Abstract: An ocular protection device and treatment methods are disclosed. The device has a corneal shield with an attached handle. The handle may be used to move the corneal shield to better protect the eye from various treatment modalities. The handle may also be used to place tension on the eyelid to counteract the forces imposed by a treatment handpiece. A procedure for treating the eye is disclosed where multiple passes with a treatment handpiece cause a gradual increase in the temperature of an eyelid up to a treatment temperature. Once the treatment temperature has been met, occlusions in the Meibomian glands of the eyelid may be expressed. The procedure may be repeated recursively until a desired level of expression has been achieved.

Abstract: Trimmable conformable wound dressings, kits containing the same and methods of using the same. The wound dressings may protect a treatment site from microbial contamination or other disturbances while a wound heals or to enable the application and maintenance of vacuum over the treatment site. The wound dressings may include first and second sections of support layer material on opposite sides of one or more intermediate sections of support layer material. The first and second sections of support layer material meet the intermediate sections of support layer material along peel tab junctions that provide peel tabs.

Abstract: A garment including an inflatable protective device that can include at least one inflatable bag suitable for moving between a rest condition, wherein it is deflated, and an operating condition, wherein it is inflated; an inflator unit designed for inflating the at least one inflatable bag; sensors designed for monitoring the user's body for shocks or unexpected movements; and a control unit designed for processing the data provided by the sensors and for activating the inflator unit if, on the basis of the data received by the sensors, a danger situation is identified. The garment can further include a display unit which has an alphanumeric and/or graphical visual display for providing the user with messages and/or symbols about the internal status of the inflatable protective device.

Abstract: Certain configurations of removable oral devices are described. In some instances, the removable oral device includes a palatal element. In certain configurations, the palatal element may comprise a variable hardness at different areas, e.g., edges can be softer than other areas of the removable oral device. In other instances, the removable oral device may comprise two or more individual palatal elements which together can form the palatal element and permit user adjustment of the oral volume. Various materials used in the palatal element are described. Sensors and other on-board devices are also described.

Abstract: A system for strain relieving intravenous (IV) assembly includes a dressing and an anchor portion for use with the dressing. In various embodiments, the dressing may cover an injection site into a portion of a patient's body for an intravenous (IV) assembly that provides fluid communication between the injection site and a fluid reservoir remote from the injection site through a flexible tube. In an illustrative example, the anchor portion may include a first member and a second member. The first member may be secured, for example, to the dressing and may, in some examples, wrap around the tubing so as to resist axial movement of the tubing relative to the dressing. The second member may be secured to the dressing and may wrap around the tubing and a portion of the patient's body so as to resist radial movement of the tubing relative to the body.

Abstract: An oral device may include a body. The body may have a main portion having an arch-shaped central portion, a first side portion extending from a first end of the central portion, and a second side portion extending from a second end of the central portion. The body may further include a first wedge portion provided on a bottom surface of the first side portion, and a second wedge portion provided on a bottom surface of the second side portion. Each of the first wedge portion and the second wedge portion may have a varying thickness.

Abstract: Described are embodiments of a multilaminate or multiple layer implantable surgical graft with an illustrative graft comprising a remodelable collagenous sheet material, the graft including one or more interweaving members to stitch together the graft to help prevent the layers from delaminating or separating during handling and the initial stages of remodeling. The interweaving members may comprise lines of suture, thread, individual stitches, strips of material, etc. that are woven through the layers of biomaterial in a desired pattern. In one embodiment, the interweaving members comprise a pharmacologically active substance, such as a drug, growth factors, etc. to elicit a desired biological response in the host tissue. In another embodiment, the graft further comprises a reinforcing material, such as a synthetic mesh, within the layers of remodelable biomaterial and stitched together by one or more interweaving members.

Abstract: In an embodiment, a circuit includes a resonant portion, a plurality of switches, a first impedance, an amplifier, and a demodulator. The resonant portion includes a single RF coil and is configured for transmission/reception at about the same frequency. The switches include first, second, and third switches. The first switch includes an input in communication with a power source and an output in communication with ground. The second switch includes an input between the power source and the first switch and an output in communication with a resonant portion input. The third switch includes an input in communication with a resonant portion output and an output in communication with ground. The first impedance is between the resonant portion output and the third switch input. The amplifier includes an input between the first impedance and the third switch input. The demodulator includes an input in communication with the amplifier output.

