Systems, methods, and devices are provided herein providing electrical muscle stimulation (EMS). In some instances, an EMS device may be provided. The EMS device may be compact, light, and unobtrusive such that it can be used by a person going about his or her daily activities. In some instances, the EMS device may comprise additional sensors for increased functionality and may be capable of interacting with additional devices or platforms to provide a full-fledged EMS device capability.

The present disclosure relates generally to systems, methods, and devices for interpreting neural signals to determine a desired movement of a target, transmitting electrical signals to the target, and dynamically monitoring subsequent neural signals or movement of the target to change the signal being delivered if necessary, so that the desired movement is achieved. In particular, the neural signals are decoded using a feature extractor, decoder(s) and a body state observer to determine the electrical signals that should be sent.

Devices, systems and methods provide forms of asymptomatic diaphragmatic stimulation (ADS) therapy that affect pressures within the intrathoracic cavity, including: 1) dual-pulse ADS therapy, during which a first ADS pulse is delivered during a diastolic phase of a cardiac cycle and a second ADS pulse is delivered during a systolic phase, 2) paired-pulse ADS therapy, during which a first ADS pulse is delivered, closely followed by a second ADS pulse, with the second ADS pulse functioning to extend or enhance a phase of a transient, partial contraction of the diaphragm, and 3) multiple-pulse ADS therapy, during which a stream of ADS pulses is delivered, wherein the time between pulses is based on heart rate. Devices, systems and methods also monitor electromyography (EMG) activity of the diaphragm relative to baseline activity to assess the health of a diaphragm subject to ADS therapy and to adjust ADS therapy parameters or sensing parameters.

A functional electrical stimulation (FES) device includes electrodes arranged to apply functional electrical stimulation to a body part of the user. FES stimulation is performed by: receiving values of a set of user metrics for the user; receiving a target position of the body part represented as values for a set of body part position measurements; determining a user-specific energization pattern for producing the target position based on the received target position and the received values of the set of user metrics for the user; and energizing the electrodes of the FES device in accordance with the determined user-specific energization pattern. The determination may utilize an FES calibration database with records having fields containing: values of the set of user metrics for reference users; energization patterns; and values of the set of body part position metrics for positions assumed by the body part in response to applying the energization patterns.

The disclosure describes a medical lead system that includes a first lead portion and a second lead portion. The first lead portion includes a first elongate body extending along a longitudinal axis from a distal end to a proximal end and defining a coupling recess. The second lead portion includes a second elongate body extending along the longitudinal axis from a distal end to a proximal end and a connector defining a channel configured to receive the proximal end of the first lead portion. The connector includes a coupling member configured to, when the first lead portion is inserted into the channel, mechanically engage the coupling recess to secure the first lead portion to the second lead portion at least in an axial direction relative to the longitudinal axis.

The present invention relates to a stimulation apparatus (10), comprising a magnetic stimulation unit (20), and a processing unit (30). The processing unit is configured to control the magnetic stimulation unit to provide intentional nerve and/or muscle stimuli to a peripheral body part of a patient.

Systems and methods for creating, maintaining, and remotely modifying stimulation settings for a neuromodulation therapy are discussed. An exemplary system includes an implantable stimulator to provide electrostimulation via a lead comprising a plurality of electrodes, and a programming device. The programming device identifies a search space of electrode configurations and parameter values for the lead, and determines, based on a clinical response indicator under a first patient state, at least one base stimulation setting including an optimal electrode configuration and an optimal stimulation parameter value from the identified search space. The system includes a remotely controlled therapy titration device that can modify the base stimulation setting under a second patient state based on an evaluation of a modified clinical response indicator. The modified base stimulation setting may be stored in the memory, or used by the implantable stimulator to deliver electrostimulation.

A system for restoring muscle function to the lumbar spine to treat low back pain is provided. The system may include one or more electrode leads coupled to an implantable pulse generator (IPG) and a tunneler system for subcutaneously implanting a proximal portion of the lead(s). The system may also include a handheld activator configured to transfer a stimulation command to the IPG, and an external programmer configured to transfer programming data to the IPG. The stimulation command directs the programmable controller to stimulate the tissue in accordance with the programming data. The system may include a software-based programming system run on a computer such that the treating physician may program and adjust stimulation parameters.

Apparatus for providing transcutaneous electrical nerve stimulation (TENS) therapy to a user, said apparatus comprising: a stimulation unit for electrically stimulating at least one nerve of the user; a sensing unit for sensing body movement of the user to analyze body movement activity type and activity duration; an application unit for providing mechanical coupling between said sensing unit and the user's body; and a feedback unit for at least one of (i) providing the user with feedback in response to said analysis of said body movement activity type and activity duration of the user, and (ii) modifying the electrical stimulation provided to the user by said stimulation unit in response to said analysis of said body movement activity type and activity duration of the user.

A rejuvenating beauty care tool for skin and body is an apparatus that enables the user to treat different skin and body areas using different therapeutic and cosmetic techniques. The apparatus may include a handle, a first arm, a second arm, a plurality of first rollers, and a plurality of second rollers. The handle enables the user to comfortably operate the apparatus using only one hand. The handle also supports the first arm and the second arm when the first arm and the second arm are pressed against the user's body. The first arm presses the plurality of first rollers against a first target body area. Likewise, the second arm presses the plurality of second rollers against a second target body area. Further, both the plurality of first rollers and the plurality of second rollers enable the application of the desired cosmetic or therapeutic treatment onto the target body areas.