The present invention relates to a syringe-injection-type brain signal measurement and stimulation structure, and a syringe injection method therefor, and provides a structure including a high-performance flexible element capable of minimizing a skull opening when inserted into the brain. Particularly, the present invention comprises: a flexible element, which includes a contact part making contact with a surface of a cortex so as to measure a signal generated in the brain or transmit an external stimulus to the brain, a transmitting/receiving part positioned between a skull and a skin, and a connection part for making a connection between the contact part and the transmitting/receiving part; and an integrated circuit connected to the transmitting/receiving part so as to transmit/receive a signal.

An implantable medical device (IMD) includes one or more stimulation engines (SEs) and selectively connectable output switching circuitry for driving a plurality of output nodes associated with a respective plurality of electrodes of the IMD's lead system when implanted in a patient. The output switching circuitry may be configured to facilitate self-test mode (STM) functionality in the IMD (e.g., when it is in a hermetically sealed package) by using a dual mode switch in series with a stimulation engine selection switch with respect to each output node in the output switching circuitry under mode selection control.

Inventions herein include at least mostly optically clear orthodontic braces and feet orthotics (collectively referred to as “appliances”) with backscatter based sensors. These two categories of appliances share a common property requiring that the given appliance must be correctly custom manufactured to fit a patient's own particular geometry and dimensions of their teeth and/or feet in order to perform as intended. Incorporating such appliances with backscatter based sensors enables simple, easy, fast, efficient, and cost effective measurements, in real-time or near real-time, of stresses, forces, structural changes, and/or the like in the given appliance; which in turn can aid in determining if adjustments or re-manufacture of the appliance may be needed or desired; and/or wherein such measurements may aid in evaluating performance of the given appliance. In some embodiments, such measurements may also be taken remotely away from a practitioner; and then communicated to a remotely located practitioner.

A computer implemented method and system are provided for detecting premature ventricular contractions (PVCs) in cardiac activity. The method and system obtain cardiac activity (CA) signals for a series of beats, and, for at least a portion of the series of beats, calculate QRS scores for corresponding QRS complex segments from the CA signals. The method and system calculate a variability metric for QRS scores across the series of beats, calculate a QRS complex template using QRS segments from the series of beats, calculate correlation coefficients between the QRS complex template and the QRS complex segments, compare the variability metric to a variability threshold and the correlation coefficients to a correlation threshold, and designate the CA signals to include a predetermined level of PVC burden based on the determining.

A system is disclosed herein for providing a kinetic assessment and preparation of a prosthetic joint comprising one or more prosthetic components. The system comprises a prosthetic component including sensors and circuitry configured to measure load, position of load on a curved surface, joint stability, range of motion, and impingement. In one embodiment, the system is for a ball and socket joint of a musculoskeletal system. The system further includes a computer having a display configured to graphical display quantitative measurement data to support rapid assimilation of the information. The kinetic assessment measures joint alignment under loading that will be similar to that of a final joint installation. The kinetic assessment can use trial or permanent prosthetic components. Furthermore, adjustments can be made to the applied load magnitude, position of load, and joint alignment by various means to fine-tune an installation.

Embodiments herein relate to sensor based authentication between an implantable medical device (IMD) and an external device. In an embodiment, the IMD includes a wireless communication module and an internal inertial measurement unit (IMU) capable of measuring vibrations, movement, or rotation. The IMD is configured to record an internal IMU signal from the internal IMU. The external device includes a wireless communication module and an external IMU. The external device is configured to record an external IMU signal from the external IMU. The system further includes a data processing system to receive a first level communication that can include the internal IMU signal, the external IMU signal, or both, compare data from the internal IMU signal with data from the external IMU signal, and authorize a second level communication based on results of the comparison step.

A biosensor assembly that measures multiple physical parameters is disclosed. The biosensor assembly includes a first implantable probe and a first skin contacting electrode. Wherein a first physiological parameter is measured between the first implantable probe and the first skin contactable electrode.

A bridge device includes a housing, a plurality of electrodes exposed outside of the housing such that at least two of the plurality of electrodes can be concurrently placed in contact with a patient's skin. A controller is disposed within the housing. A first communications module is operably coupled to the controller and to the at least two of the plurality of electrodes. The first communications module is configured to allow the controller to communicate with an implantable medical device via at least two of the plurality of electrodes using conducted communication. A second communications module is operably coupled to the controller and is configured to allow the controller to communicate with a remote device external to the patient.

Disclosed is an antenna device for measuring biometric information by using dark mode excitation. The antenna device according to an embodiment may include a conducting wire forming a loop. A current may be induced into the loop through an interaction with a magnetic field generated by an antenna connected to a power source. Information on an analyte may be sensed using a magnetic field formed based on the current induced into the loop.

A device (1) for measuring, processing and transmitting implant parameters in osteosynthesis, the device (1) comprising: a biocompatible sterilizable housing (2); a strain sensor (3); an electronic unit (4) to process electrical signals provided by the strain sensor (3), wherein the housing (2) comprises (i) a measurement portion (5) of the height H5 comprising a cavity (51); and (ii) a compartment portion (6) of the height H6 with a cavity (61), and wherein the measurement portion (5) comprises at least two affixing means (7) for affixing the device (1) to an implant and wherein the electronic unit (4) is positioned in the cavity of the compartment portion (6).