An ultrasonic probe includes: a piezoelectric element that is used for transmitting and receiving ultrasonic waves; a signal electrode that is disposed at a rear surface side of the piezoelectric element; and a backing that is disposed at a rear surface side of the signal electrode, wherein the backing has a thermal resistance of 8 K/W or less, and the backing attenuates an ultrasonic wave with the lowest frequency by 10 dB or more, among frequencies at which transmittance and reception sensitivity of the ultrasonic probe is decreased from the maximum value thereof by 20 dB.

An acoustic lens to steer an acoustic beam includes a first structure, a second structure spaced from the first structure, an array of projections disposed between the first and second structures, each projection of the array of projections extending from the first structure toward the second structure to define a respective gap between the projection and the second structure, and an actuator configured to move the first structure, the second structure, or the array of projections for collective adjustment of the respective gaps of the array of projections. Each projection is configured to define one or more respective unit cells, each unit cell having a sub-wavelength size relative to the acoustic beam to establish an effective refractive index profile for the acoustic beam between the first and second structures. The actuator is configured such that the collective adjustment of the respective gaps varies across the array of projections to spatially modify the effective refractive index profile to steer the acoustic beam.

The present invention relates to a method for obtaining elastic properties of a soft solid by means of quasi-omnidirectional transverse waves generated by a focused ultrasound beam, with a helical phase profile that produces an acoustic vortex that generates a transverse wave front, not only in the direction perpendicular to the ultrasound beam but also in the same direction as the ultrasound beam. The invention also allows control of the transverse wave front generated, which facilitates the carrying out of elastography studies at different frequencies and increases the amplitude of the transverse waves produced, thereby improving the signal-to-noise ratio.

The ultrasound probe includes a piezoelectric element including a piezoelectric composition and an electrode that applies a voltage to the piezoelectric composition. The piezoelectric composition has piezoelectric characteristics expressed by any coordinates included in a region formed by a polyhedron having a plurality of predetermined points as vertexes in Cartesian coordinates (k.sub.eff, ε.sub.33.sup.S, E.sub.c) including variables k.sub.eff, ε.sub.33.sup.S and E.sub.c.

A low power ultrasound system for use in sonography applications, including vascular imaging, is disclosed. The low power ultrasound system includes a base unit having an image processor and a display. An ultrasound probe is operably connected to the base unit. The probe includes a head portion including an array of crystal transducers. A plurality of pulser/receiver modules that cause the transducers to emit ultrasonic transmit pulses are also included in the probe. The pulser/receiver modules are further configured to receive analog signals relating to ultrasonic echo receive pulses detected by the transducers. The probe includes a singular low noise amplifier that amplifies the analog signals, and an analog-to-digital converter that converts the analog signals to a digital signal. A wireless interface is included for enabling the digital signal to be wirelessly transmitted from the probe to the image processor of the base unit.

The invention provides a system (1) for determining an identification characteristic of a medical device (3) carrying at least an ultrasound emitter/sensor element (321). The identification characteristic is based on a detection signal from the ultrasound emitter/sensor element (321) upon a drive signal. The system (1) can identify the medical device from a database (211,511) of known medical devices. Furthermore, the system (1) can update the duration and frequency of use of the medical device (3) and it can prohibit further use of the medical device (3) when a predetermined limit of use is exceeded.

A system and method for ultrasound treatment of skin laxity are provided. Systems and methods can include ultrasound imaging of the region of interest for localization of the treatment area, delivering ultrasound energy at a depth and pattern to achieve the desired therapeutic effects, and/or monitoring the treatment area to assess the results and/or provide feedback. In an embodiment, a treatment system and method can be configured for producing arrays of sub-millimeter and larger zones of thermal ablation to treat the epidermal, superficial dermal, mid-dermal or deep dermal components of tissue.

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 probe for ultrasound treatment of skin laxity are provided. Systems and methods can include ultrasound imaging of the region of interest for localization of the treatment area, delivering ultrasound energy at a depth and pattern to achieve the desired therapeutic effects, and/or monitoring the treatment area to assess the results and/or provide feedback. In an embodiment, a treatment system and method can be configured for producing arrays of sub-millimeter and larger zones of thermal ablation to treat the epidermal, superficial dermal, mid-dermal or deep dermal components of tissue.

An advanced radio apparatus includes a set of antennas; analog circuit; digital circuit; medium access control (MAC) controller; and processor operably connected to the set of antennas, the analog circuit, the digital circuit, and the MAC controller. The processor is configured to decompose wideband waveform signals into a time-frequency waveform based on a sequence of sub-band signals; generate a time-frequency radar waveform based on the decomposed wideband waveform signals; map, based on the time-frequency radar waveform, a constant amplitude zero auto-correlation (CAZAC) sequence into orthogonal frequency division multiplexing (OFDM) sub-carriers to generate a first radar signal. A transceiver is connected to the processor and configured to transmit, to a target object via a transmit antenna of the set of antennas, the first radar signal and receive, via a receive antenna of the set of antennas, a second signal that is reflected or backscattered from the target object.