Abstract: A tissue anchoring device including an expandable frame and at least one anchor having a tissue penetrating portion. The anchor is attached to the expandable frame through a plurality of beams forming a frame or a tab that enable the anchor to elastically bend with respect to a longitudinal axis of the expandable frame.

Abstract: A spine force modulating assembly for supporting a human spine that prevents, slows down, and or treats spine-related disorders. The spine force modulating assembly includes a frame of a length proportional to a distance between a third thoracic spine bone and a first sacral spine bone of a spine of a wearer of the spine force modulating assembly. The frame is of a “S” shape and configured to support a spine portion between the third thoracic spine bone and the first sacral spine bone. The spine force modulating assembly further includes a pair of shoulder straps extending from near the upper end of the frame and a pair of waist straps extending from near the lower end of the frame.

Abstract: The present disclosure provides a wearable garment comprising (a) a sheath having a first end and a second, wherein the sheath defines a cavity in a wearable position, wherein the sheath has a first opening at the first end, and wherein the sheath comprises a first material, and (b) one or more relief zones coupled to the sheath, wherein the relief zones comprise a second material, wherein a pressure distribution of the second material is greater than a pressure distribution of the first material.

Abstract: A method of detecting ostomy effluent leakage in an ostomy appliance is provided. The method includes the steps of providing a plurality of sensors; measuring resistance of the ostomy appliance using each of the plurality of sensors; entering resistance measurements in a ring buffer configured to hold resistance measurements; calculating a median resistance value of each of the plurality of sensors using the resistance measurements; comparing the median resistance value against a predetermined range of acceptable resistance values; increasing a leak count for a corresponding sensor when the median resistance value of the sensor is outside the predetermined range of acceptable resistance values; determining a leak state when the leak count increases beyond a predetermined acceptable leak count; and sending an alert upon a determination of a leak state.

Abstract: A drainage bag system for urinary collection includes a urinary drainage bag having a first inlet and an inlet valve for regulating a flow of urine from a catheter into the urinary drainage bag via the first inlet, an outlet, and an outlet valve for regulating a flow of urine out of the urinary drainage bag. The drainage bag system further includes a receptacle bag of a foil or sheet material for emptying the urinary drainage bag and having a receptacle compartment for storing urine and a connector for providing a connection between the receptacle bag and the urinary drainage bag. The connector provides a second inlet constituting a receptacle inlet to the receptacle compartment when connected to the receptacle bag such that urine can flow into the receptacle compartment.

Abstract: An ostomy pouch has a body side wall and a distal side wall defining a collection chamber. An opening is provided in the body side wall. A barrier is operably mounted to the body side wall over the opening. The barrier has an inlet opening. An internal collection member is mounted to the barrier. The internal collection member includes a tubular net having a first open end and a second closed end, and a ring-shaped capsule for storing the net inside the capsule in a collected manner. The ring-shaped capsule has an open central region and is mounted to the barrier with the capsule open central region and the barrier inlet opening aligned with one another to define a pouch inlet. The capsule extends into the pouch collection chamber and the first open end of the net is mounted to the capsule overlying the pouch inlet. Excretion is inlet to the pouch and is discharged into the net, paying out the net.

Abstract: A convex ostomy barrier includes a skin barrier, an inlet opening for receiving a stoma, and a convex insert. The convex insert includes an inner flange, an outer flange, and a middle portion arranged therebetween. The middle portion includes a pouch side surface for attaching a flange, a core-out portion configured to improve the flexibility of the convex insert, and a skin barrier support structure for supporting the skin barrier.

Abstract: An asymmetric multilayer film for an ostomy pouch includes a barrier layer including a first side and a second side. At least one layer is arranged on the first side of the barrier layer, and at least one layer arranged on the second side of the barrier layer, in which the combined thickness of the at least one layer arranged on the first side of the barrier layer is at least two times greater than the combined thickness of the at least one layer arranged on the second side of the barrier layer. The asymmetric multilayer film has a thickness of about 25 ?m to about 50 ?m.

Abstract: An ostomy barrier appliance for attaching an ostomy appliance to peristomal skin surrounding a stoma is provided. The ostomy barrier appliance includes a skin barrier, an inlet opening for receiving a stoma, and a convexity adjusting device arranged adjacent the skin barrier. The convexity adjusting device is configured to adjust the convexity of the skin barrier.

