Abstract: A male chastity system comprises a housing and a partial ring configured for placement behind the scrotum of the user. The partial ring contains a gap. A bridge bridges the gap by attaching to the partial ring at first and second attachment points. The bridge comprises a rear portion and a front portion, and the partial ring and the bridge collectively form a ring. Guide pins extend at least partially through the rear bridge portion, attachment points, front bridge portion, and housing. A locking pin extends through the bridge and housing, a spacer on the locking pin spacing the housing from the ring, and a lock is applied to the locking pin.

Abstract: An orthopedic device in the form of a circumferential walker includes a first member (posterior shell) and a second member (dorsal shell) corresponding to the first member. An outsole or plantar shell portion is attached to, or formed on or with the posterior shell. An expansion joint is positioned in the posterior shell or dorsal shell to expand to accommodate larger sized lower legs. The dorsal and posterior shells may include flexible or resilient edge portions to reduce pressure points and to further accommodate users having larger sized lower legs. The dorsal shell also includes a flexible or resilient connecting portion to accommodate users having larger ankles and feet and to reduce or eliminate the formation of a pressure point along the dorsal shell. Quick-connecting buckle assemblies can be provided to allow a user to quickly don and doff the orthopedic device.

Abstract: A veterinary anesthesia monitor system useful in establishing, maintaining, and reporting upon the anesthesia gas mixture delivered to or exhaled by a patient.

Abstract: Methods and devices are disclosed for manipulating the airway, such as to treat obstructive sleep apnea. An implant is positioned within the body with respect to the airway. The spatial orientation of the airway is manipulated, directly or indirectly, to affect the configuration of the airway. In general, the implant is manipulated to displace the trachea in an inferior direction, resist superior displacement of the trachea and/or to alter the tracheal wall tension. The implant restrains the trachea in the manipulated configuration.

Abstract: A method of forming a fenestrated extremity surgical drape includes providing improved seal integrity to reduce the occurrence of pathogenic contamination at the surgical site via migration through the seal. The seal has a non-linear configuration to eliminate uneven stress concentrations commonly located at the corners of rectilinear seals. An elastomeric apertured panel can be disposed between a film panel and a fiber/film laminate panel. These layers can be joined by a heat sealing operation along two spaced apart concentric seal locations ringing the aperture and a fenestration in the laminate panel. The assembly can then be affixed by adhering the underside(s) of one or more panels to a base drape, which has an opening aligned with the aperture and fenestration.

Abstract: In order to prevent tainting of a cougher's hand with germs, the product from a cough is carried in contact with a germicide inside a hollow article, and is vented out of the hollow article, in directions away from the user's face and hand holding the article. More specifically, the cough catcher has a hollow region for accepting the product from a cough therein. This hollow region has a filter element containing a germicide mounted therein, and a series of channels formed between the filter element and a bottom surface of the hollow region. The channels communicate with vent ports around a rim portion of the cough catcher. The vent ports are oriented away from both the mouth opening and the outside surface of the cough catcher for conveying the product from a cough away from both the face and the hand of a user.

Abstract: An apparatus and methods for treating sleep apnea and/or snoring are provided. The apparatus includes an appliance sized and structured to be placed in the pharyngeal region of a human or animal. The appliance, when so placed is effective in treating sleep apnea and/or snoring, for example in maintaining openness of an oropharyngeal region of a human or animal during natural sleep. Preferably, the appliance is non-circumferential in form and includes rounded, spaced apart end portions.

Abstract: A device for occluding the fallopian tube including a retention member and a mesh material supported by the retention member. The retention member has a first lower profile configuration for delivery and a second expanded configuration for placement within the fallopian tube. The mesh material is configured to block passage of an egg through the tube. The member has a plurality of tube engagement members to secure the retention member to the fallopian tube.

Abstract: Disposable operating room surgical draping systems are disclosed. Methods of using disposable operating room surgical draping systems are also disclosed.

Abstract: The invention relates to a production process for a foam wound dressing having an external germ barrier, more particularly a film layer, and also to a wound dressing thus obtained, having, where appropriate, a pressure-sensitive adhesive layer. In the process according to the invention the germ barrier is produced by means of extrusion directly on the foam base. This results in a more reliable bond between foam layer and germ barrier, without detriment to the absorptiveness of the foam for wound exudate. The process presented is simple and cost-effective, and all of the requirements from the medical sector (e.g. absence of solvent) can be met.

Abstract: Methods and devices are disclosed for manipulating the tongue. An implant is positioned within at least a portion of the tongue and may be secured to other surrounding structures such as the mandible and/or hyoid bone. In general, the implant is manipulated to displace at least a portion of the posterior tongue in an anterior or lateral direction, or to alter the tissue tension or compliance of the tongue. Methods and devices are also disclosed for manipulating other soft tissue structures, including the soft palate and pharyngeal airway.

