Abstract: An apparatus comprises a body and a conduit. The body comprises an absorbent material. The conduit is in fluid communication with the body. The conduit has a suction opening positioned within the absorbent material. The conduit is operable to draw fluid away from the absorbent material. The apparatus may be positioned within the posterior choana or the nasopharynx of a patient using a deployment instrument. The apparatus may prevent fluids from draining from the nasal cavity into the patient's throat. In some instances, the apparatus is used as a plug during a sinus irrigation procedure to prevent irrigation fluid from traveling down the patient's throat.

Abstract: An apparatus includes a handle assembly, a guide tube, and a wire. The handle assembly includes a body and an actuator. The guide tube extends distally from the handle assembly and includes a distal end. The wire is slidably disposed in the guide tube. The wire has a distal end including a sensor. The sensor is configured to cooperate with a navigation system to generate a map of anatomical structures within a patient. The wire is coupled with the actuator. The actuator is movable relative to the body to move the wire relative to the guide tube.

Abstract: An apparatus includes an outer coil, a navigation coil, and a distal tip member. The outer coil defines an interior region bounded by inner diameter. The navigation coil is positioned distal to the distal end of the outer coil. The navigation coil is configured to generate a signal in response to movement of the navigation coil within an electromagnetic field. The distal tip member is positioned distal to the navigation coil, such that the navigation coil is longitudinally interposed between the distal tip member and the distal end of the outer coil. The apparatus may be used in combination with a navigation system to provide navigation of paranasal sinus cavities and other structures within a patient.

Abstract: An apparatus includes a handle assembly, a guide assembly, and a dilation catheter. The guide assembly extends distally from the handle assembly. The guide assembly includes a malleable guide member and a flexible guide member. The distal end of the flexible guide member is distal to the distal end of the malleable guide member. The flexible guide member is positioned about the malleable guide member and is slidable along the malleable guide member. The dilation catheter is slidably disposed about the flexible guide member.

Abstract: Medical devices, systems and methods that are useable to facilitate transnasal insertion and positioning of guidewires and various other devices and instruments at desired locations within the ear, nose, throat, paranasal sinuses or cranium. Direct viewing of such placements via an endoscope.

Abstract: A guide member system includes a guide member, a light source, and a detector. The guide member comprises at least one illumination fiber. The at least one illumination fiber distally transmits the light projected by the light source from the proximal end of the guide member to the distal end of the guide member. The distal end of the guide member is projects the distally transmitted light. The distal end of the guide member receives light projected from the distal end of the guide member and reflected back toward the distal end of the guide member. The at least one illumination fiber proximally transmits the reflected light from the distal end of the guide member to the proximal end of the guide member. The proximal end of the guide member projects the proximally transmitted light toward the detector. The detector detects the proximally transmitted light.

Abstract: A guidewire comprises an elongate metal core, an inner layer, an optical core, and an outer layer. The metal core is configured to communicate torsional motion from a proximal end of the metal core to the distal end of the metal core. The inner layer extends about the metal core and has a first index of refraction. The optical core is disposed about the inner layer, wherein the optical core is configured to transmit light along the length of the guidewire. The optical core has a second index of refraction, which is greater than the first index of refraction. The outer layer is disposed about the optical core and has a third index of refraction. The third index of refraction is less than the second index of refraction.

Abstract: A system includes an ultrasound measurement probe. The ultrasound measurement probe includes a lower portion. The lower portion includes a delay block, an array of ultrasound transducers coupled to the delay block, and a first circuit board. The first circuit board further includes a first plurality of pins coupled to the array of ultrasound transducers. The ultrasound measurement probe also includes an upper portion removably coupled to the lower portion. The upper portion includes a second circuit board. The second circuit board further includes a second plurality of pins configured to couple with the first plurality of pins when the upper portion is removably coupled to the lower portion.

Abstract: A variable direction of view endoscope is positionable at desired locations within the ear, nose, throat, paranasal sinuses or cranium to accomplish visualization. A method of use includes introducing the variable direction of view endoscope into a nasal cavity with the endoscope adjusted to a first direction of view between about 0 degrees and about 15 degrees relative to a longitudinal axis of the endoscope. A therapeutic device is introduced into the nasal cavity and the endoscope is adjusted to a second direction of view directed toward the sinus opening or passageway. The method also includes advancing the therapeutic device into or through the sinus opening and viewing at least one of the sinus opening or passageway or the therapeutic device using the endoscope adjusted to the second direction of view.

Abstract: An apparatus comprises an absorbent body, a non-permeable feature, and a port feature. The absorbent body comprises a wicking feature. The non-permeable feature is coupled with the absorbent body. The non-permeable feature and at least a portion of the absorbent body are configured to fit in an opening in a paranasal sinus wall. The port feature extends through the absorbent body. The port feature defines a lumen. The wicking feature extends outwardly relative to the port lumen. During installation of the apparatus, the non-permeable feature is positioned in an opening in the paranasal sinus wall. The absorbent body is oriented such that the wicking feature is in contact with mucosal tissue in a sinus cavity defined by the paranasal sinus wall. A proximal portion of the absorbent body is positioned outside the paranasal sinus wall.

