Abstract: A method is used to manufacture a surgical guidewire that includes an outer coil assembly, a position sensor, a communication wire, an adhesive, a core wire, a hollow tube, and an atraumatic tip. The outer coil assembly has an outer coil that extends distally from a proximal coil retainer to a distal coil retainer. The position sensor is located distally within the outer coil assembly and is configured to be in communication with a processor via the communication wire. The core wire is between an outer coil proximal portion and the hollow tube. A distal end of the hollow tube is bonded to the atraumatic tip. The method includes affixing the atraumatic tip to the distal end of the hollow tube with the adhesive. The adhesive is constructed of instant glue.

Abstract: An apparatus includes a shaft assembly and an end effector, which includes first and second jaws pivotably coupled together. The first jaw includes a first electrode, and the second jaw includes a second electrode. The jaws may be used to clamp a portion of patient tissue and apply a non-therapeutic, or low voltage, radio frequency (RF) signal to the tissue. Based on the measured response of the current and voltage passing through the tissue, the apparatus can determine various characteristics of the clamped tissue, such as whether the tissue comprises body fluids, blood vessels, tendons, intestines, and/or fat. Once it is determined that the clamped tissue is the correct tissue type, the apparatus may then apply a therapeutic RF signal (e.g., a signal capable of sealing or cauterizing the tissue).

Abstract: Some target anatomies within the ear, nose and/or throat of a patient may be difficult to access and treat. To provide a means of treating such target anatomies over time, drug delivery devices that are sized to be positioned within a naturally occurring or man-made anatomical cavity or passageway are preloaded with active agent(s). The drug delivery devices are affixed directly to, or in the vicinity of, a target anatomy. Once affixed, the drug delivery devices are configured to deliver active agent(s) at desired dosage(s) to the target anatomy through controlled elution of the active agent(s) as various structural features of the drug delivery devices are bio-eliminated.

Abstract: A method of distributing data among members of a surgical team may include receiving imaging data, by a modular control tower, from a plurality of imaging devices, receiving device-dependent data, by the modular control tower, from each of a plurality of intelligent surgical instruments, associating, by the modular control tower, a display device with a member of the surgical team, defining, by the modular control tower, a functional role for the member of the surgical team, and displaying, by the modular control tower, a augmented reality display by the display device. The augmented reality display on the display device may include virtual objects based on the imaging data, the device-dependent data, the functional role of the member of the surgical team, and a surgical activity by the member of the surgical team. An interactive surgical system may implement this method.

Abstract: A method for presenting surgical data onto a livestream of a surgical field on a display during a surgical procedure is disclosed. The method includes detecting, by a control module, surgical data, assigning, by the control module, display priority values to the surgical data, determining, by the control module, a display arrangement of the surgical data on the display based on the display priority values, and presenting onto the livestream visual representations of the surgical data in accordance with the display arrangement.

Abstract: Apparatuses, systems, and methods for displaying interactive overlays for multiple users are disclosed herein. In some aspects, a system for displaying interactive overlays for multiple users can include a surgical hub configured to receive a plurality of data streams related to a surgical procedure and a first augmented reality display device communicably coupled to the surgical hub. In one aspect, the first augment reality display device is linked to a first user. In another aspect, the first augmented reality display device displays a first interactive overlay customized for the first user based on at least one of the plurality of data streams.

Abstract: A surgical instrument includes a sheath and an energy catheter. The sheath is configured to be inserted into a nasal cavity of a patient's head. The energy catheter includes a shaft and an end effector. The end effector is configured to selectively expand radially outwardly. The end effector includes an energy member that includes a flexible wire and electrodes disposed along the wire. The energy catheter is selectively translatable relative to the sheath. In a proximal position, the end effector is housed coaxially within the sheath to thereby prevent the end effector from radially expanding. In a distal position, the end effector is exposed from the sheath to thereby permit the end effector to expand for contacting tissue in the nasal cavity of the patient's head. When the end effector is in the expanded state, the end effector has a width and a length greater than the width.

Abstract: An apparatus includes a body, a shaft assembly, and a visualization assembly. The body includes first and second actuators. The shaft assembly extends distally from the body and includes a rigid proximal portion and a steerable distal portion. The steerable distal portion is positioned distally relative to the rigid proximal portion. The first actuator is operable to drive the steerable distal portion to deflect laterally relative to a longitudinal axis defined by the rigid proximal portion. The steerable distal portion is configured to fit within a nasal cavity of a patient. The visualization assembly is disposed within the shaft assembly. The visualization assembly includes a camera. The second actuator is operable to drive longitudinal translation of the visualization assembly relative to the shaft assembly.

