support therefore, thus reducing the occurrence of vibration of such tissue during sleep. Preferred embodiments include of a specially textured surface, either one both or at least the outer side of an adhesive strip (the side facing away from the mucosal tissue to which it is attached) that has anti-microbial characteristics, bioluminescent expressions, etc. and a surface topography that resists bioadhesion of undesired bacteria that are typically present in a human's mouth.

Abstract: Creation of surgical slush having desirable mechanical properties by chilling a closed slush container with liquid saline and an air gap. The closed slush container having interior surfaces that are smooth and hydrophobic to resist adherence of ice crystals. Moving the closed slush container so the contents move in a complex set of motions rather than constant rotation around a longitudinal centerline of the slush container as the liquid saline is converted into surgical slush with a mixture of liquid saline and ice crystals. Interior surfaces of the closed slush container move into and out of an air gap to help shed any ice crystals forming on the interior surfaces. In some instances, as the orientation of the closed slush container relative to gravity changes over time, different interior surfaces shed the ice crystals. An optional method for delivering surgical slush to the sterile field is included. The full range of the disclosure exceeds the scope of this brief abstract.

Abstract: The present application relates to systems and methods for altering temperature in a mammalian body. Optionally, the systems and methods can be used to lower or raise core body temperature of a mammalian subject. Optionally, the systems and methods can be used to lower or raise the temperature of glabrous skin of a mammalian subject.

Abstract: Described herein is a delivery device and methods for delivering an ocular implant into an eye. The delivery device includes a proximal handle portion; a distal delivery portion coupled to a distal end of the handle portion and configured to releasably hold an ocular implant and includes a sheath positioned axially over a guidewire; and a metering system configured to provide visual guidance regarding depth of advancement of an implant positioned on the guidewire into an anatomic region of the eye. Also disclosed is a device and method for loading an implant onto the delivery device.

Abstract: This disclosure relates generally to methods and devices for use in treating eye conditions with implantable drug delivery devices. One method includes introducing an implant into the suprachoroidal space, wherein the interior volume of the implant is plugged with a drug-release material comprising at least one active agent that elutes through at least one opening in the implant, wherein the drug-release material degrades from the interior volume of the implant over a period time.

Abstract: An eyedrop delivery system for the automated dispensing of eyedrop solution from bottles and ampoules. The system includes a battery and electronic control circuitry. A sprocket drive motor directs the advancement of a loop cartridge band containing eyedrop solution ampoules, moving each one at a time into position for dispensing. A motor rotates a cam to strike a push rod to compress each ampoule. The system includes an eyelid retracting leg assembly. The cartridge automatically advances the next full ampoule into position for dispensing and pushes the ampoule tip aside. The system helps assure that: (1) a known number of drops are dispensed; (2) the dispensed eyedrop(s) fall on the eyeball (by providing eyelid retracting legs to keep the eye open); and (3) the eyedrop(s) landing on the surface of the eye are confirmed using a drop dispensing sensor pair and a surface of the eye sensor pair.

Abstract: Devices that are adapted to insert corneal implants onto corneal tissue. Methods of using the devices include inserting the corneal implant into a pocket created in the cornea. Methods of use also include inserting the corneal implant onto corneal tissue after a flap has been created in the cornea. The devices can be adapted to deliver fluid to an implant holding space to at least assist in the deployment of the implant from the holding space and onto corneal tissue.

Abstract: A system for the removal of vitreous humor and other fluids from an eye and the reinjection of filtered vitreous humor into the eye is provided. The system comprises a hollow removal device, a filter, and an infusion device. The removal device includes an element configured to cut the vitreous humor and is configured to aspirate the vitreous humor from the eye. The filter is configured to create a filtered form of vitreous humor by separating the vitreous humor from undesired components in the vitreous humor. The infusion device is fluidly coupled to the filter and is configured to return the filtered form of vitreous humor into the eye.

