A mobile-platform imaging device uses compression of the target region to generate an image of an object. A tactile sensor has an optical waveguide with a flexible, transparent first layer. Light is directed into the waveguide. Light is scattered out of the first layer when the first layer is deformed. The first layer is deformed by the tactile sensor being pressed against the object. A force sensor detects a force pressing the tactile sensor against the object and outputs corresponding force information. A first communication unit receives the force information from the force sensor. A receptacle holds a mobile device with a second communication unit and an imager that can generate image information using light scattered out of the first layer. The first communication unit communicates with the second communication unit and the mobile device communicates with an external network.

A non-transitory computer readable medium storing data and computer implementable instructions that, when executed by at least one processor, cause the at least one processor to perform operations for generating cross section views of a wound, the operations including receiving 3D information of a wound based on information captured using an image sensor associated with an image plane substantially parallel to the wound; generating a cross section view of the wound by analyzing the 3D information; and providing data configured to cause a presentation of the generated cross section view of the wound.

A color checker device is disclosed. The color checker device includes a substrate configured to be inserted into a model eye and to conform to a surface curvature of the model eye when inserted therein. A color test target is located on the substrate. The color test target comprises a plurality of color sections configured for generating a color characterization profile of a fundus imaging camera configured to capture a color image of a human retina. A method of generating a color characterization profile using the color checker device and a fundus imaging system having the color characterization profile stored thereon are also disclosed.

A process for calibrating a glucose sensor under sterile conditions includes providing separate, sterile, glucose-containing calibration fluids, each having a different glucose concentration, and in turn providing these fluids to a sensing zone containing a sensing probe of a glucose sensor. Each solution is typically, in turn, propelled into the sensing zone, thus flushing out used fluid already present in the sensing zone. The process provides rapid calibration of a glucose sensor in a sterile fashion and is therefore appropriate for point-of-use calibration.

In one aspect, a computer-implemented method includes receiving signals corresponding to wavelengths of light detected by an optical sensor placed in proximity to a patient's body, and for each received signal: separating the signal into an AC signal and a DC signal; separating the AC signal into component signals; analyzing the component signals through a fractional phase transformation to identify a desired component signal and harmonic signals associated with the desired component signal; smoothing the desired component signal, the harmonic signals, and the DC signal; and combining the smoothed desired component signal, the smoothed harmonic signals, and the smoothed DC signal to generate a modulation signal. A modulation ratio signal is generated based on the modulation signals derived from the signals, and a peripheral oxygen saturation (SpO2) of the patient's body is determined based on the modulation ratio signal.

An imaging method of a fluorescent image performs image processing before generating colored-fluorescent images, including steps: respectively imaging the red, green and blue lights of the white light on three monochromatic sensors under the precondition that the software processing speed is not affected; imaging the near infrared fluorescent light on one of the monochromatic sensors; determining whether the sensor used to receive the near infrared fluorescent light receives the fluorescent signal; calculating the light intensity received by the sensor receiving the fluorescent signal and the light intensities received by the other two sensors; automatically adjusting the projection intensity of the white light source and/or the excitation light source according to the difference of the intensities of the two types of light signals, whereby a closed-loop system is formed to simultaneously present the colored-florescent images on a picture with the best contrast.

The present invention relates to a system and a method for calibration between coordinate systems of a 3D camera and a medical imaging apparatus and an application thereof. The calibration system comprises: a calibration tool arranged on a scanning table, wherein the calibration tool is provided with markers and a reference point, the reference point is aligned with a center of the medical imaging apparatus to serve as an origin of the coordinate system of the medical imaging apparatus, and positions of the markers in the coordinate system of the medical imaging apparatus are calculated according to relative positions of the markers with respect to the reference point; a 3D camera for capturing images of the markers and determining positions of the markers in the coordinate system of the 3D camera based on the captured images; and a calculation device for calculating a calibration matrix using the positions of the markers in the coordinate system of the 3D camera and the positions of the markers in the coordinate system of the medical imaging apparatus, and performing calibration between the coordinate system of the 3D camera and the coordinate system of the medical imaging apparatus using the calibration matrix. The method corresponds to the aforementioned system. The present invention further relates to an application of the calibration and a computer-readable storage medium capable of implementing the method and the application.

A method, system, apparatus, and/or device to determine a condition of a user using a wearable device with a miniaturized spectrometer. The method, system, apparatus, and/or device may include: a band configured to extend at least partially around a body part of a user, the body part comprising an internal feature within the body part; a light source embedded in the band, where the light source is configured to emit light into the body part as the user wears the band; a collimator; an optical filter; and an optical sensor, where the collimator, optical sensor, or the optical filter are arranged together to form a stack embedded in the band.

An ear thermometer capable of identifying an infrared transmittance of a probe cover is provided and includes an ear thermometer body, a probe, and a plurality of activation elements. The probe is disposed on the ear thermometer body. A closed end of the probe cover is used for infrared transmittance, and the probe cover has different infrared transmittances according to a thickness variation thereof. The activation elements are disposed on the ear thermometer body and configured to detect the infrared transmittance of the probe cover. Each of the activation elements includes an ON state and an OFF state so that the activation elements are arranged to form different sensor combinations, which respectively correspond to different infrared transmittances, and any two of the different sensor combinations have the two corresponding infrared transmittances that are different from one another.

An intra-oral scanning device includes a light source and an optical system, and communicates with a display system. The device has a reduced form factor as compared to prior devices, and it provides for more efficient transmission and capture of images.