A system is provided that includes a device configured to treat a body part of a user, the device including, at least one sensor configured to sense a condition of the body part; and a location tracker configured to track a location of the device in space, wherein the system is includes processing circuitry configured to receive information of a specific sensed condition of the body part detected by the at least one sensor during a session, receive, from the location tracker, information of the tracked location of the device during the session, and associate a specific time when the specific sensed condition is detected by the device with a location of the device in space at the specific time.

There is a skin analysis device for attachment to an electronic device of a human user, the electronic device having at least one skin characteristic measurement device, the skin analysis device comprising an enclosure comprising an enclosure body, configured to be removably connected to the electronic device and one or more skin characteristic measurement assisters, connected to the enclosure and configured to assist one or more skin characteristic measurement devices take a skin characteristic sample of a skin characteristic of the human user.

A detection result output method, an electronic device, and a medium are provided. The detection result output method includes: obtaining first image information of a first object, where the first image information includes skin information of the first object; outputting a target detection result in a case that a matching degree between a first image and a target image meets a first preset condition; and outputting a first detection result in a case that the matching degree between the first image and the target image does not meet the first preset condition. The target detection result is a detection result corresponding to the target image, and the first detection result is a detection result corresponding to the first image.

Examples of the present disclosure describe systems and methods for personalized breast imaging. In aspects, a first set of patient attributes may be collected. The first set of patient attributes may relate to, or be used to determine, for example, breast size, breast thickness, and/or three-dimensional (3D) breast shape. The first set of patient attributes may be used to customize image acquisition parameters for the patient. A second set of patient attributes may also be collected. The second set of patient attributes may relate to, or be used to determine, for example, breast elasticity and breast density. The second set of patient attributes may be used to customize breast compression parameters for the patient. The customized image acquisition parameters and breast compression parameters may then be used to perform one or more procedures (e.g., an imaging procedure, a biopsy procedure, etc.) on the patient's breast.

Various techniques pertain to a user interface that includes an instructional display portion comprising one or more textual or graphical instructions pertaining to preparing for a body scan for body care of a client and a scan initiation display portion that includes a scan initiation widget which, when interacted by the client, invokes execution of a scan process and an analysis process for a respective body area of the client. The user interface further includes a scan result display portion including interactable textual or graphical information pertaining to a result of the body scan for the body care and an adjustment display portion having a plurality of adjustment widgets that transform at least a color index or value into a transformed color index or value in a L*a*b* color space or a LCh color space.

A wearable device is provided. The wearable device may include a housing including a light transmission area, a board disposed inside the housing and including a surface directed toward the light transmission area, a first photodetector disposed on the surface of the board and configured to detect light having a wavelength equal to or longer than a first wavelength, a second photodetector disposed on the surface of the board and configured to detect light having a wavelength equal to or longer than a second wavelength longer than the first wavelength, a first light emitter disposed between the first photodetector and the second photodetector and configured to emit light having a third wavelength toward the light transmission area, and a second light emitter disposed between the first light emitter and the second photodetector and configured to emit light having a fourth wavelength shorter than the third wavelength toward the light transmission area.

A skin inspection device for identifying abnormalities; the device comprising: a transparent panel having an inspection area; an array of thermochromic liquid crystal (TLC) formations provided on the transparent panel which are operable to change colour in response to a change of temperature; and one or more image capture devices for capturing a colour image of the TLC formations and an area of skin of a target located in the inspection area; the captured colour image being analysed to identify abnormalities in the area of skin.

An apparatus for estimating bio-information includes: a sensor part configured to obtain contact pressure of a contact surface contacted by an object, and configured to obtain a contact image of the object that contacts the contact surface; and a processor configured to obtain a pulse wave signal of a region of interest based on the contact image, and configured to estimate bio-information based on the obtained pulse wave signal and the contact pressure.

Systems, methods, apparatuses, and medical devices for harmonizing data from a plurality of non-invasive sensors are described. A physiological parameter can be determined by harmonizing data between two or more different types of non-invasive physiological sensors interrogating the same or proximate measurement sites. Data from one or more first non-invasive sensors can be utilized to identify one or more variables that are useful in one or more calculations associated with data from one or more second non-invasive sensors. Data from one or more first non-invasive sensors can be utilized to calibrate one or more second non-invasive sensors. Non-invasive sensors can include, but are not limited to, an optical coherence tomography (OCT) sensor, a bio-impedance sensor, a tissue dielectric constant sensor, a plethysmograph sensor, or a Raman spectrometer.

A method for quantitatively assessing muscle contraction of a facial muscle in a person and determining the ability of a treatment material to reduce contraction of the facial muscle is disclosed. The method can include applying an external electrical stimulus to facial skin sufficient to contract a facial muscle, measuring the contractile activity of the contracted facial muscle by measuring the compound motor action potential (CMAP) of the contracted facial muscle to obtain a first average measurement of contractile activity of the contracted facial muscle, administering the treatment material by topically applying the treatment material to the facial skin, and repeating steps (a) and (b) to obtain a second average measurement of contractile activity of the contracted facial muscle.