Abstract: A surgical system comprises a hand piece, an irrigation conduit in fluid communication with the hand piece to carry fluid toward a surgical site, an aspiration conduit in fluid communication with the hand piece to carry fluid away from the surgical site, a pump interfacing with the aspiration conduit, the pump to create a vacuum pressure in the aspiration conduit to draw fluid through the aspiration conduit, a vacuum relief valve in fluid communication with the aspiration conduit to relieve the vacuum pressure in the aspiration conduit, a pressure sensor to detect a pressure associated with the surgical site, a controller in communication with the vacuum relief valve and the pressure sensor to control the vacuum relief valve to decrease the vacuum pressure in the aspiration conduit when the pressure detected by the pressure sensor is less than a first pressure threshold.

Abstract: A surgical hand piece comprises a shell, a channel having an irrigation conduit, and a sensor housing. The channel is coupled to the shell such that the proximal end of the channel is located at the proximal end of the shell and the distal end of the channel is located near the distal end of the shell. The sensor housing has an irrigation path extending through it. The sensor housing has a seal interface on one end. The seal interface end of the sensor housing is coupled to the proximal end of the channel such that the irrigation conduit of the channel is fluidly coupled to the irrigation path of the sensor housing.

Abstract: An implant for insertion through a punctum and into a canalicular lumen of a patient. The implant includes a matrix of material, a therapeutic agent dispersed in the matrix of material, a sheath disposed over a portion of the matrix of material and configured to inhibit the therapeutic agent from being released from the matrix of material into the canalicular lumen and to allow the therapeutic agent to be released from a surface of the matrix of material to a tear film, and a retention structure configured to retain the implant within the canalicular lumen.

Abstract: A steerable laser probe may include an actuation structure, a nosecone fixed to the actuation structure by one or more links and one or more link pins, a housing tube having a first housing tube portion with a first stiffness and a second housing tube portion with a second stiffness, and an optic fiber disposed in the housing tube and the actuation structure. A compression of the actuation structure may be configured to gradually curve the housing tube and the optic fiber. A decompression of the actuation structure may be configured to gradually straighten the housing tube and the optic fiber.

Abstract: A device operative having a rotating cleaning tip for cleaning a narrow channel, such as an ear canal. In one embodiment, the tip is coupled to a handle with a motor that rotates the tip. The rotating tip has a plurality of strips that bow outwardly, scraping debris from the walls without debris accumulating and impacting along a channel wall. The bowing strips provide entry slits to capture debris into the tip, the strips closing after capture, removing debris when the tip withdraws from the channel. The device has a safety ring disposed around the tip, the safety ring operative for limiting penetration into a narrow canal when cleaning.

Abstract: Hearing protection devices, e.g., push-to-fit earplugs, having a tip cavity in the sound attenuating body and methods of manufacturing the hearing protection devices are described herein.

Abstract: A modular, reduced-pressure, wound-closure system for providing a closing force on a surface would includes a flexible strap operable to be formed into a closed loop inbound and around the surface wound and a plurality of modular closing members coupled to the flexible strap. A reduced-pressure source is fluidly coupled to the plurality of modular closing members. The modular closing members are operable to generate a closing force on the surface wound. A portion of the modular closing members are releasably attached to the patient's epidermis proximate the surface wound and another portion are attached to the flexible strap. A reduced pressure from the reduced-pressure source is delivered to each modular closing member to generate the closing force on the surface wound. Methods and other systems are presented.

Abstract: The present invention relates to a method for fabricating absorbent article having multiple layers, and deformed zones of targeted performance, and colored regions, the method comprising the steps of forming discrete features on at least one layer, printing colored regions on at least one layer, integrating multiple layers to form an absorbent assembly, and cutting the absorbent assembly into individual absorbent articles, wherein the steps are carried out continuously.

Abstract: The present invention generally relates to sanitary absorbent articles and in particular to disposable feminine sanitary absorbent articles that are extremely thin, highly absorbent and have superior structural integrity properties.