Abstract: Described here are devices for altering the flow of air in a respiratory cavity such as the mouth and nostrils of the nose. These methods and devices may be useful for affecting a physiologic benefit in patients suffering from a variety of medical diseases, particularly those that may benefit from “pursed-lip” breathing and non-invasive ventilation, such as COPD, heart failure, sleep apnea, and other medical disorders. The devices are typically removable devices that may be placed over or in a respiratory cavity to increase resistance to airflow within the respiratory cavity. Resistance to expiration may be selectively increased relative to inspiration. Removable oral and removable nasal devices are described. Oral and nasal devices that filter inhaled airflow of debris and allergens are also provided. A nasal device that increases patency of the nares is also provided.

Abstract: A liquid evaporator includes a liquid reservoir (3) with a liquid to be evaporated, a heater (9) and an evaporator tube (12). The evaporator tube (12) has a first porous element (1) having a first porosity and with an area in contact with the liquid in the liquid reservoir (3) and a second porous element (2) with a second porosity and with an area present on an evaporator side (50) used to dispense the evaporated liquid, and an area outside the liquid reservoir heated by the heater (9) which is not directly in connection with the liquid. The first porous element and the second porous element are in contact in contact areas with the first porous element forming a wick delivering liquid from the reservoir to the contact area.

Abstract: A method and a CPAP apparatus for characterizing different mask systems, e.g., masks and hoses, are provided. The apparatus can be calibrated for different mask systems and hoses by including sensors for measuring flow and pressure at a flow generator of the apparatus. When the flow generator is fitted to a new system, or changes are made to an existing system, mask or patient interface, and/or hose, a method of calibrating the flow generator is provided. The method includes determining air flow characteristics of the hose using flow measurements made during a first test period when flow through the system is open, measuring or estimating pressure in the system during a second test period when flow through the system is blocked, and determining air flow characteristics of the diffuser using the air first test period flow characteristics of the air delivery hose and the second test period pressure measurements.

Abstract: An infant nasal interface prong device for use with an nCPAP system. The device includes first and second nasal prongs and a base. Each prong includes a bellows segment, a tip, and a lumen. The tip extends from the bellows segment to a tip end and is adapted for insertion with an infant's naris. The lumen extends through the tip and the bellows segment. In an undeflected state, a central axis of the lumen along the bellows segment is transversely offset from the lumen axis at the tip end. The base is connected to each of the nasal prongs and is adapted for coupling to a CPAP generator. The bellows segment renders the corresponding prong highly flexible relative to the base. The offset positioning of the tip end promotes desired positioning of the base/CPAP generator, relative to the patient and more closely conforms to the expected nasal anatomy.

Abstract: A brace hosiery apparatus including a hollow, cylindrical brace covering disposed about at least a portion of an orthotic brace and a first connector that when removably connected to a second connector secures the brace covering to the orthotic brace.

Abstract: An adjustable support assembly for an orthopedic brace has a support bar, a housing and a locking mechanism. The housing includes a travel track which receives the support bar. The locking mechanism includes a lock stop and a lock peg array having at least one column and a plurality of rows. The lock stop is perpendicularly positioned between two lock pegs in adjacent rows to prevent displacement of the support bar in the travel track when the length locking mechanism is in the closed position and the lock stop is parallely positioned to enable displacement of the support bar in the travel track when the length locking mechanism is in the open position.

Abstract: A mandibular protrusion device includes an upper dental tray to be placed on the upper dental arch of a patient and a lower dental tray to be placed on the lower dental arch, as well as two lateral links for connecting both trays in order to advance or draw back the lower dental arch during a vertical movement between both dental arches, each lateral link including an element of traction attached to the trays via its ends. Each lateral link includes ball pivots having an opening for receiving an end of an element of traction, and each tray includes two lateral seats for accommodating a ball pivot connected to an element of traction so that the lateral links are connected to the trays via a ball pivot joint. A corresponding lateral link and a method for assembling the mandibular protrusion device are also disclosed.

Abstract: The present invention discloses a pivotal disc is pivotally coupled to a first brace and a second brace. The pivotal disc has a motion-limit member and a positioning member limiting the angle by which the second brace rotates with respect to the first brace with the pivotal disc being the axis and fixing the angle between the first and second braces. The present invention is characterized in that the motion-limit member uses a range-adjust member to push a slide block and determine the range that a block portion of the second brace is blocked by the slide block, and that the positioning member uses a switch knob actuates on end of a positioning rod to engage with or depart from a positioning notch on the pivotal disc, and that the pivotal disc has two limit elements to define the maximum movement range of the first brace and the second brace.

Abstract: A method for managing at least one breathing condition may include storing an agent near a patient's airway and delivering the agent to the mucosal tissue in the pharyngeal area in a time-released manner during a sleep period. The delivered agent may cause increased contraction of muscle tissue in the pharyngeal area.