A walking assist device has a frame, a pair of right and left arm portions, a pair of right and left grasp portions, wheels including a pair of right and left drive wheels, drive units, a battery, a drive control unit, acting force measurement units that measure acting forces on the grasp portions, and holding units that hold the grasp portions at a predetermined position in the front-rear direction of the arm portions set in advance. The walking assist device travels forward together with a user. The holding units generate a restoring force for returning the grasp portions to the predetermined position. The drive control unit controls the drive units on the basis of acting forces calculated on the basis of detection signals from the acting force measurement units.

A method and system for noninvasive face lifts and deep tissue tightening are disclosed. An exemplary method and treatment system are configured for the imaging, monitoring, and thermal injury to treat the SMAS region. In accordance with an exemplary embodiment, the exemplary method and system are configured for treating the SMAS region by first, imaging of the region of interest for localization of the treatment area and surrounding structures, second, delivery of ultrasound energy at a depth, distribution, timing, and energy level to achieve the desired therapeutic effect, and third to monitor the treatment area before, during, and after therapy to plan and assess the results and/or provide feedback.

This invention relates generally to apparatus and methods for tightening tissue of the female genitalia by heating targeted connective tissue with radiant energy, while cooling the mucosal epithelial surface over the target tissue to protect it from the heat. Embodiments include a handle and treatment tip that has both an energy delivery element and a cooling mechanism. The handle may be a two-handed handle allowing control even while rotating and maneuvering the treatment around the genital opening. The apparatus or system may also include an integrated controller, which may confirm tissue contact without applying RF energy, based only on the temperature of the applicator and the time since the last application of energy from the applicator.

A patient support apparatus includes a frame having a patient support deck. A footboard is removably coupled to the frame. A compression therapy module is located inside the footboard or is mounted to a foot section of the frame. A sleeve port is pneumatically coupled to the compression therapy module and is located on the foot section. The sleeve port is configured for attachment to at least one tube extending from a compression sleeve worn on a limb of a patient. Control circuitry is coupled to the frame and is operable to control functions of the patient support apparatus and to control the compression therapy module. A graphical display screen is coupled to the control circuitry and displays user inputs that are selected to control functions of the patient support apparatus and the compression therapy module.

A wearable haptic navigation system for obscured visibility environments, the wearable haptic navigation system including: a wearable haptic component, in one alternative a body covering suite; and a mapping data collector and processor in communication with the wearable haptic component; wherein the mapping data collector and processor collects data related to a path traversed by a user of the wearable haptic navigation system and generates at least one proprioception suggestion signal to the wearable haptic component providing the user with a suggested safe egress path and/or a suggested safe body position.

A motion assist apparatus having a color change function using electric ink may include a waist frame and a waist belt that are to be worn on a waist of a user, a force transmission frame and a thigh belt that are to be worn on a thigh of the user, an actuator connected to the waist belt and configured to generate power, a drive frame connected to the actuator and configured to transmit the power to the force transmission frame, an input unit configured to detect at least one of exercise information of the user, body information of the user, and clothing information of the user, a color indicator including a first electrode layer disposed on the drive frame, an electronic ink layer disposed on the first electrode layer, and a second electrode layer disposed on the electronic ink layer, a color determiner configured to determine a target color of the color indicator based on information detected by the input unit, and a color controller configured to receive information about the target color from the color determiner and control a voltage applied to the first electrode layer and a voltage applied to the second electrode layer so as to change a color of the electronic ink layer.

A method and a system for treating skin tissue are provided. A heater is configured to modify temperature of the skin tissue, and a muscle stimulator is configured to provide muscle stimulation to a muscle layer located below the skin tissue. A handheld applicator is configured to be placed in vicinity of the skin tissue to deliver the temperature modification from the at least one heater to the skin tissue and the muscle stimulator from the muscle stimulator to the muscle layer located below the skin tissue; a control board is configured and operable to activate the at least one heater and the muscle stimulator according to respective activation pattern, thereby providing one or more treatments to the skin tissue.

A percussive therapy device includes a housing, an electrical source, a motor positioned in the housing, a switch for activating the motor, and a push rod assembly operatively connected to the motor and configured to reciprocate in response to activation of the motor. A massage attachment is removably received on a distal end of the push rod assembly at a first location. The percussive therapy device also includes an attachment module associated with the housing of the percussive therapy device at a second location. The second location is different than the first location. The attachment module is configured to provide an active effect.

Described herein are methods for determining a target musculoskeletal activity cycle (MSKC) to cardiac cycle (CC) timing relationship. The method may include detecting a signal responsive to a cyclically-varying arterial blood flow at a location on a head of a user; providing a recurrent prompt at a frequency of the heart pump cycle using the signal, such that the signal correlates with a magnitude of blood flow adjacent to the location, and the recurrent prompt is provided to guide the user to time performance of a component of a rhythmic musculoskeletal activity with the recurrent prompt; and guiding the user to adjust a timing of the component of the rhythmic musculoskeletal activity to substantially maximize a magnitude of the signal. In some embodiments, the method further includes generating the recurrent prompt by amplifying the sound generated by the blood flow in or in proximity to an ear of the user.

The vibration capsule device includes a movement generation unit, a movement control unit, a wireless communication unit and a power supply. The movement control unit provides instructions to the movement generation unit, which generates movements in configurable frequencies and duty cycles. The power supply unit provides power to the movement generation unit through movement control unit, which also decides work period and rest period for the capsule device. The vibration capsule device further comprises a capsule movement detection unit, which comprises at least one sensor unit and provides information to the wireless communication unit.