Abstract: A pant-like garment having an elastomeric film laminate front panel and back panel. A front leg elastic member disposed adjacent the front panel leg edge. A back leg elastic member disposed adjacent the back panel leg edge. The absorbent garment having a leg elastic covering panel which extends between and interconnects the front panel to the back panel such that the front leg elastic member is sandwiched between the leg elastic covering panel and the front panel and such that the back leg elastic member is sandwiched between the leg elastic covering panel and the back panel. The length of the leg elastic covering panel is less than the garment length. An absorbent composite is attached to the leg elastic covering panel and a pair of side seams connects the front region to the back region to define a waist opening and a pair of leg openings.

Abstract: A dental isolator in the form of a U-shaped absorbent member having a first portion and a second portion disposed on either side of a third central portion and a retainment member, which retainment member transversely engages both the first portion and the second portion of the absorbent member, the retainment member being adapted to fit between adjacent teeth of a dental patient, the first portion of the U-shaped absorbent member being adapted to be disposed on the internal side of the teeth of a dental patient between the teeth and the tongue of the patient, the second portion of the U-shaped absorbent member to be disposed between the cheek and the mucobuccal fold of the patient with the central portion of the U-shaped absorbent member surrounding a rear tooth of the patient, the distal end of the second portion of the U-shaped absorbent member being tapered.

Abstract: An early warning method and a device for preventing a wheelchair from tipping over are described. The early warning method includes projecting a laser light pattern, scanning the laser light pattern, making a comparison to determine whether the ground is a barrier terrain, and issuing an early warning to the user in situations of risk. The laser light pattern is projected onto the ground and compared with a standard pattern. The early warning is generated and is one selected from a group consisting of a beep, a warning message and a vibration to alert the wheelchair user to the danger of the barrier terrain.

Abstract: A rolling footrest is provided and a method of using such by a wheelchair occupant. The footrest may optionally include a foot retainer, a platform and freely rolling castors. In some embodiments, replacing a fixed footrest will shorten the length of the wheelchair enabling the wheelchair to traverse sharp curves. In some embodiments, the footrest may include a swivel lock and/or a ratchet. In some embodiments the footrest may be used for therapeutic exercise. In some embodiments, the footrest may be used for propelling a wheelchair.

Abstract: A surgical table including a patient support structure and a base assembly including a first and a second support column supporting respective ends of the patient support structure. The patient support structure including a head end section and a foot end section, the head end section coupled at a pair of outer ends to the first support column, the foot end section coupled at a pair of outer ends to the second support column, the head and foot end sections each comprising a pair of inner ends that are pivotally and slidingly coupled together at an inward articulation, each of the inner ends of the head end section comprise a slot at the inward articulation, each of the inner ends of the foot end section are coupled with the respective slot via a hinge pin that engages the slot, the hinge pin configured to pivot and slide within the slot.

Abstract: A central bed having a longitudinal bed frame and a bed section mounted to the frame for rotation about a substantially vertical axis between a home position aligned with the bed frame and an away position.

Abstract: A surgical positioning system includes a flexible air-impermeable shell filled with beads that is wrapped against the patient and subjected to a vacuum to hold the patient in place. An air-impermeable top wall can be joined with an air-impermeable bottom wall to define a plurality of chambers. Each of the chambers can include a peripheral edge that extends around the periphery of the respective chamber. The plurality of chambers can include a first shoulder chamber, a second shoulder chamber, and a main chamber.

Abstract: According to one embodiment, a rehabilitative training device for use with a stroke patient includes a first component that is operatively coupled to a first body part (unaffected body part) of the patient and a second component that is operatively coupled to a second body part (affected body part) of the patient. The first component and second component are operatively coupled to one another such that motion of the first component as a result of movement of the first body part by the user causes the second component and second body part to move in a symmetrical motion.

