A therapeutic roller system for use in myofascial release. The therapeutic roller system includes a hollow roller and a coupling nodule. The hollow roller presents an outer wall. The hollow roller includes a receptor opening traversing the outer wall. The coupling nodule includes an upper therapeutic segment and a lower locking segment. The lower locking segment is configured to be inserted into the receptor opening in a first orientation. The lower locking segment is configured to be secured within the receptor opening in a second orientation. The therapeutic roller system may further include a non-coupling nodule.

A percussive massage device that includes a housing that defines a housing interior, a battery, a motor positioned in the housing, a switch for activating the motor, and a reciprocating shaft operatively connected to the motor and configured to reciprocate in response to activation of the motor. The reciprocating shaft includes a distal end that defines a reciprocation axis. The housing includes a first side portion and a second side portion that cooperate to define the housing interior and are defined on opposite sides of the reciprocation axis.

A percussive therapy device that includes a housing, an electrical source, a motor positioned in the housing, a switch for activating the motor, a push rod assembly operatively connected to the motor and configured to provide reciprocating motion in response to activation of the motor, and a massage attachment secured to a distal end of the push rod assembly. The reciprocating motion of the push rod assembly has a user-adjustable amplitude.

The present invention provides an apparatus for measurement of a limb circumference, comprising a pull string module, a first measurement module and a second measurement module. The pull string module comprises a surrounding component, wherein the surrounding component comprises an encircling part disposed around a limb of an individual; the first measurement module is disposed at the pull string module and moves alone the longitudinal axis of the limb and meanwhile measures the length of the limb; and the second measurement module measures the length of the encircling part simultaneously when the first measurement module move alone the limb, so as to determine the correlation between the limb length and the limb circumference. The present invention further provides a device including two or more apparatuses of the present invention to measure the limb compliance and to be used in the treatment of lymphedema.

Wearable devices and methods for preventing and treating carpal tunnel syndrome or DeQuervain's syndrome. The wearable device may include a wrist contact portion for receiving a user's forearm, a stretching mechanism configured to apply opposing forces to a first contact portion and a second contact portion to stretch the user's underlying tissue, the first and second contact portions configured to contact the user's forearm, and one or more straps configured to adjust the compressive force being applied to the user's forearm by the first and second contact portions. The first contact portion may be configured to apply a compressive force to the user's forearm at a first location. The second contact portion may be configured to apply a compressive force to the user's forearm at a second location different than the first location.

Some embodiments relate to compositions for active compression devices and related methods. In some embodiments, a composition for an active compression device comprises an electro-active polymer film. In some embodiments, the electro-active polymer film comprises at least one polymer and at least one additive.

Compositions and formulations for use with devices and systems that enable tissue cooling, such as cryotherapy applications, for alteration and reduction of adipose tissue are described. Aspects of the technology are further directed to methods, compositions and devices that provide protection of non-targeted cells (e.g., non-lipid-rich cells) from freeze damage during dermatological and related aesthetic procedures that require sustained exposure to cold temperatures. Further aspects of the technology include systems for enhancing sustained and/or replenishing release of cryoprotectant to a treatment site prior to and during cooling applications.

A system for treating a joint of a patient includes a treatment head including a probe, a force impulse wave sensor, and a pressure sensor. When the probe is pressed against the joint and reaches a predetermined pressure, the pressure sensor causes a release of current such that the probe delivers a mechanical force impulse to the joint. The force impulse wave sensor is configured to sense a frequency of the mechanical force impulse associated with a treatment point of the joint. The treatment head remains in the same target spot during the pre-test, treatment, and post-test. The system is configured to perform the pretest and post-test analysis of the plurality of treatment points to evaluate improvement of the joint after the treatment. The treatment protocol for the treatment point is modified based on the sensed frequency of the mechanical force impulse from the pre-test at the treatment point.

A percussive therapy device includes a housing, an electrical source, a motor positioned in the housing, a switch for activating the motor, a push rod assembly operatively connected to the motor and configured to reciprocate in response to activation of the motor, and at least one of an angular position sensor configured to obtain angular position data of the percussive therapy device and a linear position sensor configured to obtain linear position data of the percussive therapy device. An attachment module is configured to be operably connected with a percussive therapy device and includes a housing, a wireless connection module, and at least one sensor configured to obtain biometric data of the user or obtain information regarding operation of the percussive therapy device.

A percussive therapy system that includes a percussive massage device including a network interface, and an intelligence engine. The intelligence engine is configured to receive manual capture data and real-time tracking data from the percussive massage device, receive remote data from a remote data source, and generate recommendation data comprising a recommended protocol to be performed by the percussive massage device. The recommendation data is generated from demographic, activity, temporal, analytics, and biometric data, received from the manual capture data, the real-time tracking data, and the remote data inputs.