Abstract: A customizable mandibular advancement device for use in treating snoring and obstructive sleep apnea is provided. The device comprises upper and lower trays adapted to be fitted to a person's maxillary and mandibular arches. The upper tray comprises a stop member, which when engaged with a fin located on the lower tray, inhibits the posterior movement of the user's mandible thereby maintaining the mandible in an advanced position. Both the upper and lower trays comprise a core that is overmolded by a thermoplastic material that has a much lower softening temperature than the core.

Abstract: An assembly for gluteal cleft moisture reduction including a case having a plurality of walls, the case being opened by an air input port; an air tube having upper and lower ends wherein the tube's upper end forms a dorsal extension communicating with an opening in the flexible skin contact plate mounted on the case, the plate ventrally overlying the air tube; an air conduit housed within the case, the conduit having input and output ends communicating with the case's air input port and with the air tube; an electric motor and air impeller combination housed within the case, the combination being adapted for moving air through the air conduit; an electric battery within the case; and a matrix of electric conductors operatively interconnecting the electric motor and the electric battery.

Abstract: A temperature treatment apparatus includes a body made from a flexible and expandable material for attachment to a predetermined region of the human body requiring treatment with the body having a space formed therein, and a temperature radiating element shaped to be received within the space of the body and being configured to have a soft and malleable shape profile to apply temperature treatment to the predetermined region of the human body. The temperature radiating element includes an inner pouch containing a first phase change material that is able to be inserted within an outer pouch having a second phase change material, so that, upon insertion, the inner pouch is substantially encapsulated within the second phase change material of the outer pouch.

Abstract: The present invention provides improved devices for removing energy and fluid from body fluid containing spaces and surfaces of a mammal, and new uses for such devices, including fluid removal, energy removal, increasing metabolic rate; promoting weight loss; preventing esophageal burn-through, reducing beta-amylase accumulation in the brain, delaying or inhibiting the onset of Alzheimer's and other senile dementia.

Abstract: A device includes a frame, a rotatable housing and a permanent magnet. The frame is configured to be worn adjacent an eye region of a wearer. The rotatable housing is coupled to the frame. The permanent magnet is coupled to the rotatable housing and includes a first surface having a first static magnetic polarity and a second surface having a second static magnetic polarity opposite the first static magnetic polarity. The rotatable housing is arranged to rotate the permanent magnet between a first position orienting the first surface towards the eye region of the wearer and a second position orienting the second surface towards the eye region of the wearer. Related apparatus, systems, techniques and articles are also described.

Abstract: Devices, systems and methods for applying a bioadhesive substance to an internal surface of the eye, such as the retina, can include an outer sleeve having a proximal end, a distal end, a passageway extending along a length of the elongate body and an opening at the distal end of the elongate body, an applicator tip including an elongate body having a proximal end and a distal end, an applicator portion coupled with the distal end of the elongate body, and a substance supply lumen extending along a length of the device through which a bioadhesive substance can pass so that the bioadhesive substance can be applied to at least the applicator portion of the applicator tip. Some embodiments of the device can also have a source of the bioadhesive substance in fluid communication with at least the substance supply lumen.

Abstract: A tissue removal device includes a hollow needle, an ultrasonic transducer for mechanically vibrating the needle, an aspiration line communicating with the needle, and a vacuum pulsing device for generating vacuum pulses in the needle. The device may be utilized for breaking up tissue by phacoemulsification, vacuum pulsing, or both.

Abstract: Disclosed is a handheld laser probe for laser thermal conjunctivoplasty, the handheld laser comprising: a forceps; and a line focused laser light source coupled to the forceps, wherein the forceps are configured to grasp a conjunctival fold and hold the fold in a light beam of the line focused laser, and wherein the line focused laser beam is configured to uniformly heat the conjunctival fold held in the forceps. Disclosed are systems for laser thermal conjunctivoplasty including the handheld laser. Disclosed are methods of conjunctivoplasty using the handheld laser probe.