Abstract: Fluid communication may be improved for an ethmoid sinus by installing a port or wick in the wall of the ethmoid sinus to provide a fluid passageway across the wall of the ethmoid sinus. Fluid communication for an ethmoid sinus may also be improved by inflating a balloon in a retrobullar space, remodeling the posterior wall of the ethmoid bulla to expand the transition area in the retrobullar space. In addition, a wall defining the retrobullar space may be pierced to provide a passageway for fluid communication.

Abstract: An apparatus comprises a body and a conduit. The body comprises an absorbent material. The conduit is in fluid communication with the body. The conduit has a suction opening positioned within the absorbent material. The conduit is operable to draw fluid away from the absorbent material. The apparatus may be positioned within the posterior choana or the nasopharynx of a patient using a deployment instrument. The apparatus may prevent fluids from draining from the nasal cavity into the patient's throat. In some instances, the apparatus is used as a plug during a sinus irrigation procedure to prevent irrigation fluid from traveling down the patient's throat.

Abstract: An apparatus comprises a body and a conduit. The body comprises an absorbent material. The conduit is in fluid communication with the body. The conduit has a suction opening positioned within the absorbent material. The conduit is operable to draw fluid away from the absorbent material. The apparatus may be positioned within the posterior choana or the nasopharynx of a patient using a deployment instrument. The apparatus may prevent fluids from draining from the nasal cavity into the patient's throat. In some instances, the apparatus is used as a plug during a sinus irrigation procedure to prevent irrigation fluid from traveling down the patient's throat.

Abstract: A dilation catheter comprises a handle, a guidewire, a dilation catheter, a guidewire movement mechanism, and dilation catheter movement actuator. The guidewire movement mechanism is configured to translate to thereby cause translation of the guidewire relative to the handle. The dilation catheter movement mechanism is configured to translate to thereby cause translation of the dilation catheter relative to the handle. The guidewire movement mechanism also includes a rotation mechanism configured to impart rotation upon the guidewire. The rotation mechanism may include features configured to limit the amount that the guidewire may rotate. The rotation mechanism may also include features configured to convert linear movement of an actuator into rotational movement of the guidewire. The dilation catheter may include features configured to provide for side entry of the guidewire into the dilation catheter.

Abstract: An instrument comprises a shaft assembly. The shaft assembly comprises a first shaft member including a distal cutting feature, and a second shaft member. The first shaft member is slidable relative to the second shaft member. At least a distal portion of the shaft assembly is sized to fit through a nostril. The instrument further comprises a body. At least a portion of the shaft assembly extends distally relative to the body. The body comprises a grounding feature sized and positioned to engage one or more external anatomical structures adjacent to the nostril. The instrument further comprises a dampener. The dampener resists advancement of the first shaft member relative to the second shaft member.

Abstract: A guide catheter system for use in treating the sinus cavity or Eustachian tube is described. The system includes a guide catheter that has a proximal end and a distal end and an elongate shaft between the proximal end and the distal end and a guidewire. The guide catheter includes a deflection feature on a distal tip of the distal end for deflecting the guidewire at a predetermined angle.

Abstract: Apparatus, including a guidewire having a distal end, that is configured to be inserted into proximity with a nasal sinus of a patient, the guidewire having a lumen. The apparatus also includes an optic fiber, traversing the lumen, configured to illuminate the distal end, and a coil, wound around the optic fiber and located within the lumen at the distal end, configured to generate a signal in response to a magnetic field interacting with the coil. A processor is configured to receive the signal and to evaluate a location of the distal end in response to the signal.

Abstract: A method is disclosed for clearing effusion from an ear. The method may include applying liquid to an ear canal, which is proximal to a perforated tympanic membrane, which is proximal to a middle ear containing effusion, applying an ear device to seal and pressurize the liquid inside the ear canal, the ear device regulating the amount of pressure inside the ear canal, and inducing a Eustachian tube, which is distal to the middle ear, to open, which causes the fluid to displace the effusion into the Eustachian tube.

Abstract: Devices and methods for dilating the ostia of paranasal sinuses and other passageways within the ear, nose and throat. A mechanical dilator is inserted through a nostril and used to dilate an ostium or a paranasal sinus or other passageway within the ear, nose or throat (e.g., a Eustachian tube or nasolacrimal duct). The mechanical dilator may be an expandable dilators that comprises one or more non-balloon structures with or without an accompanying balloon or a members of varying diameter or cross dimension (e.g., a tapered member) that may be advanced into the ostium or other passageway to cause dilation of that passageway.

Abstract: Medical devices, systems and methods that are useable to facilitate transnasal insertion and positioning of guidewires and various other devices and instruments at desired locations within the ear, nose, throat, paranasal sinuses or cranium. Direct viewing of such placements via an endoscope.