Abstract: A surgical instrument includes a sheath and an ablation catheter disposed within the sheath. The sheath is configured to be inserted into a cavity of a patient's head. The ablation catheter extends along a longitudinal axis and includes at least one expandable ablation member configured to selectively radially expand outwardly from a non-expanded state to an expanded state for selectively ablating tissue within the patient's head. The ablation catheter is selectively translatable relative to the sheath between a proximal retracted position and a distal extended position. In the retracted position, the at least one expandable ablation member is housed within the sheath to thereby prevent the at least one expandable ablation member from radially expanding outwardly. In the extended position, the at least one expandable ablation member is exposed from the sheath to thereby permit the at least one expandable ablation member to radially expand outwardly for contacting tissue.

Abstract: An apparatus includes a guide member, a handle assembly, a gripping assembly, and a grip adjustment assembly. The handle assembly extends proximally from the guide member. The handle assembly includes a first engagement feature. The gripping assembly includes a second engagement feature. The gripping assembly is configured to selectively transition between a locked configuration and a movable configuration. In the locked configuration, the first and second engagement features are configured to engage one another to prevent relative movement of the gripping assembly relative to the handle assembly. The grip adjustment assembly includes a cam feature disposed on at least one of the handle assembly or the gripping assembly. In the movable configuration, the cam feature of the grip adjustment assembly is configured to flex the second engagement feature away from the first engagement feature allowing the gripping assembly to move relative to the handle assembly.

Abstract: An apparatus includes a shaft assembly and an electrode assembly at a distal end of the shaft assembly. The electrode assembly includes a first conductive segment extending along a first angular range at the distal end of the shaft assembly. The first conductive segment is operable to apply RF energy to tissue at a first polarity. The electrode assembly further includes a second conductive segment angularly spaced apart from the first conductive segment. The second conductive segment extends along a second angular range at the distal end of the shaft assembly. The second conductive segment is operable to apply RF energy to tissue at a second polarity such that the first and second conductive segments are operable to apply bipolar RF energy to tissue.

Abstract: An apparatus includes a shaft, a balloon, a tip member, and a heating feature. The tip member is distal to the balloon and has a larger outer diameter than the shaft. The heating feature is operable to ablate tissue of the Eustachian tube contacting the balloon in the expanded state. The heating feature may include an illuminating element and a photosensitive coating on the balloon. Alternatively, the heating feature may include a thermal heating element that heats the balloon inflation fluid and thereby heats the wall of the balloon. Another apparatus includes a shaft, a tip member, and an electrode assembly. The electrode assembly includes a plurality of electrodes positioned along the shaft near the distal end, proximal to the tip member. The electrodes are spaced apart from each other along a longitudinal axis and are operable to apply RF energy to tissue to thereby ablate the tissue.

Abstract: An apparatus includes a body, a shaft assembly, and a shaft actuation assembly. The shaft assembly extends distally from the body and defines a longitudinal axis. A portion of the shaft assembly is configured to be inserted into an anatomical passageway associated with an ear, nose, or throat of a patient. The shaft assembly further defines a working passageway that is dimensioned to receive an instrument. An actuator of the body is operable to drive the instrument longitudinally relative to the shaft assembly. The shaft actuation assembly is operatively coupled with a proximal portion of the shaft assembly. Further, the shaft actuation assembly is translatable in a distal direction to extend the shaft assembly distally along the longitudinal axis and is translatable in a proximal direction to retract the shaft assembly proximally along the longitudinal axis.

Abstract: A method is used to manufacture a surgical guidewire that includes an outer coil assembly, a position sensor, a communication wire, an adhesive, a core wire, a hollow tube, and an atraumatic tip. The outer coil assembly has an outer coil that extends distally from a proximal coil retainer to a distal coil retainer. The position sensor is located distally within the outer coil assembly and is configured to be in communication with a processor via the communication wire. The core wire is between an outer coil proximal portion and the hollow tube. A distal end of the hollow tube is bonded to the atraumatic tip. The method includes affixing the atraumatic tip to the distal end of the hollow tube with the adhesive. The adhesive is constructed of instant glue.

Abstract: A method of dilating a target anatomical structure of an ear, a nose, or a throat of a patient includes inserting a distal end of a balloon catheter into the ear, the nose, or the throat. The balloon catheter includes a balloon assembly coaxially disposed along a proximally extending shaft. The balloon assembly includes at least first and second dilation balloons that at least partially overlap one another. The method also includes distally advancing the distal end until the balloon assembly is disposed in the target anatomical structure. The method also includes selectively dilating the target anatomical structure based on a diameter of the target anatomical structure by inflating the first dilation balloon to a first diameter or inflating the second dilation balloon to a second diameter that is greater than the first diameter. The second inflation lumen is not in fluid communication with the first inflation lumen.