Abstract: The invention relates to an instrument which has been developed to be used in macular hole surgeries closes and repairs the macular hole by drawing the retina, wherein it comprises a holder comprising at least one shaft connected to the handle, and at least one pressure leg positioned to the end of the shaft.

Abstract: A surgical system provides hands-free control of at least one surgical tool includes a robot having a tool connector, a smart tool attached to the tool connector of the robot, and a feedback control system configured to communicate with the smart tool to provide feedback control of the robot. The smart tool includes a tool that has a tool shaft having a distal end and a proximal end, a strain sensor arranged at a first position along the tool shaft, at least one of a second strain sensor or a torque-force sensor arranged at a second position along the tool shaft, the second position being more towards the proximal end of the tool shaft than the first position, and a signal processor configured to communicate with the strain sensor and the at least one of the second strain sensor or the torque-force sensor to receive detection signals therefrom.

Abstract: The present invention is an intraocular surgery system using a Venturi pump and capable of preventing clogging due to nucleus fragments, despite a reduced aspiration flow rate.

Abstract: A phacoemulsification needle (100, 100A, 100B, 1000, 100D, 200, 200A) is provided for emulsifying body tissue. The needle (100, 100A, 100B, 1000, 100D, 200, 200A) is adapted to be attached to a phacoemulsification handpiece that imparts a vibration to the needle (100, 100A, 100B, 100C, 100D, 200, 200A). The needle (100, 100A, 100B, 1000, 100D, 200, 200A) has a body (104, 220, 220A) with a distal end (99), a proximal end (106), and an aspiration passage (124) extending between the proximal and distal ends (99, 106). The aspiration passage (124) defines a longitudinally-extending central body axis (110, 110A, 110B, 1100, 110D). The aspiration passage (124) is enlarged at the distal end (99) to define a tip (102, 102A, 102B, 1020, 102D, 210, 210A).

Abstract: Various arrangements of fluidics systems are disclosed. In one arrangement, an aspiration circuit for a fluidics system is disclosed that selectively controls aspiration. The aspiration circuit comprises an aspiration line operatively connected to a surgical instrument, an aspiration exhaust line operatively connected to a waste receptacle; an aspiration vent line connected at a first end to the aspiration line; and a selectively variable vent valve operatively connected to the aspiration vent line. The variable vent valve may be selectively moved to vary aspiration pressure within the aspiration line. Other fluidics systems are disclosed that include a selectively positionable irrigation valve that may also be incorporated into a fluidics system that includes a variable vent valve.

Abstract: A Device for producing cuts or perforations on a human or animal eye at the anterior or posterior opening of the eye lens (capsulatomy, rhexis) with a cutting element that can be inserted into the interior of the eye and a drive device which is arranged outside of the eye in order to cause movement, in particular oscillatory vibrations or rotation of the cutting element inside the interior of the eye, the drive device having a field generator for generating a magnetic or electromagnetic excitation field and the cutting element can be excited, in particular driven, by way of the excitation field generated by the field generator.

Abstract: A pressure-driven valve is disclosed. The valve includes a housing, a fluid flow channel, and a deflectable portion. The housing comprises a fluid inlet and a fluid outlet. The fluid flow channel extends between the fluid inlet and the fluid outlet. The deflectable portion is disposed within the housing, and defines a portion of the fluid flow channel. The deflectable portion is configured to deflect to increase and decrease a size of the fluid flow channel to regulate fluid flow from the fluid inlet to the fluid outlet. The deflectable portion is disposed and arranged to deflect as a result of pressure differentials between a reference pressure, a fluid flow channel pressure, and an outlet pressure representative of fluid pressure at the fluid outlet.

Abstract: A method and delivery system are disclosed for creating an aqueous flow pathway in the trabecular meshwork, juxtacanalicular trabecular meshwork and Schlemm's canal of an eye for reducing elevated intraocular pressure. Pulsed laser radiation is delivered from the distal end of a fiber-optic probe sufficient to cause photoablation of selected portions of the trabecular meshwork, the juxtacanalicular trabecular meshwork and an inner wall of Schlemm's canal in the target site. The fiber-optic probe may be advanced so as to create an aperture in the inner wall of Schlemm's canal in which fluid from the anterior chamber of the eye flows. The method and delivery system may further be used on any tissue types in the body.

