The present disclosure provides a system for active noise cancellation for a subject placed in a scanning bore of a medical imaging apparatus. The system may be directed to perform operations including obtaining a real-time position of each of at least one target portion of a subject; obtaining signals from one or more arrays of noise detection units surrounding the subject; and directing, based on the signals obtained from the one or more arrays of noise detection units, one or more arrays of denoising units to produce a sound to counteract noise at the real-time position of each of the at least one target portion of the subject.

Methods for fabricating flexible/stretchable circuits can include identifying one or more regions of a printed circuit board (PCB) for selectively removing insulation material. The PCB can include one or more electrically conductive structures arranged on an insulation layer. The method can include applying, within each region of the one or more regions, thermal energy via a heat source to a surface of the PCB within the region such that insulation material of the insulation layer is removed from the region while a portion of the insulation layer beneath the one or more electrically conductive structures is maintained. The flexible/stretchable circuit can be laminated on a soft actuator to form a soft robotic device.

For localizing gingival inflammation within a user's mouth the following steps are carried out using an oral care device (10): (i) sequentially emitting (520) light by a plurality of light sources (48) in a first sequential pattern, wherein at least some of the plurality of light sources are configured to emit light of different wavelengths; (ii) sequentially emitting (530) light in a second sequential pattern which is the reverse of the first sequential pattern; (iii) obtaining (540), by a light detector (40), reflectance measurements to generate first reflectance data from light emitted in the first sequential pattern, and to generate second reflectance data from light emitted in the second sequential pattern; (iv) averaging (550), by a controller (30), first reflectance data and second reflectance data for each wavelength to generate averaged reflectance data; and (v) determining (570), using the averaged reflectance data, whether gingiva at the location is inflamed.

In one example, a display unit comprises a display panel that is configured to display digital images. The display unit further comprises an at least partially transparent protective layer that is arranged above the display panel. The display unit further comprises a controller that is communicatively attached onto an upper surface of the display panel. A biometric sensor pattern is integrated in the controller, and the controller is configured to control the biometric sensor pattern.

Disclosed are devices and methods for non-invasively measuring arterial stiffness using pulse wave analysis of photoplethysmogram data. In some implementations, wearable biometric monitoring devices provided herein for measuring arterial stiffness have the ability to automatically and intelligently obtain PPG data under suitable conditions while the user is engaged in activities or exercises. In some implementations, wearable biometric monitoring devices are provided herein with the ability to remove PPG data variance caused by factors unrelated to arterial stiffness. In some implementations, wearable biometric monitoring devices have the ability to perform PWA while accounting for the user's activities, conditions, or status.

A system and method is presented for cuff-less blood pressure measurement in a mobile device. A key aspect of this disclosure is the discovery of a new location for blood pressure measurement at the fingertip of a subject and that reflectance-mode photoplethysmography can be used to help make this measurement. Through experiments in human subjects, it was discovered that it is indeed possible to measure systemic blood pressure by having a subject press the fingertip against a reflectance-mode photo-plethysmography-force sensor unit under visual guidance and then compute blood pressure from the resulting variable-amplitude blood volume oscillations and applied pressure via an oscillometric algorithm.

The present application provides a personal hand-held monitor for the measurement of a subject's blood pressure and, optionally, one or more other vital signs, comprising a housing located on a personal hand-held computing device or a hand-held component of a computing system; a blood flow occlusion means located in the housing; a pressure sensor adapted to provide an electrical signal indicative of the pressure applied; a means for detecting the flow of blood in the body part of the subject when pressure is applied; and means for receiving electrical signals from the pressure sensor and the blood flow detecting means and for transmitting electrical signals indicative of the pressure and blood flow to the processor of the personal hand-held computing device or the computing system, wherein the processor of the personal hand-held computing device or computing system provide at least a measurement of the blood pressure of a subject. The processor is further adapted to carry out a process to measure a diastolic blood pressure value and a systolic blood pressure value.

An arrangement for producing a sample of body fluid from an opening created in a skin surface at a sampling site including a cartridge with a plurality of compartments and a plurality of sampling sites, and a detector assembly. Each sampling site includes a skin-penetration member having a first end configured to pierce the surface of the skin and an inner lumen in communication with the first end, a spring actuator operatively associated with the skin-penetration member, and a needle hub connecting the skin-penetration member and the spring actuator. The needle hub includes a reagent pad and the spring actuator is configured to drive the skin-penetration member to form the wound opening. Each compartment at least partially encloses the skin-penetration member, the spring actuator, and the needle hub of a respective sampling site.

Technologies for determining seating of an orthopaedic implant during an orthopaedic surgical procedure includes an impaction sensor and an impaction analyzer. The impaction sensor produces sensor data, in response to an impaction between an orthopaedic mallet and a surgical tool indicative of an initial impact and a secondary impact of the impaction. The impaction analyzer analyzes the sensor data to determine a temporal length between the initial and secondary impacts and determines whether the orthopaedic implant is sufficiently seated into the bone based on the temporal length,

The present invention relates generally to systems and methods for measuring an analyte in a host. More particularly, the present invention relates to systems and methods for transcutaneous measurement of glucose in a host.