An endoscopic examination supporting apparatus includes at least one processor including hardware. The processor acquires insertion shape information indicating an insertion shape of an insertion section of an endoscope inserted into a subject, evaluates, based on the insertion shape information, a procedure including inserting operation for the insertion section performed by a user who operates the endoscope during an endoscopic examination, and generates procedure evaluation information.

A medical device control handle or catheter includes deflection assembly and at least one of the following: a disk actuator, a lever actuator and a ring actuator for actuating additional puller wires in manipulation of multiple features of the medical device or catheter independently of each other. The disk actuator has a common rotational axis with but is rotationally independent of the deflection assembly. The lever actuator has a separate rotational axis. The ring is mounted outside of the control handle and rotatable relative to the control handle to actuate another puller wire for manipulating another feature of the catheter. Each of the disk, lever and ring actuators are of a design that allows existing control handles and catheters to be readily modified to include these actuators.

A minimally invasive system comprises an elongate medical instrument including a flexible body. The flexible body includes a wall including a channel, and the channel includes a groove. The flexible body further includes a lumen defined by an interior surface of the wall and a curved distal tip portion. The elongate medical instrument further includes a shape sensor coupled to the flexible body. The shape sensor is at least partially positioned within the groove, and the shape sensor is configured to detect shape characteristics of at least a portion of the flexible body. The system further includes an actuator for manipulating the elongate medical instrument.

A display for outputting information contents of at least one parameter, adjustment value or measurement value of medical devices within at least one display region, wherein the at least one display region is in the form of a tachometer-like display.

A method (500) for localizing gingival inflammation using an oral care device (10), the method comprising: (i) emitting (520) light at a first intensity by a light emitter (42); (ii) obtaining (530) first reflectance measurements reflectance data; (iii) determining (540), by a controller (30) from the first reflectance data, whether the location comprises gingiva; (iv) automatically adjusting (550), based at least in part on the first reflectance data, the intensity of a light emitter to a second intensity different from the first intensity, and/or automatically adjusting (550) a gain of a light detector; (v) obtaining (560) a second plurality of reflectance measurements by the light detector of the oral care device for at least some of the locations; and (vi) determining (570), using the second plurality of reflectance measurements, whether gingiva at the location is inflamed.

A system is provided for determining a risk indicator for myopia. The system comprises a wearable device configured to be attached to a body of a user. The wearable device comprises at least one distance sensor configured to determine at least a first distance value indicative of a distance between the wearable device and an object located in a central vision zone of the user and a second distance value indicative of a distance between the wearable device and an object located in a peripheral vision zone of the user. The system further comprises a control unit configured to determine, based on the first distance value and the second distance value, a risk indicator for myopia. Further, a method and a computer program product are provided.

Systems, devices, and methods for guiding an ablation procedure are provided. For example, in one embodiment, a system for guiding ablation includes a processor circuit in communication an electrophysiology (EP) catheter comprising a plurality of electrodes. The EP catheter is positioned near an ablation balloon during placement at the ablation site, and is used to detect blood flow within a cavity of the heart by detecting electrical signals relating to dielectric properties. It can then be determined whether any gaps are present at the interface between the balloon and the ablation site. For example, the processor circuit can determine, based on the detected blood flow, whether a balloon occludes a region of interest. The processor then outputs a visualization indicating whether the balloon occludes the region of interest to a display.

Assemblies are provided for positioning within a lumen comprising a stent graft; and a sensor positioned on the stent graft. Within certain aspects the sensors are wireless sensors, and include for example one or more fluid pressure sensors, contact sensors, position sensors, pulse pressure sensors, blood volume sensors, blood flow sensors, chemistry sensors (e.g., for blood and/or other fluids), metabolic sensors (e.g., for blood and/or other fluids), mechanical stress sensors and/or temperature sensors.

A medical system includes a medical instrument, at least one actuator, and a controller. The medical instrument defines a central axis and includes a steerable tip. The controller is configured to command the at least one actuator to cause active steering control of the medical instrument according to an insertion control mode after movement of the medical instrument is detected and exceeds a first threshold value in an insertion direction and to deactivate the at least one actuator to cause the steerable tip of the medical instrument to move freely, without the active steering control, in reaction to forces exerted against the medical instrument by a wall of the anatomic passageway after axial movement of the medical instrument is detected by the medical system and exceeds a second threshold value in a retraction direction. At least one of the first or second threshold values comprises a velocity threshold value.

A method of compressing tissue during a surgical procedure is disclosed. The method comprises obtaining a surgical instrument comprising an end effector, wherein the end effector comprises a first jaw and a second jaw, establishing a communication pathway between the surgical instrument and a surgical hub, and inserting the surgical instrument into a surgical site. The method further comprises compressing tissue between the first jaw and the second jaw, determining a location of the compressed tissue with respect to at least one of the first jaw and the second jaw, communicating the determined location of the compressed tissue to the surgical hub, and displaying the determined location of the compressed tissue on a visual feedback device.