Abstract: A steerable laser probe may include a handle, an actuation structure, an optic fiber, and a housing tube. The housing tube may include a first housing tube portion having a first stiffness and a second housing tube portion having a second stiffness. The second stiffness may be greater than the first stiffness. The optic fiber may be disposed within the housing tube and within an inner bore of the handle. A compression of the actuation structure may be configured to gradually curve the optic fiber. A decompression of the actuation structure may be configured to gradually straighten the optic fiber.

Abstract: The present invention discloses an auto darkening mask which comprises a weld cap and a filter mechanism, wherein the filter mechanism includes a lens module, a connecting line and a regulating system; and the weld cap is provided with a visible window. The lens module is assembled inside the weld cap and is opposite to the visible window of the weld cap. The regulating system is located at the outside of the weld cap and connected with the weld cap, and the lens module is connected with and controlled by the regulating system through the connecting line. The auto darkening mask is very convenient to regulate and saves labor.

Abstract: A tinnitus treatment system comprising a sound processing unit, a haptic stimulus unit and an audio delivery unit. The sound processing unit comprises a processor input for receiving an audio signal; and a digital signal processor operable to analyse said audio signal and generate a plurality of actuation signals therefrom which are representative of said audio signal. The digital signal processor is further operable to spectrally modify said audio signal in accordance with a predetermined modification profile to generate a modified audio signal. The haptic stimulus unit comprises an array of stimulators each of which can be independently actuated to apply a tactile stimulus to a subject; and a stimulus unit input for receiving the plurality of actuation signals generated by said digital signal processor and directing individual actuation signals to individual stimulators.

Abstract: An expansible ear canal insert for treating TMJ disorders and headaches which acts directly on the TMJ and associated ligament and muscle structures to reduce stress and loads placed on the articulator disc located between the temporal bone and the mandible, as well as supportive muscles and ligaments near the TMJ. The insert is adapted to expand by application of body heat. In the expanded condition, the insert provides support to the TMJ and associated ligament and muscle structures.

Abstract: A thermal reflective layer provided either separately or in combination with a wound dressing is provided. The wound dressing typically includes a top layer, and a bottom layer on an opposite side of the wound dressing from the top layer. The thermal reflective layer is positioned between the top and bottom layers and is formed of a plurality of thermal reflecting domes arranged in an array configuration with apexes of each dome oriented toward the bottom layer of the wound dressing facing the wound upon which the wound dressing is configured for placement. This configuration reflects body heat back on to the wound when the wound dressing is in place, and more rapidly increases the wound surface to a physiologically optimum healing temperature more rapidly than other conventional wound dressings, which improves the facilitation of wound healing. The configuration also enables wound visualization, and required wound piercing procedures.

Abstract: An article of manufacture for a bony prominence under casts, splints and or other devices utilized to hold the limb in a fixed position for an extended period of time. The article consists of a pressure relieving pad from a base substrate with a predetermined design formed from a gel material with an adhesive quality. In another embodiment, the article consists of a pressure relieving pad formed from a gel material base substrate combined with a fibrous substrate with a predetermined design of the pressure relieving pad. Each article includes at least one ventilation channel cut through the base substrate and/or fibrous substrate, e.g. the ventilation channel may have a single or multiple cut incision. The ventilation channel functioning to increase the padding around the base of the prominence thereby providing extended comfort and fitting of a rigid splint, cast or other fixing device.

Abstract: A method of evaluating the smoothness of a topsheet or a backsheet of a disposable absorbent article is disclosed, the method comprising: (a) providing an element having a surface; (b) providing a first disposable absorbent article having a topsheet, a backsheet, and an absorbent core located between the topsheet and the backsheet; (c) rubbing the surface of the element against the topsheet or the backsheet of the disposable absorbent article along a predetermined length of the disposable absorbent article with a predetermined force; and (d) inspecting the surface of the element after it has been rubbed to evaluate if the surface of the element or the topsheet or the backsheet of the disposable absorbent article is damaged or destroyed by the rubbing against the topsheet or the backsheet of the disposable absorbent article.

Abstract: Pull-on disposable absorbent articles comprising an elastomeric belt, a central chassis, and graphics.