Abstract: A laser eye surgery system includes a computer which scans a focused laser beam in a trajectory over a reticle or target and determines beam quality via laser light reflected from the target. The target may have a grid pattern of lines, with the diameter of the focused laser beam determined based on a time interval for the scanned beam to move onto a line of the grid pattern. Methods for measuring beam quality in a laser eye surgery system provide a direct, quantitative quality measurement of the focused laser beam, and may be performed quickly and automatically. Using scanning mirror position information together with signals resulting from laser light reflected from the target, the laser eye surgery system may also be calibrated.

Abstract: A system for supporting and aligning a patient during a color alteration procedure includes a laser system that delivers a laser in a first direction. A control computer may be adjacent the laser system for controlling the laser system. The control computer system may include a user interface in a first plane substantially perpendicular to the first direction. The system may include a patient support structure having a patient support surface extending in a second direction substantially perpendicular to the first direction and configured to be adjustable to set a patient position or alignment relative to the laser system. Coarse adjustment hardware may be configured to cause automated and/or manual adjustments to the patient support surface in the first direction. Fine adjustment hardware may be configured to cause automated fine adjustments to the patient support surface in the first direction based on instructions received from the control computer.

Abstract: An ophthalmic laser treatment delivers patterned laser energy to an eye of a patient. A pattern-scanning laser device of the laser treatment system includes a laser module, a scanning module and delivery optics. The laser module generates laser energy (e.g. via a green laser diode), which is directed to the scanning module via a fiber optic cable. The scanning module produces the patterned laser energy by reflecting the laser energy into the delivery optics at different angles via a dielectric MEMS scanning mirror. The delivery optics includes an F-theta lens, a motorized and wirelessly-controlled spot-size selector module, and a focusing lens. A mobile computing device receives parameter information via a graphical user interface or voice control and sends the parameter information to the pattern-scanning laser device. In response to receiving activation signals from an activation unit, the pattern-scanning laser device emits the patterned laser energy based on the parameter information.

Abstract: A microsurgical device and methods of its use can be used for treatment of various conditions including eye diseases, such as glaucoma, using minimally invasive surgical techniques. A dual-blade device can be used for cutting the trabecular meshwork (“TM”) in the eye. The device tip provides entry into the Schlemm's canal via its size (i.e., for example, 0.2-0.3 mm width) and configuration where a ramp elevates the TM away from the outer wall of the Schlemm's canal and guides the TM to first and second lateral elements for creating first and second incisions through the TM. The dimensions and configuration of the blade is such that an entire strip of TM is removed without leaving TM leaflets behind and without causing collateral damage to adjacent tissues.

Abstract: A microsurgical device and methods of its use can be used for treatment of various conditions including eye diseases, such as glaucoma, using minimally invasive surgical techniques. A device can be used for cutting the trabecular meshwork (“TM”) in the eye. The device tip provides entry into the Schlemm's canal via its size (i.e., for example, 0.2-0.3 mm width) and configuration where a ramp elevates the TM away from the outer wall of the Schlemm's canal and guides the TM to first and second lateral elements for creating first and second incisions through the TM. The dimensions and configuration of the device is such that an entire strip of TM is removed without leaving TM leaflets behind and without causing collateral damage to adjacent tissues.

Abstract: A patient handling apparatus includes a patient support surface, a base, and a hydraulic circuit. The hydraulic circuit includes a pump, a fluid reservoir, and a hydraulic cylinder operable to selectively raise or lower the patient support surface or the base. The hydraulic circuit controls flow of fluid between the cylinder and the fluid reservoir to thereby control the movement of the base or patient support surface. In addition, the hydraulic circuit may include a manual bypass circuit configured to bypass the pump in response to a manual input, which allows manual extension or retraction of the cylinder, for example, when the pump is not operational. The hydraulic circuit may also include a pump bypass circuit configured to bypass the pump to allow fluid to discharge from the cap end to the fluid reservoir for faster evacuation of fluid from the cylinder, thereby increasing retraction speed of the rod.

Abstract: An isolation apparatus for the transport of a patient who is potentially infectious, who has been subjected to chemical or biological agents, such as SARS-CoV-2, or who is threatened by chemical/biological attack. The invention comprises a transparent or semi-transparent, generally tubular enclosure, having two opposite ends. Secured to each of the two opposite ends of this transparent or semi-transparent, tubular enclosure are a pair of end walls. Pass-through ports are provided to allow for introducing items, such as medicine, water, or medical tools, into the patient chamber without opening the apparatus.

