Embodiments related to a haptic actuator for transmitting heat and/or mechanical vibrations to an adjacent surface are disclosed. The haptic actuator may include a heating membrane, one or more supports, and a body. The one or more supports may extend between the body and the heating membrane to physically separate the heating membrane from the body.

A computer-implemented system may include a treatment device configured to be manipulated by a user while the user is performing a treatment plan, a patient interface comprising an output device configured to present telemedicine information associated with a telemedicine session, and a first computing device configured to: receive treatment data pertaining to the user while the user uses the treatment device to perform the treatment plan; identify at least one aspect of the at least one measurement pertaining to the user associated with a first treatment device mode of the treatment device; determine whether the at least one aspect of the measurement correlates with a secondary condition of the user; and, in response to a determination that the at least one aspect of the at least one measurement is correlated with the at least one secondary condition of the user, generate secondary condition information indicating at least the secondary condition.

Systems and methods for applying enhanced guided active compression decompression cardiopulmonary resuscitation are provided. Exemplary systems include a load cell, a handle, an adhesive pad. The handle and the adhesive pad are configured for magnetic coupling.

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.

Systems and methods for analysis of symmetry between sides of a body. A wearable device includes a body mounting portion structured and arranged to, in use, be mounted to one or more parts of a body of a patient on one side of the body. The wearable device includes at least one sensor configured to output a signal indicative of at least one physiological parameter from a side of the body to which the wearable device is mounted. At least one processor is configured to receive at least one physiological parameter from the wearable device while mounted to a first side of the body, and at least one physiological parameter from the wearable device while mounted to a second side of the body. An indicator of symmetry between the first side and the second side of the body is determined based at least in part on the at least one physiological parameter from the first side of the body and the at least one physiological parameter from the second side of the body.

An apparatus may be configured for providing feedback to caregivers during a code blue scenario when adhered to the chest of a subject undergoing resuscitation by sensing and transmitting information associated with the code blue scenario. Such information may include one or more of vital signs of the subject during resuscitation, information associated with chest movements of the subject during resuscitation, and audio information from an environment of the subject during resuscitation. One or more processors may generate real-time feedback for communication to the caregivers during the code blue scenario based on the sensed and transmitted information.

A computer-implemented system may include a treatment device configured to be manipulated by a user while the user is performing a treatment plan, a patient interface. and a computing device configured to: receive treatment data pertaining to the user who uses the treatment device to perform the treatment plan; identify at least one enhanced component using the treatment data; generate an enhanced environment using the at least one enhanced component and the treatment plan; output at least one aspect of the enhanced environment to at least one of the patient interface and another interface; receive subsequent treatment data pertaining to the user; and selectively modify at least one of the enhanced environment and at least one of the at least one aspect of the treatment plan and any other aspect of the treatment plan using the subsequent treatment data.

Systems and methods for applying enhanced guided active compression decompression cardiopulmonary resuscitation are provided. Exemplary systems include a load cell, a handle, an adhesive pad. The handle and the adhesive pad are configured for magnetic coupling.

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.

A blood flow stimulating device comprising: a boot (101) comprising a sole (111) and an upper; a sock (11) disposed within the boot (101): and a bladder (19) disposed within or on the sock (11), wherein the bladder (19) is configured to undergo repeated inflation and deflation so as to stimulate blood flow in a wearer of the blood flow stimulating device, wherein the sock (11) further comprises a toe region (1002), a heel region (1001) and a raised portion (1003) between the toe region (1002) and the heel region that (1001), in use, reduces the distance between the sock (11) and a foot of a wearer of the blood flow stimulating device at the raised portion of the sock.