Abstract: A textured laminate structure and absorbent articles having a component formed of the textured laminate structure are disclosed. The textured laminate structure may have a first layer formed of a nonwoven web having a preexisting pattern of first apertures therethrough, a second layer, and one or more elastic members disposed between the first and second layers in a prestrained condition. The laminate structure may be discontinuously joined or bonded such that the first layer is joined or bonded to the structure in first portions and unjoined or unbonded to the structure in second portions. The structure provides a stretch laminate with tactilely and visually interesting features, and may be used to form components of a disposable absorbent article such as a side panel thereof.

Abstract: An undergarment includes at least one panel of stretchable loop material. The panel of stretchable loop material is connected to a main body of the undergarment such that it can stretch around one side of wearer's waist or hip. The stretchable loop material is configured such that it can releasably connect to a plurality of engaging elements. The engaging elements can be hooks of a hook and loop fastening system. The undergarment is configured such that it can be easily concealed beneath clothing and can be easily positioned and removed by a wearer. A method of disposing an undergarment includes rolling or folding the main body of the undergarment and tying panels of stretchable loop material around the rolled or folded portion to encase the rolled or folded portion between the panels of stretchable loop material.

Abstract: A disposable absorbent article may include a topsheet, a backsheet, an absorbent core disposed between the topsheet and the backsheet, and a leg gasketing system. The leg gasketing system may include an inner cuff and an outer cuff; the inner cuff may include an inner cuff folded edge and an inner cuff material edge and the outer cuff may include an outer cuff folded edge and an outer cuff material edge such that the web of material is folded laterally inward to form the outer cuff folded edge and folded laterally outward to form the inner cuff folded edge.

Abstract: A male urine receptacle is provided that includes a liquid permeable inner layer, a liquid impermeable outer layer and an absorbent core located therebetween. The inner layer, outer layer and absorbent core are assembled together to form a layered assembly, which, when folded into a into a “U” configuration, defines a front portion and a back portion of the receptacle. At least a portion of the side edges between the front portion and the back portion are closed by sealing or otherwise securing together the side edges of the layered assembly. At least one of the closed sides forms an expandable gusset and, preferably, both sides include at least one gusset. A closure mechanism is configured to adjust the open, upper periphery of the receptacle to provide a comfortable fit onto a penis, thus retaining the male urine receptacle on the penis.

Abstract: According to one embodiment, a roll-in cot may include a support frame, a pair of back legs, a pair of front legs, and a cot actuation system. The pair of back legs and the pair of front legs can be slidingly coupled to the support frame. Each of the pair of front legs can include a front wheel and an intermediate load wheel. The intermediate load wheel is offset from the front wheel by a load wheel distance. A front actuator can raise the pair of front legs such that the front wheel and the intermediate load wheel of each of the pair of front legs are aligned along a loading level. The intermediate load wheel of each of the pair of front legs can be offset from the pair of back legs by a loading span. The load wheel distance can be greater than the loading span.

Abstract: A bed device includes: an operation section that receives an operation input; a controller that controls a movement of the bed in accordance with the operation input; a detector that detects a position of a patient on the bed; and, a limitation table that stores a limitation area set on the bed in association with a limitation content, wherein when the position of the patient detected by the detector is included in the limitation area, the limitation content is read out from the limitation table so as to control the controller in accordance with the limitation content. With this configuration, it is possible to provide a higher safety bed device which can not only notify the danger based on the bed movement but also limit the movement of the bed in accordance with the status of the patient or the bed device.

Abstract: The present invention includes an apparatus, to be used during a medical procedure to support a patient's arm, which generally includes an armboard and an optional wrist support device attached to a patient that may be removably connected to the armboard, and a general method of use.

Abstract: A method and apparatus for improving adenoma detection, including applying compression to the abdomen of a patient and maintaining compression of the abdomen of the patient during withdrawal of an endoscope. The compression may be applied by wrapping a band of elastic material around the abdomen of a patient and connecting one end of the band to another portion of the band to maintain tension in the band in order to apply compression to the abdomen of the patient. Aspects may also include tensioning the band prior to connecting the one end of the band to the another portion of the band to apply a desired degree of pressure to the patient's abdomen through contraction of the band across at least a portion of the patient's abdomen.