Abstract: A system for supporting or positioning a patient before, during, or after a medical procedure can include a platform configured to support at least a portion of a patient. A support column can be positioned beneath the platform. A base can be positioned beneath the support column and configured to support the support column. The base can include at least one drive wheel configured to contact a ground surface and move the platform with respect to the ground surface. A drive assist user interface module can be operatively connected to the at least one drive wheel. The drive assist user interface module can be configured to permit an operator of the system to selectively control movement of the at least one drive wheel. The drive assist user interface module can be part of or be attached to an attachment that includes a plate having a top surface.

Abstract: An external automotive condenser and light assembly for mounting on a body of a vehicle, the condenser and light assembly includes a condenser housing having a top portion defining at least one top opening and a bottom portion defining at least one bottom opening. The condenser housing includes a front face so as to permit at least one warning light to be affixed thereto. The condenser housing includes a right face extending rearward from the front face. The condenser housing includes a left face extending rearward from the front face. At least one warning light is affixed to an exterior of the front face.

Abstract: A deployable gurney lift assembly 12 having a carriage assembly 14 composed of a carriage assembly plate 20 with two pivot carriage arms 38 disposed opposite one another to engage the sides of a gurney G, at least one safety bar holder 16 to accommodate a safety bar B of the gurney G, the safety bar holders 16 with at least one bar latch 18 to receive and secure a gurney bar B therein. At least one lift actuator 88 lifts and lowers the arms 38.

Abstract: Systems and methods of wheelchair systems having a companion control mode are disclosed. The wheelchair system includes a companion and a wheelchair. The wheelchair includes one or more wheels, at least one actuator coupled to the one or more wheels, a processing device, and a non-transitory, processor-readable storage medium in communication with the processing device. The non-transitory, processor-readable storage medium includes one or more programming instructions that, when executed, cause the processing device to determine the companion, generate a companion profile based on the determined companion, determine a movement of the companion, and actuate the at least one actuator to drive the one or more wheels to follow the movement of the companion. The actuation of the at least one actuator to drive the one or more wheels to follow the movement of the companion is an autonomous control.

Abstract: An apparatus for reorienting a person includes a wrap having a first lateral portion and a second lateral portion, the first lateral portion and the second lateral portion being releasably securable to one another along an anterior region of the wrap between lateral sides of the person and along a posterior region of the wrap between the lateral sides of the person via a set of fasteners. Each of the lateral portions are dimensioned to extend around a corresponding one of the lateral sides of the person and having anterior and posterior edges that are dimensioned to extend at most partway across to an opposite one of the lateral sides of the person. The wrap is made from flexible materials and dimensioned to extend at least from below knees of the person to above the elbows of the person and snugly retain the person therein.

Abstract: Disclosed is a therapeutic stretching apparatus, which in particular provides a user with a system for providing an assist to increase knee extension as well as for maintaining stability of the knee after surgery. This device can not only act as a therapeutic stretching apparatus but also can act as a primary post-op knee brace with locks/limits on hinge to prevent user from further injuring the joint.

Abstract: An inversion table includes a supporting stand, a tilt inversion mechanism and an operating unit. The tilt inversion mechanism includes an inversion unit including a support table assembly which is pivotally disposed on the supporting stand, and an extension assembly which is coupled with and extends from the support table assembly downwardly. A feet holding unit includes a front feet holding assembly securely and non-pivotably disposed on a lower portion of the inversion unit, and a rear feet holding assembly pivotably and movably connected to the inversion unit. The operating unit includes an operating assembly operably coupled with the front feet holding assembly, and is rotatable about a rotating axis at the front feet holding assembly to actuate the rear feet holding assembly to rotate and move toward the front feet holding assembly. In an inversion state, the users feet is firmly held on the front feet holding assembly.

Abstract: A method and system for implementing an exercise protocol for osteogenesis and/or muscular hypertrophy are disclosed. A method may include initiating, based on the exercise protocol, a warmup session for a first exercise, where the warmup session specifies applying a first target load threshold for a first period of time. The method includes determining the warmup session is complete after the first period of time elapses. Responsive to determining the warmup session is complete, the method includes initiating, based on the exercise protocol, a resting session specifying not applying loads for a second period of time. The method includes determining the resting session is complete after the second period of time elapses. Responsive to determining the resting session is complete, the method includes initiating, based on the exercise protocol, an exercise session specifying applying a second target load threshold for a third period of time.