Abstract: The present invention discloses a negative-pressure oral apparatus capable of relieving discomfort of soft tissues in the oral cavity and improving fixation of the oral apparatus to prevent the oral apparatus from falling off due to mouth opening. The oral apparatus is compact and elastic so that it fits various shapes and sizes of the oral cavity and is easy to be put on and taken off to provide convenience and safety to the user. In another embodiment, a method for maintaining a negative oral pressure and collecting liquid by coupling the oral apparatus to a liquid collecting apparatus capable of effectively providing the oral cavity with a negative pressure to expel liquid in the oral apparatus and deliver the liquid to an absorbing element in the liquid collecting apparatus so as to prevent liquid leakage or contamination.

Abstract: A medical device or catheter management system comprises several layers where a top layer has one or more channels to receive one or more elongated medical devices or members and a bottom layer comprises adhesive to secure the catheter management system to a patient or other secure site in the operating field. A firm upper surface causes the elongated medical devices or members to stay in the channels, whereas a firm inner layer facilitates maintaining the shape of the catheter management system and providing resistance for an operator to easily release an elongated medical device or member.

Abstract: A shield system for protecting a curved object is described. The system comprises at least one flexible pad. The at least one flexible pad comprises a spacing ridge (7) projecting at an angle from a first major surface (3) of the pad for providing a spacing between the first major surface and a support ridge (9) projecting from the first major surface and extending transverse to the spacing ridge. The support ridge comprises a flexure region (11) adapted to unbend in the event that the pad is curved about an axis aligned with the spacing ridge to inhibit strain in the support ridge from causing deflection of the spacing ridge.

Abstract: A valve component (1) of the invention comprises a main valve (2) which is located on a centre line and at least one auxiliary valve (3) which is located radially outwardly of the main valve (2). The main valve may be used for sealing engagement with a cannula. In some cases the cannula may be used for introduction of a number of robotically controlled surgical instruments generally, including a camera. The auxiliary valves (3) may be utilised to introduce another instrument through the valve component. The valve component is mounted in a manner which ensures that the valve component (1) is rotatable about a centre line through the axis of the valve component (1).

Abstract: A pressure ulcer dressing assembly includes a cushion that is hollow. The cushion is curved such that the cushion has a C shape and the cushion is positionable around a pressure ulcer on a patient having the cushion partially encircling the pressure ulcer. A gel fills the cushion and the gel absorbs weight of the patient when the cushion is positioned on the patient. In this way the cushion inhibits the pressure ulcer from is exposed to pressure thereby enhancing healing the pressure ulcer. A dressing is coupled to the cushion, the dressing extends laterally across the cushion and the dressing covers the pressure ulcer when the cushion is positioned on the patient. A pair of adhesive pads is each coupled to the dressing for retaining the dressing and the cushion on the patient.

Abstract: A tongue attachment assembly includes a sheath designed for attachment to a patient's tongue using a vacuum. An accessory attachment feature comprising a groove located between a flange and the distal end of the body of the sheath. Vacuum can be drawn through a valve or an external vacuum source. The tongue attachment assembly can be adapted for any of a variety of applications by selecting an appropriate accessory and attaching the accessory to the sheath by the accessory attachment feature. Accessories can include a sleep apnea attachment, a gas delivery mask retention attachment, and the like. A tongue shape restoration device can be employed to restore the tongue from a shape that is deformed by the tongue attachment assembly to a natural shape. The tongue shape restoration device can be a pair of cantilevered arms, an orbital shaped device, or any other suitable component.

Abstract: A camera and drape assembly for use with tracking elements of a surgical system includes a camera unit and a drape covering the camera unit. The camera unit includes a casing presenting a face for facing the tracking elements. Optical sensors are supported by the casing and are exposed through the casing for detecting the tracking elements. The drape covers the camera unit such that light signals from the tracking elements can be received by the optical sensors.

Abstract: An adjustable mandibular repositioning appliance including first and second connecting members and a link arm which is pivotable about an axis wherein protrusive positioning of the mandible is provided by relative positioning of the link arm along aid axis, to kits and couplings for making a readily adjustable mandibular appliance, to a system for providing a readily adjustable mandibular repositioning appliance and methods of use.