Abstract: A walking assistance device configured to permit the independent movement of an individual via simulated weight reduction is described. The device is configured to partially suspend a portion of a user's weight via a seat-lifting system, facilitating the movement of a user with experiencing difficulty walking without assistance. The system of the device preferably employs a seat, a hydraulic or electric seat-lift mechanism, a seat restraint, a frame, wheels, a brake system, and a power source. The seat-lift mechanism is configured to rise and lower the seat, enabling the user to control the percentage of weight lifted, while the feet of the user remain in partial contact with the floor. The frame forms the structure and support of the device, and is configured to move laterally via wheels on the bottom of the frame of the device.

Abstract: An apparatus and method for self-regulating therapeutic pressure massage are disclosed. An example embodiment includes an apparatus comprising: a handle; a force self-regulating mechanism captured with the handle; a rod in contact with the force self-regulating mechanism at a first end of the rod, the rod compressing the force self-regulating mechanism when force is applied to the handle; and a tip attached to a second end of the rod.

Abstract: A back scratcher which includes (a) a scratcher head containing a plurality of scratching teeth on its underside, projecting outward at a right angle to the plane of the scratcher head and being a consistent length to provide an even scratching surface; (b) an elongated shaft with a first end connected to the back of the scratcher head opposite the scratching teeth and a second end connected to (c) a handle which forms a loop to provide a means for gripping and hanging for storage.

Abstract: Disclosed herein are embodiments of a massage roller, and methods of making and using such a massage roller, whereby the massage roller includes a massage roller body comprising a generally circular cross section, opposing first and second end portions, a convex medial portion, a first concave lateral portion axially extending between the first end portion and the convex medial portion, and a second concave lateral portion axially extending between the second end portion and the convex medial portion; wherein said massage roller body is asymmetric about a massage roller body vertical centerline.

Abstract: A vibration ring includes a vibration module and a latex ring. The vibration module is provided with at least a battery, a circuit board and a vibration motor that are connected electrically in a spherical shell, along with a switch that is exposed out of the shell. The latex ring includes an annular wearing part that is processed with latex, and a spherical vibration part that encloses the shell of the vibration module. The spherical vibration part and the enclosed vibration module act onto a female's clitoris without pressing on other parts of the body, so as to increase the comfortableness in wearing the vibration ring and form a better exciting effect in vibration.

Abstract: A clitoris vibrator. It comprises a handle (4) that incorporates a motor (7) and a control button (3) that activates the motor (7) and at least one vibrating ball that is powered by the motor (7); comprising two flexible arms (1) that incorporate a vibrating ball (6) therein; and a connection point (5) of the two flexible arms (1) that incorporates a vibrating ball (6) from where the handle (4) extends. The flexible arms (1) form a V shape that imitates the structure of the inner clitoris thus meaning that, by placing the connection point (5) on the clitoral glans, the arms (1) adapt to the contours where the internal organs of the clitoris are located. Said arms (1) further comprise a narrow portion in the shape of an elbow (2), manufactured with flexible material; and a wider portion where the vibrating ball (6) is located. The portion of the arms (1) that comes into contact with the body has a rounded contour which enables the vibration pulse to be intensified.

Abstract: An insertion apparatus for use in a vaginal or rectal cavity or a vaginal or rectal opening of the human body. The insertion apparatus has a base body, which in turn has a working body. In addition, a pulling device used for removing the working body from the cavity or the opening is firmly mounted on the base body. The pulling device is formed by a finger grip that is elastically formed, at least in part. The finger grip is elastically deformable between a neutral position and a removal position, and the finger grip is made, at least in part, of an elastic material. The insertion apparatus may in particular be configured as a massage apparatus or as a tampon.

Abstract: Aspects herein relate to a stimulation device. The stimulation device includes a flexible board configured for personal use, an array of one or more stimulating components disposed throughout at least a portion of the flexible board, and a stimulation controller in communication with at least one of the one or more stimulating components, the stimulation controller configured to process a stimulation signal that engages or disengages at least one of the one or more stimulating components.

Abstract: A shaking device includes at least one pad, a mover configured to reciprocally move the pad, and a mount configured to support the mover. The shaking device may be connected with a medical device using a feedback system. The shaking device may be configured to change settings based on readings from the feedback system.