Abstract: A male stimulation apparatus, comprising: a housing defining a hand tunnel extending in a lateral direction and defining at least one hand hole to facilitate an entry of a hand of a user inside the hand tunnel; a phallus tunnel extending inside the housing from a first longitudinal end towards a second longitudinal end, the phallus tunnel extends through the hand tunnel and is adapted to receive a phallus of the user; and a vibrator shaft extending inside the housing from the second longitudinal end towards the first longitudinal end, the vibrator shaft extends through the hand tunnel and is adapted to receive a vibrator, wherein the hand tunnel facilitates the user to grasp the phallus tunnel and the vibrator shaft.

Abstract: A male sexual stimulation device that provides a better user experience by combining a mechanical stroking mechanism with a spiraling sleeve that provides rotational stimulation and suctional stimulation to the stroking motion of the mechanical stroking mechanism. The spiraling sleeve is formed at least in part from an elastomeric material with ribbing molded into the interior of the sleeve at an angle to the linear axis of the spiraling sleeve such that elongation or shortening of the spiraling sleeve along the linear axis with a penis inserted therein causes a portion of the sleeve to twist about the linear axis.

Abstract: A manipulator for a massage device includes a pair of main rods having a first end pivotably coupled to a first elbow assembly and a second end opposite the first end that is pivotably coupled to a second elbow assembly. The pair of main rods is transitionable between a first configuration and a second configuration, wherein, when in the first configuration the pair of main rods define a first length and when in the second configuration the pair of main rods define a second length greater than the first length. The manipulator further includes a first arm rod pivotably coupled to the first elbow assembly, and a second arm rod pivotably coupled to the second elbow assembly.

Abstract: A garment assembly includes a sleeve member having outer and inner surfaces, a first vibration assembly associated with the sleeve member, and a control module associated with the sleeve member. The first vibration assembly includes a plurality of vibration motors that are arranged in a circle about a center point. An angular distance between each vibration motor of the plurality of vibration motors is approximately the same. The control module includes a battery, and the first vibration assembly is in electrical communication with the control module.

Abstract: A CPR chest compression system includes a retention structure that retains the body of a patient, and a motor and a compressor that can perform CPR compressions to the chest of the patient. The motor is powered by a battery that is located on the retention structure but away from the motor, and is electrically connected to the motor via one or more wires. Accordingly the weight and volume of the battery can be located away from a top portion of the retention structure. This renders the CPR system is less heavy at the top, and therefore less likely to tilt and start compressing the chest at a different point. Moreover, this permits X-Rays of a larger footprint to go through the CPR system and reach the patient, in example configurations where the components are transparent to X-Rays.

Abstract: Sauna heaters are used to generate heat for saunas. Sauna heaters include a first halogen tube configured to generate heat, a second halogen tube configured to generate heat, wherein the first halogen tube is implemented a distance from the second halogen, and wherein the distance between the first halogen tube and the second halogen tube is configurable to adjust an amount of electromagnetic field (EMF) emitted by the heater. Sauna heaters also include a source of alternating current electrically coupled to the first halogen tube and the second halogen tube such that the source of alternating current is configured to provide the first halogen tube and the second halogen tube with a current, wherein the current powering the first halogen tube is out of phase with the current powering the second halogen tube.

Abstract: A floating physical therapy device includes a frame and a harness. The frame includes an inner frame and an outer frame on the right and left side. The inner frame defines a patient area. The harness is attached to the inner frame such that it secures a patient to the device in a substantially upright position during use. The frame extends forwards and backwards, as well as to the left and right, of the patient area in order to provide stability in the water during normal use. The frame defines a trainer area immediately forward of the patient area where a therapist can have access to the patient during therapy sessions.

Abstract: A seat device includes a massage mechanism configured to massage a first muscle and a vibration generation mechanism configured to administer a vibratory stimulus having a frequency that causes muscle tone to a second muscle, the second muscle being an antagonist muscle of the first muscle.

Abstract: A pill container includes a base with a cavity and a lid movable between a closed position and an open position. The base has an integral spring tab such that when the lid is unlocked from the base, the spring tab pushes against an interior part of the lid to move the lid from the closed position to the open position.