Abstract: The sequential compression device for treatment and prophylaxis of deep vein thromboses includes a compression sock having a plurality of electromechanical units positioned along the calf muscle of a user's leg. Each of the electromechanical units includes a front housing component and a back housing component. The front housing component of the unit includes a compressor piston positioned in communicating relation with the user's calf muscle and the back housing component of the unit includes a magnet and a copper coil. The magnet is positioned in communicating relation with the compressor piston of the front housing component. Upon activation, the compressor piston selectively compresses the small saphenous vein to simulate the effect of the calf muscle during walking and promote the flow of blood back to the user's heart.

Abstract: A lip enhancement and enlargement device includes a suction element and a lip shaper coupled to the suction element. A lip shaper may include one or more features that allow the device to shape and contour lips. A lip shaper may include one or more contouring elements that change the shape of an upper lip, for example. A lip shaper may also include shaping and contouring elements that form a fuller, unitary lip lobe or two fuller, lip lobes. Lip enhancement and enlargement kits and methods are also disclosed.

Abstract: A wearable thorax percussion device for dislodging mucous buildup in the airways of a human patient, the device comprising frame elements and electromechanical actuators retained by the frame elements to intermittently percuss the thorax, and an electronic controller and power source for generating and modulating an electrical signal to energize the actuator. The frame elements may be interconnected by a garment, or fasteners and elastic or adjustable strapping.

Abstract: A system that applies vibration to a desired region of a human body including a plurality of vibratory stimulators installed in a flexible material; a programmable control unit (PCU) connected to each said vibratory stimulator a plurality of sensors to collect biofeedback data; a set of programs for the operation of the PCU; a biomechanical database stored in a computer and being populated by the biomechanical data collected by the sensors after application of each said predefined pattern of vibration; and an algorithm to analyze and rank said patterns of vibration according to a ranking factor, wherein a user can choose a pattern of vibration that has a higher ranking factor.

Abstract: A lighted jet assembly for through hole mounting to a panel in a bathing installation. In an exemplary embodiment, the assembly includes a jet body configured for mounting in a hole formed in the bathing installation panel. A light receptacle is formed with the jet body, the light receptacle configured to receive a light source element. A jet barrel assembly includes a hollow barrel structure configured for insertion into the jet body channel through the open second end of the jet body. A blind structure includes a hollow cylindrical portion having at a first end a flange portion extending over a limited angular extent, and a second end configured to be secured within the open interior region of the jet barrel structure. The blind structure is fabricated of an opaque material, and configured for rotation with the jet barrel assembly relative to the jet body.

Abstract: Certain embodiments are directed to methods of treating a metabolic disease in a subject using a fully implantable electrical stimulation system to provide or administer a therapy. In certain aspects a stimulation lead is implanted proximally to a stomach acupoint, the stimulation lead being coupled to an implantable signal generator; and stimulating the acupoints using the signal generator to treat the metabolic disease.

Abstract: An adaptor for coupling with a medical container, including: a tubular body receiving a pierceable elastomeric piece, defining an inner cavity of the adaptor, the pierceable elastomeric piece being movable within the tubular body between a first position, in which a distal part of the pierceable elastomeric piece forms a seal of the cavity, and a second position, proximally spaced from the first position, in which the distal part opens the seal of the cavity, an air inlet, a filtering system for filling the inner cavity with decontaminated air, and a gripping member for securing the adaptor to the medical container. Also, an assembly comprising such an adaptor and a medical container.

Abstract: Device and method for needle penetrating and filling a chamber with a predetermined substance, and hermetically resealing a resulting needle hole in the device by applying radiation thereto. The needle penetrable and resealable portion defines a predetermined wall thickness in an axial direction thereof, and may include a thermoplastic that substantially prevents the formation of particles released into the chamber from the needle penetrable and resealable portion during penetration by and withdrawal of the needle. Such thermoplastic may include a predetermined amount of pigment that allows the thermoplastic to substantially absorb laser radiation at a predetermined wavelength, substantially prevent the passage of radiation through the predetermined wall thickness thereof, and hermetically seal a needle aperture formed in the needle penetration region thereof in a predetermined time period.