Abstract: A surgical drape includes a seal connectable with a selected surface of a body to define a sterile region that includes access to at least two surgical approaches. A sleeve is connected with the seal and a draping is disposed with the body. The sleeve defines a cavity in communication with the region. Surgical instruments, systems and methods are disclosed.

Abstract: Trimmable conformable wound dressings, kits containing the same and methods of using the same. The wound dressings may protect a treatment site from microbial contamination or other disturbances while a wound heals or to enable the application and maintenance of vacuum over the treatment site. The wound dressings may include first and second sections of support layer material on opposite sides of one or more intermediate sections of support layer material. The first and second sections of support layer material meet the intermediate sections of support layer material along peel tab junctions that provide peel tabs.

Abstract: The present invention is disclosing protective apparel comprising a textile fabric of a defined material. Defined material includes textile clothing fiber embedded with microfilaments of a metal forming a Farady cage around a wearer. Protective apparel blocks electromagnetic and/or radio frequency field waves.

Abstract: A bandage system lances a skin tag from a person's body and thereafter projects the wound created. The system has a base layer that is adhesively attached to the person such that the skin tag passes through an opening of the base layer. A cutter is located atop the base layer and uses a pair of blades that are squeezed together to cut the skin tag protruding through the opening. After cutting, a protective layer is adhered to the base layer such that a medicine laden absorbent pad on the protective layer overlays the opening on the base layer absorbing any blood from the wound and applying the medicine to the wound. Thereafter, the system is worn as a typical bandage.

Abstract: A device for monitoring fluid leakage. A flexible plastic sheet (11) is provided with a tear-off strip (12), which divides the sheet in a first sheet portion (21) and a second sheet portion (20) and forms a folding line. An adhesive (22) is arranged at the first portion (21). The sheet is folded along the folding line and the first portion is attached to the second portion via the adhesive to form a pocket along the folding line for enclosing a connector and hose assembly to be monitored. An optical sensor having an absorbent pad and an optical fiber is enclosed in said pocket when formed. The exterior end of the optical fiber is connected to an optical detector device for monitoring if the interior end of the optical fiber comes into contact with a fluid, indicating a leakage of the connector.

Abstract: A conformable body interface is fabricated using a data set representing a three-dimensional, soft tissue body surface. The conformable body interface includes a body scaffold that is divided into two or more longitudinal segments separated by axial joints. Optionally, the body scaffold is further divided into two or more circumferentially split segments separated by circumferential joints. The axial joints are circumferentially constrained by elastic bands, tabs, or similar structures and the circumferential joints are longitudinally constrained by elastic axial tethers or similar structures. In this way, the body interfaces can accommodate swelling and bending of the body surface.

Abstract: A garment (10) including an inflatable protective device (11). The device (11) includes at least one inflatable bag (12), an inflator unit (14), sensors (17, 18), and a control unit (19). The bag (12) for moving between a rest condition, wherein it is deflated, and an operating condition, wherein it is inflated. The inflator unit (14) for inflating the bag (12). The sensors (17, 18) for monitoring the user's body for shocks or unexpected movements. The control unit (19) for processing the data provided by the sensors (17, 18) and for activating the inflator unit (14) if, on the basis of the data received by the sensors (17, 18), a danger situation is identified. The garment (10) provided with a display unit (22) which includes an alphanumeric and/or graphical visual display (24) for providing the user with messages and/or symbols about the internal status of the device (11).

Abstract: A sterilization wrap system with features for protecting a sterilization wrap and/or a sterilization tray of the sterilization wrap system is provided. Such features include strap or belt protectors, edge protectors, corner protectors, and/or expandable protectors, which each may provide protection of one or more areas of the sterilization wrap and/or tray when positioned against an outer surface of the wrap and/or between an inner surface of the wrap and a container for holding implements to be sterilized. A size-selectable protection system also is provided. The size-selectable protection system provides a material having a plurality of perforations such that a length of the material may be selected and detached from the rest of the material. The selected length of material may be used with a sterilization wrap system to protect a sterilization wrap and/or sterilization tray from cuts, tears, or the like.