Abstract: A chest compression monitor for measuring the depth of chest compressions achieved during CPR. A displacement detector produces a displacement signal indicative of the displacement of the CPR recipient's chest toward the recipient's spine. A signaling mechanism provides chest compression indication signals prompting a CPR provider to provide a chest compression force at a desired depth and rate. The device is held to the dorsal surface of the hand during use and provides a display for feedback, which is readily visible to the CPR provider.

Abstract: Methods and devices for chest compression depth measurement for CPR.

Abstract: An acupressure device and methods for application of the acupressure device to appendages of the human body for therapy and/or the treatment of various ailments.

Abstract: This disclosure discloses a pair of foot massage physiotherapy plates. The foot massage physiotherapy plates comprise bottom plates, foot reflex zone massage blocks and foot acupuncture point massage posts; the foot reflex zone massage blocks are connected with the bottom plates through massage block bolts and the foot acupuncture point massage posts are connected with the foot reflex zone massage blocks through massage post bolts; massage bulges are arranged on the front surfaces of the foot reflex zone massage blocks. The foot massage physiotherapy plates disclosed by the disclosure change the design of fixed massage blocks for only massaging foot reflex zones, and the detachably installed foot acupuncture point massage posts are arranged on the detachably installed foot reflex zone massage blocks; the foot massage physiotherapy plates disclosed by the disclosure are safe, reliable, convenient, effective, comfortable and health-promoting.

Abstract: A film for a liquid packaging container, comprising at least one of a layer containing a resin composition (X) containing a polypropylene resin (a) and at least one of a hydrogenated block copolymer (b), the hydrogenated block copolymer (b) being a hydrogenated product of a block copolymer containing a polymer block (A) mainly containing an aromatic vinyl compound unit, and a polymer block (B) mainly containing an isoprene (Ip) unit, a butadiene (Bd) unit, or isoprene (Ip) and butadiene (Bd) units, in the resin composition (X), the hydrogenated block copolymer (b) having a phase separation structure having formed therein both (i) an island phase having a long axis of 1 ?m or more, or a bicontinuous structure, and (ii) an island phase having a long axis of 300 nm or less, and in the resin composition (X), the mass ratio ((a)/((a)+(b))) of the polypropylene resin (a) and the hydrogenated block copolymer (b) being from 61/100 to 95/100.

Abstract: A multi-vial dispensing cassette provides serial dispensement into a plurality of dispense vials. Needle holders may be provided for one or more vials in the cassette and at clip may be incorporated into the needle holder.

Abstract: The present invention relates to a medical device connector for connecting a piercing device, with a vial comprising a base member. A plurality of grip members, each grip member comprising a distal end (D) and a proximal end (P) and each comprising a wedge portion adapted to temporarily or permanently lock the medical device connector to the vial. The base member further comprises a plurality of flanges, wherein the proximal ends (P) of the grip members are arranged to the flanges. The flanges extend substantially out from the periphery of the base member in a direction substantially perpendicular to the direction of the grip members, wherein the space formed between the flanges of the base member forms at least one grip portion. The present invention provides for a medical device connector which is easy and comfortable to use, which provide good stacking capabilities and which permits a user to readily acknowledge that the medical device connector is correctly assembled with the vial.

Abstract: Provided are a method of and an apparatus for formulating a multicomponent drug capable of surely making a multicomponent drug meeting criteria for productization with high accuracy into a product. The method and apparatus obtain a chromatogram from an extract or a base of a multicomponent drug, evaluate whether the base meets the criteria for productization based on the obtained chromatogram with high accuracy, and subject the base determined in the high-accuracy evaluating as an accepted one meeting the criteria to dosage form processing, to produce a formulated drug having a given dosage form. The high quality evaluation is realized by performing peak assignment of a target fingerprint obtained from a chromatogram to a reference fingerprint with high accuracy.

Abstract: Methods and devices for exchanging therapeutic agents, such as cells, from one liquid medium to another liquid medium are provided. Aspects of embodiments of the methods include transferring a therapeutic agent from a first medium, such as a freezing, storage or shipping buffer, into a second medium, such as a sterile physiologically compatible buffer. In certain aspects, the transfer of the therapeutic agent from a first medium to a second medium involves the use of acoustic-focusing, or acoustophoresis. Embodiments of the subject methods may facilitate the transfer of a therapeutic agent from a storage medium to an infusion medium, and in certain embodiments include administering the therapeutic agent contained in the infusion medium to the subject. Also provided by the present disclosure are devices for practicing the subject methods.