Abstract: A drug mixing system including at least one receptacle port adaptor adapted to be inserted into a port of a fluid receptacle, at least one syringe adaptor adapted to be attached to a syringe and to the at least one receptacle port adaptor and at least one vial adaptor adapted for connection to a vial containing a drug and adapted for connection to the at least one syringe adaptor, the system being characterized in that at least one of the receptacle port adaptor, the at least one syringe adaptor and the at least one vial adaptor being vented to the atmosphere in a manner which prevents release to the atmosphere of possibly harmful contents of the vial in a liquid, solid or gaseous form.

Abstract: The present invention relates to a device for introducing filling material (21) into capsules (22), comprising a filling device (25) for feeding filling material (21) to the capsules (22), a capsule holder (30) with at least one row of seats (31) in which the capsules (22) that are to be filled are arranged, a station arrangement with several stations arranged one after another, wherein the station arrangement comprises at least one filling station (5) and a synchronously operating drive, and a movement device which, at the capsule-filling station (5), executes a relative movement between the filling device (25) and the capsule holder (30), wherein the filling device (25) adopts, relative to the capsule holder (30), at least a first filling position for filling a first capsule and a second filling position for filling a second capsule.

Abstract: The subject matter of this specification describes, among other things, devices and processes for providing measured doses of oral medication to patients, such as infants or other vulnerable patients.

Abstract: A set of a first and a second preparation are intended to be mixed before or during an endodontic treatment to form an endodontic irrigation solution. The first preparation includes an oxidizing agent. The second preparation includes antibacterial nanoparticles treated to slow their oxidation by the oxidizing agent. The antibacterial nanoparticles are, for example, encapsulated in shells in a hybrid core-shell structure. In one variation, the antibacterial nanoparticles are made from an alloy of at least two elements, one of the elements being more resistant to oxidation than the other.

Abstract: A powder-liquid dental curable material kit composed of (A) a liquid material and (B) a powder material, wherein the liquid material (A) contains (a1) a radically polymerizable (meth)acrylic monomer, (a2) an organic halogen compound and (a3) a radical chain transfer agent; the powder material (B) contains (b1) non-crosslinked resin particles, (b2) a pyrimidinetrione compound and (b3) an organic metal compound; and (Z) a peroxide is blended in at least one of the liquid material (A) and the powder material (B). This curable material kit is capable of reducing the heat generation during the curing of a curable material which is a mixture of the liquid material (A) and the powder material (B) and is not susceptible to the excessive prolongation of the curing time even when the curable material is cured by a brush-on technique, thereby ensuring an appropriate curing time for both of a brush-on technique and a kneading technique.

Abstract: Dental cement compositions (including two-part compositions), kits, and related methods are used for bonding a dental prosthetic appliance to a tooth. A first part includes an amine activator component and a zinc oxide reactive filler, while a second part includes a polymerization initiator (e.g., benzoyl peroxide) and a polymerizable component having a structure including at least one acrylate or methacrylate group at one end and a carboxylic acid group at another end. A temporary cement composition advantageously exhibits reduced compressive and/or bonding strength relative to permanent cement compositions, which provides sufficient strength to facilitate normal use of the teeth while the provisional appliance is in use, while also facilitating easy removal of the provisional appliance for replacement with a permanent appliance at a later time.

Abstract: The invention is related to a dental impression composition which is curable at a temperature below about 50 C, the composition comprising: (A) a curable organopolysiloxane polymer as component (A), (B) a crosslinker compound capable of cross-linking said organopolysiloxane polymer as component (B), (C) a catalyst as component (C) capable of catalyzing a crosslinking reaction of component (A) and component (B), (D) a hydrophilizing agent as component (D), (E) a filler as component (E), (F1) a stabilizer as component (F1) selected from compounds comprising a phosphite moiety and mixtures thereof, (F2) a stabilizer as component (F2) selected from antioxidants and mixtures thereof, the composition being present in the form of a base paste and a catalyst paste physically separated from another, the base paste comprising components (A), (B), (D), (E), (F1), (F2), the catalyst paste comprising components (A), (C), (E).