Abstract: A medication information and storage device that provides easy, on-hand, transportation and storage of medication and information regarding a health condition for which the medication may, in an emergency, stop or limit certain, possibly life-threatening, symptoms. The device includes a card with printed information, such as symptoms, treatments, and how to best take accompanying medication, and a cavity containing medication disposed in a corner of the card. In use, the device is carried upon a person, such as in a wallet, retrieved and read by a person when experiencing a health condition, and opened to provide medication for the health condition, if the person believes after reading the information that taking the medication may help.

Abstract: A continuous skin packaging and coating apparatus and a coating method for tablets. The continuous skin packaging and coating apparatus comprises a lower coating film unreeling roller, a waste edge reeling roller, an upper coating film unreeling roller, a lower coating film heating component, an upper coating film heating component, a first mold provided with a first tablet placing hole, a second mold provided with a second tablet placing hole, a heat-sealing plate, a cutting component, a blank tablet implanting component, and an operating mesa. The lower coating film unreeling roller and the waste edge reeling roller are provided on either side of the operating mesa. The lower coating film heating component, the blank tablet implanting component, the upper coating film unreeling roller, the upper coating film heating component, the heat-sealing plate, and the cutting component are sequentially provided above the operating mesa.

Abstract: Disclosed herein are modular container systems having child-resistant containers, tray inserts and tray frames. Also disclosed are methods using the modular container systems and methods of storing substances in containers. The containers have a container base and a container cap and provide for child-resistant containers. A user can releasably remove the container cap from container base with a squeeze and lift sequence. For example, the user squeezes opposite sides of the container base, which releases a locking mechanism and allows for removal of the cap by lifting or pulling the container cap off from the container base. The components of the modular container system are modular and stackable. The modular system allow for organized, efficient, accessible and storage of the child-resistant containers. The modular container system also allows for easy counting, sorting and processing of the containers.

Abstract: A system for dispensing and compounding errors prevention is disclosed. The system for dispensing and compounding errors prevention comprises at least one camera for receiving a real-time image of personnel preparing a prescription; a data storage for storing a medication recipe of a corresponding patient; an identification module for determining an identification tag of a drug from a container of the drug or a physical appearance of the drug; a measurement module for determining an amount of the drug being dispensed by the personnel; a comparison module in communication with the identification module and the measurement module for determining whether the amount of the drug being dispensed by the personnel or the identification tag of the drug match the medication recipe; and an output device for outputting a notification to the personnel.

Abstract: Disclosed is an invention for dispensing multiple medications to a patient over an extended period of days up to several times a day. The system includes a carousel with storage bins and a delivery bin on its periphery. A vacuum system and a vacuum probe with a vacuum cup at the end of the probe for grasping and holding by an induced vacuum a dosage of medication located in a storage bin and moving it to a dispending or delivery bin. The system includes a programmable computer to control the system and sequence the proper dispensing of the medication at the predesignated times.

Abstract: A method for loading a medicine transport plate with one or more medicine items using a docking station includes the steps of moving a preparation release mechanism of a docking station into a preparation holding state; inserting the one or more medicine items into one or more preparation compartments in the docking station; loading the medicine transport plate into the docking station; and moving the preparation release mechanism from the preparation holding state into a preparation release state to release the one or more medicine items from the preparation compartments.

Abstract: The present specification provides improved methods of treating Her2+ cancers in which an RXR agonist and a taxane are administered to a subject having a Her2+ cancer. Thyroid hormone and other anticancer agents may also be administered. Related compositions and combination are also disclosed.

Abstract: The present disclosure provides methods of treatment using ophthalmic compositions comprising semifluorinated alkanes for keratoconjunctivitis sicca and/or Meibomian gland dysfunction, which methods provide for the enrichment of an ophthalmic tissue in the semifluorinated alkane, and optionally methods of delayed release of the semifluorinated alkane from the enriched ophthalmic tissue to the surface of the cornea and/or conjunctiva, and/or to the Meibomian gland.

Abstract: A treatment regime for use in the treatment or prevention of dermatitis and inflammatory skin conditions, said regime comprising the administration of: a) between 50 mg and 3000 mg of a topical liquid or gel composition comprising between 1% w/w and 15% w/w cannabinoid, wherein the cannabinoid is dissolved in the liquid or gel composition.