A cosmetic method for treating a human body to reduce hyperhidrosis includes applying laser light energy to one or more portions of the human body in which the laser light energy is one or more of: about 450 nm, about 930 nm, about 970 nm and about 1060 nm. An apparatus for accomplishing this method includes a source of laser light energy and a controller for controlling the laser light source to apply laser light energy to target and disrupt sweat glands in the human body.

In one aspect, the present invention relates to a wound care system. The wound care system includes a power unit and a processor coupled to the power unit. An ultra-violet light-emitting diode array is electrically coupled to the processor. A thermoelectric element is thermally exposed to the ultra-violet light-emitting diode array. A probe is optically coupled to the ultra-violet light-emitting diode array. The thermoelectric element cools the ultra-violet light emitting diode array thereby optimizing the ultra-violet light emitting diode array.

The photo therapy apparatus of the present invention comprises one or more light sources which are integrated with a breast pump for providing photo therapy treatment to the breast and nipple of women during pumping of breast milk. The light sources can be lasers, light emitting diodes (LEDs), lamps, or any other types of light sources which produce therapeutic light in a desired wavelength range. The therapeutic light is delivered through the breast-shield or flange of the breast pump to the breast and nipple and produces a variety of photochemical processes, e.g. increase of ATP (adenosine triphosphate), triggering of photo neurological response and activation of enzymes, changes in local pressure, increases in temperature, and deformation of cellular membranes. Such photochemical reaction helps to reduce pain and promote healing of nipple lesion and in the meantime enhance yield of breast milk.

A system and method enables delivery of an implantable medical lead to an implant location. A delivery tool of the system defines the delivery angle of the lead at the implant location. The delivery tool includes an elongate body having at least one lumen extending from a distal portion to a proximal portion. A suction cup is coupled to the distal portion of the elongate body. The suction cup may be configured to be collapsible in a first configuration, prior to deployment, and expandable in a second configuration. The system may include a suction source for drawing tissue at the implant location into the suction cup of the delivery tool that is disposed at the distal portion. The delivery angle of the lead tip is based on the interior cavity of the suction cup rather than the angle of insertion with the suctioned tissue.

Apparatus and methods for treating tissue with electromagnetic radiation. A handpiece includes a housing and a baffle that divides an interior space of the housing into first and second channels. The housing further includes a first opening and a second opening coupled in fluid communication with the first opening by the first channel. The apparatus further includes a heat-generating element, such as a source of electromagnetic radiation, disposed at least partially in the first channel and an air-moving device coupled with the first channel. The air-moving device is configured to generate a forced flow of cooling air entering at the first opening and exhausted at the second opening. The cooling air receives heat transferred from the heat-generating element, which cools the heat-generating element, and the heated cooling air is exhausted from the second opening in a direction away from the tissue that is being treated with the electromagnetic radiation.

A system for treatment of a wound area of a patient including a first treatment pad comprising a plurality of Light Emitting Diodes (LEDs) for cleaning and exposing a wound area to ultraviolet light, a second treatment pad comprising removal ports for exposing the wound area to a negative pressure, and a control unit interoperably connected to the first and second treatment pads for providing a negative pressure and the ultraviolet light to the wound area.

Apparatus and methods for treating tissue with electromagnetic radiation. A handpiece includes a housing and a baffle that divides an interior space of the housing into first and second channels. The housing further includes a first opening and a second opening coupled in fluid communication with the first opening by the first channel. The apparatus further includes a heat-generating element, such as a source of electromagnetic radiation, disposed at least partially in the first channel and an air-moving device coupled with the first channel. The air-moving device is configured to generate a forced flow of cooling air entering at the first opening and exhausted at the second opening. The cooling air receives heat transferred from the heat-generating element, which cools the heat-generating element, and the heated cooling air is exhausted from the second opening in a direction away from the tissue that is being treated with the electromagnetic radiation.

A system for treatment of a wound area of a patient including a first treatment pad comprising a plurality of Light Emitting Diodes (LEDs) for cleaning and exposing a wound area to ultraviolet light, a second treatment pad comprising removal ports for exposing the wound area to a negative pressure, and a control unit interoperably connected to the first and second treatment pads for providing a negative pressure and the ultraviolet light to the wound area.

A negative-pressure cup structure includes a negative-pressure cup body and a light therapy module. The negative-pressure cup body has a rim. The light therapy module is received in the negative-pressure cup body and includes a circuit board and multiple light-emitting diodes (LEDs) mounted on the circuit board and irradiating corresponding to the rim. Therefore, the negative-pressure cup structure further has functions of light therapy and skin care.

A combination therapy pad that includes a first layer and a second layer operatively coupled to the first layer. A fiber-optic array is disposed between the first layer and the second layer. A third layer is operatively coupled to the first layer. The third layer includes a vacuum tube in fluid communication with a vacuum source and a therapeutic fluid tube in fluid communication with a therapeutic fluid source. The third layer provides at least one of vacuum therapy and therapeutic fluid treatment to a wound area.