Abstract: Inventive embodiments disclosed herein relate to gel volume mascara. The mascara includes water in a concentration of at least about 45% by weight; disodium ethylenediaminetetraacetate; Polysorbate 20; Black iron oxide; One or more waxes selected from the group consisting of beeswax, Cera Carnauba/Copernicia Cerifera (Carnauba) Wax/CIRE de Carnauba, and paraffin in a concentration of 15-20% by weight; and a synthetic layered silicate, insoluble in water, in a concentration effective for forming a colloidal dispersion with the water.

Abstract: Cosmetic antiperspirants for nonaerosol use, having a content of methanesulfonic acid and/or at least one physiologically acceptable salt of methanesulfonic acid, which exhibit less textile staining than known antiperspirants.

Abstract: Novel retinoic acid derivatives and a process for their preparation are described.

Abstract: A scalp care composition directed to a scalp care composition comprising from about 0.05% to about 5% of an anti-dandruff active, from about 0.1% to about 25% of one or more organic solvents, from about 1% to about 99% of a volatile carrier wherein the anti-dandruff active is soluble in the scalp care composition.

Abstract: Personal care formulations containing alkyl ketal esters having the structure wherein a is 0 or an integer of 1 to 12; b is 0 or 1; R2 is a divalent C1-8 group optionally substituted with up to 5 hydroxyl groups; and R1 is C1-6 alkyl.

Abstract: Oral compositions containing a polyorganosilsesquioxane particle, preferably polymethylsilsesquioxane particles, a fluoride ion source, and an orally-acceptable carrier. Method of using such compositions for the cleaning and polishing of dental enamel, such methods including the step of applying such oral care compositions to the teeth of a user.

Abstract: The compositions and methods of this invention relate to a rinse-off skin care composition containing hydrophobic, linear cellulose particles having an average length of from about 1 to about 1000 ?m, a particle aspect ratio from about 1000 to about 2 and a thickness of from about 1 to about 500 ?m; at least one cleansing agent selected from the group consisting of a saponified fat and a surfactant; and a cosmetically acceptable carrier.

Abstract: The compositions and methods of this invention relate to a rinse-off skin care composition containing hydrophobic, linear cellulose particles having an average length of from about 1 to about 1000 ?m, a particle aspect ratio from about 1000 to about 2 and a thickness of from about 1 to about 500 ?m; at least one cleansing agent selected from the group consisting of a saponified fat and a surfactant; and a cosmetically acceptable carrier.

Abstract: A skin care composition having from about 0.01% to about 5%, by weight, of an superabsorbent polymer which is a sodium polyacrylate, sodium polacrylate starch, sodium acrylates crosspolymer-2 or mixtures of these and a portion of the polymer comprises a grafted starch material. The superabsorbent polymer is particulate where the particles have an average particle size in the range of from about 5?-30?, and the individual particles in their dry or un-swollen condition are substantially non-spherical, flat, platelet, or elongated in shape. The particles have an absorption capacity of at least about 1000 times their initial dry or un-swollen volume. Additionally, the skin care composition contains from about 0.01-10% of a dry powder that is either starch or silicone based and wherein the dry powder is coated with a silicone based material. Further there is provided a UV active.

Abstract: The present invention relates to a cosmetic make-up or care composition including an oily phase comprising at least one liquid polyester obtained by condensation of unsaturated fatty acid dimer and/or trimer and diol, said composition being free from lipophilic gelling agent or comprising at the most 10 wt. % thereof, relative to the weight of the composition. The present invention also relates to a method of make-up of the face and body with the the composition.