A device and method are provided for therapy and treatment of biological tissue such as muscle, tendon, and ligament tissue, by use of a device and method in which therapeutic vibrational frequency resonance patterns are transmitted to tissues of a patient. The resonance frequencies originate from many resonance domains, including vitamins, minerals, herbs, amino acids, and fatty acids. Each domain includes therapeutic frequency resonance patterns. These resonance patterns may be passively excited and transmitted to a patient to enhance tissue function, to decrease the normal rehabilitation time of damaged tissue, and provide therapeutic benefits for muscle tissue dysfunction. Therapeutic frequency resonance patterns may also be actively excited by a delivery mechanism that uses electromagnetic or mechanical waves to interact with the device. The actively excited device transmits the therapeutic frequency resonance patterns to the patients for similar enhancements and therapeutic benefits.

A device and a method for switchable vibration modal ultrasonic are provided. The device includes a hollow shaft, an ultrasonic motor, a limit shell, an electromagnet, a moving tool head, a vibration source and a tool head. The structure design of the ultrasonic motor, the magnetostrictive materials and the drive coil combination of different functions are configured so that, without changing the condition of components, the ultrasonic can switch mode, namely the longitudinal vibration, torsional vibration, and longitudinal and torsional vibration in three different vibration modes. During the operation of the device, different vibration modes are excited without changing the parts, which meets the machining requirements of different vibration forms. Meanwhile, the operation is more convenient and faster, and the overall design structure of the device ensures the efficient and safe operation of the device.

A handheld device for applying mechanical vibration to a body portion of an individual to treat a dry eye condition of the individual, includes: a housing; a member having a first portion accommodated in the housing, and a second portion that is moveable relative to the housing, wherein the second portion is for placement outside the individual, and is configured to oscillate to apply the mechanical vibration to the body portion, the member having an elongated configuration; and a motor in the housing, the motor configured to oscillate the member at an oscillation frequency sufficient to induce tear production when the second portion of the member is applied towards a surface of the body portion.

A handheld device for applying mechanical vibration to a body portion of an individual to treat a dry eye condition of the individual, includes: a housing; a member having a first portion accommodated in the housing, and a second portion that is moveable relative to the housing, wherein the second portion is for placement outside the individual, and is configured to oscillate to apply the mechanical vibration to the body portion; and a motor in the housing, the motor configured to cause the member to undergo bending action in a reciprocating manner to oscillate the second portion of the member at an oscillation frequency sufficient to induce tear production when the second portion of the member is applied towards a surface of the body portion.

A handheld device for applying mechanical vibration to a body portion of an individual to treat a condition of the individual, includes: a housing; a member having a portion that is moveable relative to the housing, wherein the portion of the member is configured to oscillate to apply the mechanical vibration to the body portion, the member having an elongated configuration; and a motor having a weight that is supported by the member.

A method to treat a dry eye condition of an individual, includes: receiving a switch signal generated based on a manipulation of a control switch at a handheld device; and activating a motor in response to the switch signal to oscillate a member at an oscillation frequency, the member having an elongated configuration, and having a portion for placement outside the individual; wherein the oscillation frequency is sufficient to induce tear production when the portion of the member is applied towards a surface of a body portion of the individual.

A rest for a mattress support system and which serves for sensory training of a person, and a method for sensory training of a person. This rest has a multiplicity of actuatable micro-stimulating elements for producing sensory stimuli. These elements are assigned to the rest. Using a control device, the person can actuate the micro-stimulating elements during the training. Moreover, this control device serves to generate a feedback signal in response to the sensory stimuli.

Devices, systems and methods for stimulating (e.g., noninvasively) a subject's inflammatory reflex are provided to reduce bleed time. The method may include the step of non-invasively stimulating the inflammatory reflex (e.g., the vagus nerve, the splenic nerve, the hepatic nerve, the facial nerve, and the trigeminal nerve) of a subject, such as by mechanical stimulation, in a manner which significantly reduces bleed time in the subject. Devices for non-invasively stimulating the inflammatory reflex may include a movable tip or actuator that is controlled to mechanically stimulate the ear. The devices may be hand-held or wearable, and may stimulate the cymba conchae region of the subject's ear.

A wearable sleeve is configured to be worn on a limb of a user. The sleeve includes a flexible tubular sleeve body that is elongate along an axis. The sleeve further includes at least one of a series of vibrating elements and a series of pneumatic compression elements that are attached to the tubular sleeve body. During use, the vibrating elements and/or the compression elements are configured to be disposed along a lymphatic drainage path of the user. Targeted photonic stimulation in the form of light generated by LED or laser may be employed to further enhance the circulatory and physiologic changes. Microprocessor incorporated control and interactive capability further results in optimized application and patient compliance due to improved efficacy.