Abstract: A surgical apparatus of the present disclosure includes a wound retractor having a specimen bag attached thereto. Kits of the present disclosure include the surgical apparatus and a vacuum tube. In embodiments, the vacuum tube may be introduced into a lumen of the wound retractor. A vacuum source is attached to a proximal end portion of the vacuum tube to draw a vacuum through the vacuum tube, which in turn draws a tissue specimen into the lumen of the vacuum tube through an opening in the distal end portion of the vacuum tube. The vacuum tube, possessing the tissue specimen therein, may then be removed from the wound retractor. Methods for using the surgical apparatus and/or kits of the present disclosure are also provided.

Abstract: The invention relates to a set (1) of standard or tailor-made disposable instruments for a surgical operation on a patient, said set comprising at least two components (5) connected to each other by at least one connecting tab (6), which is connected separably to said components (5).

Abstract: Systems and methods provide protection for patient tissue during radiofrequency ablation treatments. Exemplary techniques involve placing a conductive or semiconductive pad assembly near a target tissue, and administering electrical current through the target tissue while protecting adjacent tissue with the pad assembly. The pad assembly may include a material having an electrical conductivity value that is equal to or greater than the electrical conductivity value of the target tissue.

Abstract: Ophthalmic implants and methods of use that provide structural support to the optic nerve are disclosed herein. An adhesive and/or ophthalmic implant may be delivered to an optic nerve of an eye to relieve pressure on the optic nerve. The ophthalmic implant may include a base portion that includes a first surface and a second surface opposing the second surface and a protrusion from the second surface for extending into a cup of an optic nerve in an eye.

Abstract: Components, systems and kits for capturing and removing tissue from mammalian bodies include a tissue container that may be introduced into a body cavity and within which a tissue specimen may be placed, cut and removed from the body cavity. Methods of using these components, systems and kits are also described.

Abstract: A breathing system is provided which enhances the ability of a user to breathe through the user's nasal passageways. The breathing system generally includes a bridge member and a pair of nasal appliques which are attachable to the lateral portions of the user's nose. The bridge member is positionable adjacent the appliques to activate the system and impart a dilating force onto the user's nose. The system may be deactivated by removing the bridge member from the appliques, and thereby removing the dilating force from the user's nose.

Abstract: A medical apparatus for the treatment of one or more sleep disorders such as obstructive sleep apnea in a patient is provided. The apparatus has an elongate member with a middle portion, a first fixation element and a second fixation element. The middle portion applies a force to a segment of a patient's airway.

Abstract: A novel application apparatus for the proper application of makeup, including mascara, eyeliner, eye glitter, costume or stage makeup, lipstick and nail polish, and other facial makeup products, along with the proper application of adhesive for false eyelashes, among other uses. The instant disclosure relates to methods for using the apparatus for applying the makeup as set forth herein, along with a novel packaging device for the application apparatus.

Abstract: A handheld device measures all vital signs and some hemodynamic parameters from the human body and transmits measured information wirelessly to a web-based system, where the information can be analyzed by a clinician to help diagnose a patient. The system utilizes our discovery that bio-impedance signals used to determine vital signs and hemodynamic parameters can be measured over a conduction pathway extending from the patient's wrist to a location on their thoracic cavity, e.g. their chest or navel. The device's form factor can include re-usable electrode materials to reduce costs. Measurements made by the handheld device, which use the belly button as a ‘fiducial’ marker, facilitate consistent, daily measurements, thereby reducing positioning errors that reduce accuracy of standard impedance measurements. In this and other ways, the handheld device provides an effective tool for characterizing patients with chronic diseases, such as heart failure, renal disease, and hypertension.

Abstract: A sleep apnea prevention sleep-aid mask is described. The sleep-aid mask is configured to secure the lips of a user together in a natural state, in order to encourage the respiratory system of the user to employ the nasal passages rather than the mouth for respiration. A pad equipped with a perforated mesh or channel is positioned over the lips and mouth of the user, and secured in position on the user via an adhesive, which temporarily affixes the pad to the face of the user. The sleep-aid mask is preferably shaped and sized according to the specific size of the user's face, and is configured to limit the effective diameter of the mouth of the user, in order to cause continued use of respiration via the nasal passages.

