The present invention A massaging apparatus for human breast, said apparatus comprised of: an electrical pump, a bra having: at least two inflatable tubes having two opening at their edges integrated at each side of the bra encircling one breast organ, wherein each inflatable tube is connected by T shape connector, wherein through pipe to the electronic pump and control module for controlling the inflation of the tubes; wherein the tube are inflated simultaneous at both edges creating dual simultaneous pressure at different size of the breast organ.

A rehabilitation training apparatus and a rehabilitation training system are disclosed. The rehabilitation training apparatus includes a powertrain, a pneumatic flexible actuator and a receiving portion. The powertrain is coupled to the pneumatic flexible actuator and configured to rotate upon drive of the pneumatic flexible actuator. The receiving portion is coupled to the powertrain and configured to receive a training portion and be interlocked with rotation of the powertrain.

The present patent document relates to automatic equipment for performing orthopedic and physiotherapeutic procedures for passive motion of the knee joint (patellofemoral and tibiofemoral), incorporating three motion units: knee flexion and extension motion unit; internal and external rotation motion unit of the knee; and a multidirectional patellar mobilization unit (lower-upper and medial-lateral), an external support for multidirectional patellar mobilizer and a control unit. The flexion and extension motion unit is comprised of a mechanical and electronic structure on which the leg rests during use thereof and has at least two supports for supporting the leg located in the back region of the thigh and in the back region of the leg (calf); the internal and external rotation motion unit of the knee is comprised of a structure with a support for the leg and a support for the foot region (sole region) coupled to a knee flexion and extension motion unit; and the multidirectional patellar mobilization unit is comprised of a receptacle on which a retainer and an actuating element are disposed.

Devices, systems, and methods for High Frequency Chest Wall Oscillation therapy can include a therapy garment including a covering garment for dressing on a patient's torso, the covering garment including a bladder pocket defined between inward and outward layers, and a fluid bladder arranged within the bladder pocket. The fluid bladder can define a pressurizable chamber adapted to receive pressurized fluid to provide force of high frequency pressure oscillation to a patient's chest wall. The pressurizable chamber can be formed to define an outer profile shaped to correspond closely with the patient's rib cage profile to reduce transfer of force of high frequency chest oscillation to the patient's torso outside of the patient's rib cage profile.

An adjustable knee ankle foot orthosis for unloading weight from a knee joint afflicted with osteoarthritis, thus reducing pain and improving mobility, comprising: an upper and lower frame connected by an unloading hinge assembly, optionally comprising a sensor and processor allowing for remote or automatic control of brace tension. In embodiments, the brace includes a user mechanism that is capable of adjusting a tensioning element while the brace is being worn. In other embodiments, electronic motors, sensors, and indicators may be included in the brace to improve brace performance and user interaction.

This disclosure relates to device for providing continuous negative abdominal pressure (CNAP) which selectively recruits (inflates) the dorsal (spinal region) collapsed areas of the lung, while enabling the patient to remain in the supine (usual) position. The CNAP device includes a rigid frame configured to have a shape and size to envelop a patient's lower chest and abdominal area while in a supine position with the frame having opposed edges which sit on a surface on which the supine patient is resting. A pressure sensor is mounted to the frame for measuring a pressure inside the chamber and is connected to a display for displaying the pressure inside the chamber. An active pressure controller is connected to the pressure sensor, and a vacuum pump is in flow communication with inside the chamber and connected to the active pressure controller. The device includes a top up pump in flow communication with inside the chamber and connected to the active pressure controller which is programmed to instruct the vacuum pump to provide negative pressure in the chamber to start decompressing the chamber, and to instruct the top up pump to maintain the negative pressure in the chamber.

A Vertical Running Machine called a VARRI—Vertical, Anti-Gravity, Re-habilitation, Recovery, and Impact Resistant. It relates to the field of bio-mechanical technology, human physiological facts, and the relationship of gravity and the functionality of the body in motion. This is a Vertical, Anti-gravity device created for Recovery from injuries, physical therapy Rehabilitation with the functional characteristics of Impact-free conditioning and by providing a non-impact system to improve the conditioning or recovery of the user, the patient or the elderly. The device provides a method of a more rapid and safer recovery from injuries and surgery and also is capable to provide enhanced athletic performance by using a vertical, non-impact system which alleviates the damages on the muscles and skeletal structure of the body from the continuous impact of horizontal running on the ground.

A diverter is provided for use in directing airflow from an input port to selected output ports. The diverter allows for operation without valves, and is able to provide an air signal to selected output ports in a predetermined manner. The diverter having a rotatable member, or swivel valve, directing air signals to the desired output port depending on the rotational position thereof. The diverter is driven by a controlled actuator or motor, to thus control the manner in which air signals are provided to a plurality of output ports in a controlled manner.

Air microfluidics and minifluidics enabled active compression apparel enhances mobility and quality of life for individuals by minimizing risks of injuries, enhancing rehabilitation, and maximizing comfort. Balloon actuators, integrated with a garment, provide active compression and augmenting forces to anatomical portions of the human body. The balloon actuators are actuated by fluidic pressurization hardware. The air microfluidics and minifluidics system miniaturizes fluidic pressurization hardware and makes it wearable, ultra lightweight, and ultra formfitting. The air microfluidics and minifluidics system includes micro and mini channels of various lengths, cross-sectional areas, and functions via principles of equivalent hydraulic resistance allowing for fluidic transportation, passive delay in pressurization of the balloon actuators, and digital soft fluidic actuation where the compression force is based on the number of inflated balloon actuators instead of their pressure.

Methods are disclosed for measuring the size of body parts treated by a compression therapy device. Either the volume or circumference of the body part may be measure. The methods my include evacuating an inflatable compression sleeve to a known pressure, inserting the body part into the compression sleeve, inflating the sleeve to a pre-set condition, and then measuring one or more inflation related parameters. The pre-set conditions may include a predetermined pressure, volume, or size of the inflatable cells comprising the sleeve. The inflation related parameters may include the time to fill the cell to a pre-set pressure, the pressure attained after a pre-set time of inflation, or the measure volume of a cell after a pre-set amount of air is introduced into it. The methods may also include deflating the cells from the known inflation state to a second inflation state and measuring similar parameters.