Abstract: Methods, systems and apparatuses are provided for producing delivery devices, preferably for oral intake of an agent. In the broadest aspect, the method comprises assembling one or more layers comprising one or more materials with an agent or an agent-releasing formulation to form an intergraded, preferably laminated device; folding said integrated delivery device to form a folded integrated delivery device; and at least partially enclosing said folded delivery device to a form suitable for oral delivery. Preferably, the integrated device comprise a first external layer of a first material; a frame of a second material mounted on the first external layer; an agent-releasing formulation housed within the frame; and a second external layer of the first material mounted on the frame.

Abstract: The invention relates to two different patches to be applied to a person's skin, namely a hydrogel patch and a dermal patch. The patches are preferably used in combination. A particularly preferred use of the patches is the post-treatment after tattooing. The patches' ingredients do not interact with the pigments used for tattooing and therefore the patches allow maintaining the color saturation of a tattoo.

Abstract: The invention relates to a dental device and an edible pet chew. The dental device comprises a dental protection composition containing at least one barrier material, at least one activated phosphatidylcholine, and, optionally, mineral oil. The edible pet chew comprises a dental protection composition, gelatin, and, optionally, one or more humectants, one or more preservatives, one or more structure-providing components, and one or more flavoring ingredients, wherein the dental protection composition contains at least one barrier material, at least one phosphatidylcholine, and, optionally, mineral oil.

Abstract: The instant invention relates to a composition for caring for and/or making up keratin materials comprising, in a physiologically acceptable medium, at least one microcapsule containing at least one encapsulated releasable material(s) said microcapsule comprising at least one core and at least one layered coating surrounding said core, and said encapsulated material(s) being at least one reflective particle, and being only released from said microcapsule(s) when said composition is applied onto a keratin material, such as keratin fibers or skin. The invention further relates to a cosmetic process for caring for and/or making up keratinic materials, comprising application on said keratinic materials in particular on the skin of a composition as defined above.

Abstract: The present invention relates to a cosmetic composition comprising: (a) at least one anionic surfactant; (b) at least one hydrophobically-modified cationic polymer; (c) at least one water-insoluble particle comprising at least an inorganic part and/or a polymeric part and/or a visible light absorbing part; and (d) at least 40% by weight of water. The amount of the (b) hydrophobically-modified cationic polymer is preferably 0.005% by weight or more, more preferably 0.01% by weight or more, and even more preferably 0.05% by weight or more, relative to the total weight of the composition. The cosmetic composition according to the present invention can effectively deposit water-insoluble particles on the surface of various substrates such as skin and hair, and can deliver the benefits derived from the particles to the surface.

Abstract: The present invention relates to a process for bleaching or dyeing keratin fibres, in particular human keratin fibres such as the hair, comprising a step of application, to said fibres, of a composition (A) containing one or more chemical oxidizing agents and a step of irradiation of said fibres by means of UV-visible radiation having a wavelength ranging from 200 to 800 nm and a fluence ranging from 1 to 5000 J/cm2, after application of said composition (A); when the process is a process for dyeing keratin fibres, then one or more oxidation dyes is or are also used.

Abstract: The invention includes a dentifrice composition that comprises a zinc ion source, a polvphosphate ion source, an anethole, and a silica. The silica has a mean particle size of about 5 to about 12 microns, an Einlehner hardness of about 1 to about 20, and an oil absorption of about 40 to less than about 100 cc/100 g. The composition contains zinc ions and polyphosphate ions in a weight ratio of about 0.71:1 to about 10:1 and has a RDA value of about 100 to about 200 and a PCR value of about 75 to about 110. Related methods are also included.

Abstract: The present invention relates generally to methods and compositions useful for a topical composition comprising encapsulated resveratrol, oligopeptide-1, niacinamide, Opuntia ficus-indica extract, Prunus mume extract, algae extract, malachite extract, adenosine, and/or Opuntia tuna fruit extract.