Abstract: An assist garment worn on a part of a human body includes a plurality of garment-fitting actuators that are placed linearly along at least one end portion of a garment body and driven to extend and contract, a plurality of assisting actuators that are placed linearly on the garment body to cross the fitting actuators and driven to extend and contract, and a controller that individually controls the drive of the assisting actuators and the drive of the fitting actuators.

Abstract: A shield structure configured to protect a head and/or neck of a patient during a radiologic procedure comprises a bottom wall, a side wall, and an opening. The bottom wall includes radiation attenuating material and is configured to be positioned between the head and/or neck of the patient and a radiation source so as to shield the patient from radiation directed toward the bottom of the patient. The bottom wall is of a general size to shield the head and/or neck of the patient. The side wall includes radiation attenuating material and is configured to extend upward from the bottom wall so as to shield the patient from radiation directed toward a side of the patient. The opening is configured to receive the head and/or neck of the patient.

Abstract: A Multi-sensor System and Method to Deter Obsessive Compulsive Behavior by generating alerts when a user's hands are held close to their head or face. The system includes a sensor and a triggering device that are both worn by the user. The sensor can be configured to detect when the triggering device closes to within some threshold distance. The system includes at least two magnet-sensing sensors, and is capable of being calibrated in order to eliminate interference due to the Earth's magnetic field. The sensor and triggering device may be contained within common personal items, such as jewelry—including rings, bracelets, hair clips, necklaces and the like. The system and method can generate audible and/or visual alerts whenever one or more triggering devices passes closer to the sensor than the threshold distance. Alerts are in a variety of tones, including simulated cellular telephone ring tones. Data for alert events is downloadable from the sensor device for later review.

Abstract: A removable tip for a light energy handpiece comprises a hollow conduit configured to surround a light guide in the handpiece; a support extension having a length longer than a length of the hollow conduit; and a shielding extension coupled to the support extension at an angle less than 180 degrees and located in front of the hollow conduit. The shielding extension is configured to be inserted behind an eyelid and extend to the fornix, the shielding extension comprised of a thermally insulative material.

Abstract: The present disclosure provides a system able to acquire machine-readable information received from at least one of images received via the camera, process the machine-readable information to determine patient data from the machine-readable information, determine a medical procedure based on the patient data, permit use of at least a first portion of medical equipment coupled to the system, receive user input that indicates at least one planned procedure step, determine if the medical procedure includes the at least one planned procedure step. The present disclosure further includes a method including the above steps. The present disclosure also includes a system for printing machine-readable information on a garment to be worn in a medical procedure and a method of printing machine-readable information on such a garment.

Abstract: A dorsal night splint has dynamic adjustable features that allow the patient to adjust the splint while in use to control the stretching of the plantar fascia and Achilles. A semi-rigid flexible frame is included along with a tightening strap that is anchored to the frame and by which the patient can tension the strap and adjust the structure of the frame to fit the patient's desired therapeutic or prophylactic needs.

Abstract: A suspension liner is adapted to provide an interface between a residual limb and a prosthetic socket. The suspension liner defines an interior surface and an exterior surface forming a liner profile between a closed distal end and an open proximal end. The suspension liner defines a liner body portion formed from an elastomeric material and at least one seal protruding circumferentially about and radially outward a distance from the liner profile, which is defined at areas outside the at least one seal. The at least one seal defines a sealing surface arranged to deflect toward the liner profile and take up a higher pressure when donned on a residual limb and engaged with an interior wall of the prosthetic socket.

Abstract: A handle and lighting system for a tactical shield includes a handle assembly configured to be mounted on the shield. The handle assembly includes a central horizontal handle, a first side handle on one side, and a second side handle on an opposite side. The handle and lighting system also includes a lighting enclosure housing one or more light sources and configured to be mounted on the shield. The handle and lighting system also includes a first switch mounted on the central horizontal handle, a second switch mounted near a top of the first side handle, and a third switch mounted near a top of the second side handle, which are used to activate or deactivate the one or more light sources. The handle and lighting system may also include first and second rotatable cuffs, which are positioned at the lower distal ends of the first and second side handles.

