A handcuff for the treatment of the carpal tunnel syndrome of a hand, the handcuff comprising a base body including a dorsal section and a palmar section. The dorsal section is adapted to exert a pressure on the dorsal side of the hand at at least one location, the palmar section is arranged to exert a pressure on the palmar side of the hand on both sides of the carpal tunnel respectively at at least one location on both sides of the carpal tunnel, and the dorsal section and the palmar section are arranged to widen the carpal tunnel of the hand by the exertion of pressure. In embodiments, the base body has, between the dorsal section and the palmar section, two substantially opposite open slots, between the dorsal section and the palmar section, and the slots are adapted to receive the thumb of the left or the right hand.

A dynamic support apparatus having a frame, a dynamic interface, a temperature control mechanism, and a control system. The dynamic interface is capable of changing its geometry and is disposed on the top surface of the frame. The control system is operably connected to the dynamic interface and controls the changing geometry of the dynamic interface. There is also a temperature control mechanism disposed on the top surface of the frame for maintaining a comfortable temperature and moisture environment between the apparatus and the user's body.

A compression device for the foot including a wrap adapted to surround the foot, the wrap including at least two bladders which when inflated conform to the shape of the foot to provide compression, the bladders being positioned on the wrap so that a first bladder focuses compression on the heel of the foot and a second bladder focuses compression on the arch of the foot; a channel attached to each bladder for independently delivering fluid to each bladder; and a controller attached to the channels that generates and independently controls the flow of fluid to the bladders.

A control unit system. The system includes a control unit which includes a control unit charging interface, at least one magnet located proximate to the control unit charging interface, at least one actuator, a detachable manifold including at least one magnet, fluidly coupled to the at least one actuator, a pump connected to the at least one actuator for causing actuation thereof, and a control system for controlling the pump, wherein the control system controls the pump to actuate the at least one actuator at least in response to a signal received by the control system. The system also includes a recharging device configured to receive the control unit, the recharging device including a reed switch, wherein when the magnet in the control unit is located proximate to the reed switch, the switch is activated.

A blood flow stimulating device comprising: a boot (101) comprising a sole (111) and an upper; a sock (11) disposed within the boot (101): and a bladder (19) disposed within or on the sock (11), wherein the bladder (19) is configured to undergo repeated inflation and deflation so as to stimulate blood flow in a wearer of the blood flow stimulating device, wherein the sock (11) further comprises a toe region (1002), a heel region (1001) and a raised portion (1003) between the toe region (1002) and the heel region that (1001), in use, reduces the distance between the sock (11) and a foot of a wearer of the blood flow stimulating device at the raised portion of the sock.

A device for monitoring a treatment of posture of body parts in which a local mechanotherapeutic stimulus is applied includes an elastic material which is to be worn over the part of the body, a pressure regulating support, a pressure applicator and a pressure sensor. The support is fixed to the elastic material and passes over a region where mechanotherapeutic stimulus is to be applied. The sensor is rigidly attached to the pressure applicator and they are together received in a pocket. The sensor senses pressure and hence a stimulus applied to the part as a result of the tension in the support, the sensor being configured to output a signal indicative of the pressure applied, providing the opportunity to change the stimulus to within a given range based on the feedback from the sensor. A method for using the device is also disclosed.

An orthopedic system includes a base shell forming an opening over a dorsal aspect thereof and a dorsal shell contoured to generally correspond to the opening of the base shell. The base shell has a proximal member and a distal member connected to the proximal member, each has a semi-rigid shell configuration to protect and support a lower leg, an ankle, or a foot of a user when received in the orthopedic system. A flexible toe portion is attached to a distal terminal end area of the distal member and formed of a different material than the distal member. The flexible toe portion is arranged to terminate above an upper surface of the user's toes and to flex relative to the distal member and the toes so as to reduce the likelihood of pressure points on the toes from the distal member.

Determining whether a compression garment is worn by a wearer of the garment by analyzing a pressure signal waveform indicative of a fluid pressure in an inflatable and deflatable bladder of the compression garment. Variance detected in the pressure signal waveform during the analysis is indicative of a change in condition of the compression garment. In one aspect the change in condition is verified using confirmatory analysis. In another aspect, the variance is one of a pressure rise and a pressure impulse. In yet another aspect, the variance is an oscillating amplitude as a function of time representative of a pulse of the wearer.

A blood flow stimulating device including a boot including a sole and an upper; a sock disposed within the boot; and a bladder disposed within or on the sock, wherein the bladder is configured to undergo repeated inflation and deflation so as to stimulate blood flow in a wearer of the blood flow stimulating device, wherein the sock further includes a toe region, a heel region and a raised portion between the toe region and the heel region that, in use, reduces the distance between the sock and a foot of a wearer of the blood flow stimulating device at the raised portion of the sock.

A cushion therapy device including a body, wherein the body has a channel formed therein. The cushion therapy device has a lower member and an upper member, each connected with the body. The cushion therapy device can have additional attachments and sensors for therapeutic relief.