Abstract: An apparatus for supporting an extremity during tissue irrigation and debridement and containing and capturing fluid and tissue debris resulting therefrom includes an extremity-supporting base and barrier shroud. The apparatus can be used to control drainage of fluid and tissue debris during irrigation and debridement. The apparatus supports and encloses a patient extremity, such as an arm or a leg. The base has a length, proximal end (i.e., nearest the patient's body), and distal end (i.e., farthest from the patient's body). The base may comprise an open-cell foam that is non-collapsible to provide a support surface with a fixed length. The shroud has a top portion, bottom portion, and shroud drainage opening. The shroud can be selectively moveable between a first position in which the support surface is unobstructed to facilitate placement of an extremity thereon and a second position in the shroud at least partially encloses the extremity.

Abstract: A hollow cannula (4) including a perforating tip (5) for perforating a perforating site, said perforating tip (5) being provided with an opening (6), said opening (6) defining a peripheral edge (7) that extends around said opening (6) and that includes a distal axial end and a proximal axial end, said distal axial end of said peripheral edge (7) forming the distal axial end (59) of the perforating tip (5), said distal axial end (59) of the perforating tip (5) being arranged on the longitudinal central axis (A) of said cannula (4), said perforating tip (5) having an outer shape that is rounded in the radial direction, and said distal axial end (59) of said perforating tip (5) being of shape that is rounded in the axial direction.

Abstract: Systems and methods according to the principles described here provide a safe, Comfortable, and soft pad which may be used for the care of babies and toddlers. The pad may be used during care and to transfer babies or toddlers from one location to another without waking the child. The pad includes handles which may be actual handles or hole handles to allow a caregiver to securely grasp pad in order to safely transfer the child.

Abstract: A handheld device measures all vital signs and some hemodynamic parameters from the human body and transmits measured information wirelessly to a web-based system, where the information can be analyzed by a clinician to help diagnose a patient. The system utilizes our discovery that bio-impedance signals used to determine vital signs and hemodynamic parameters can be measured over a conduction pathway extending from the patient's wrist to a location on their thoracic cavity, e.g. their chest or navel. The device's form factor can include re-usable electrode materials to reduce costs. Measurements made by the handheld device, which use the belly button as a ‘fiducial’ marker, facilitate consistent, daily measurements, thereby reducing positioning errors that reduce accuracy of standard impedance measurements. In this and other ways, the handheld device provides an effective tool for characterizing patients with chronic diseases, such as heart failure, renal disease, and hypertension.

Abstract: A port for laparoscopic surgery comprises an opening for attachment to a wound protector and a flexible membrane extending therefrom to define an airtight seal around an incision in a patient. A plurality of access points are defined in the membrane, through which laparoscopic trocars and elongate laparoscopic surgical instruments can be inserted.

Abstract: Sole structures for articles of footwear, including athletic footwear, include a sole structure having a relatively soft and lightweight foam midsole component partially covered by at least one more rigid and/or dense cage (protective) component(s) and/or other protective component(s). The sole structures may include a first portion configured to support at least a heel and midfoot area of a wearer's foot, and an exposed outer edge of this first portion may include a billows structure that extends continuously from a medical midfoot or forefoot area of the sole structure to a lateral midfoot or forefoot area. This billows structure may include fewer than five billow outer ridges connected by billow interstitial areas located between adjacent billow outer ridges. Billow thickness at a rear end of the first portion may be larger than the thickness at a front end of the first portion.

Abstract: The oral appliance for appetite suppression is a device that limits the range of motion of the mouth which prevents impulse eating. In one potential embodiment of the disclosure the oral appliance of appetite suppression comprises an upper molar clip, a lower molar clip, and an elastic band.

Abstract: A headphone and method are provided. The headphone includes a headphone housing and a resilient cushion attached to the housing to define a chamber with the housing for enclosing the user's ear. An assembly is disposed in the housing proximate to a distal end and has a plurality of blades moveable between at least one open position and a closed position. In the closed position, the blades define a distal surface of the housing. In the open position, the assembly defines an aperture in the housing. The aperture allows sound communication from outside the housing into the chamber. The headphone is in communication with at least one external device and is programmed to receive a signal from the external device. The assembly to moves between the open position and the closed position based on the signal.