Aspects of the present disclosure relate to a warming system including a warming device. The warming device includes a clinical garment comprising a body portion adapted to cover a portion of a patient, an inner surface for facing the patient, and an outer surface for facing away from the patient. The body portion includes sleeves sized and positioned for receiving the patient's arms and a torso portion adapted to cover an anterior torso of a patient. A first pneumatic convective device can be disposed adjacent to the inner surface of the clinical garment. The pneumatic convective device can include an opening formed in the clinical garment for admitting a stream of pressurized, warmed air into the first pneumatic convective device. The warming system can also have a second pneumatic convective device in a fully-folded configuration or partially-folded configuration and disposed on a portion of the clinical garment.

Methods are provided herein for affecting a region of a subject's body, comprising exposing the region to a cooling element under conditions effective to cool subcutaneous adipose tissue in said region; and increasing the blood flow rate to the cooled tissue by exposing the tissue to an energy source. Methods are also provided for treating subcutaneous adipose tissue in a region of a subject's body, comprising exposing said region to a cooling element under conditions effective to cool said tissue; and exposing the tissue to an energy source to increase the blood flow rate to the cooled tissue, thereby stimulating reperfusion in, and/or causing an ischemia-reperfusion injury to, the cooled tissue.

Methods are provided herein for affecting a region of a subject's body, comprising exposing the region to a cooling element under conditions effective to cool subcutaneous adipose tissue in said region; and increasing the blood flow rate to the cooled tissue by exposing the tissue to an energy source. Methods are also provided for treating subcutaneous adipose tissue in a region of a subject's body, comprising exposing said region to a cooling element under conditions effective to cool said tissue; and exposing the tissue to an energy source to increase the blood flow rate to the cooled tissue, thereby stimulating reperfusion in, and/or causing an ischemia-reperfusion injury to, the cooled tissue.

Aspects of the present disclosure relate to a warming system. The warming system includes a light device having a light source configured to be positioned proximate to a patient support having a patient support surface. The light source can also be configured to generate infrared radiation. The warming system can also include a flexible sheet having a first side configured to reflect at least some of the generated infrared radiation from the light device toward a portion of the patient support surface.

Methods and systems for providing distributed vibration therapy. The vibration device includes a plurality of vibration motors that are located along a grid. The vibration motors are embedded on a basal pad. A primary diffuser overlays the embedded the vibration motors. The device is portable and can be adaptable to a target body part.

Methods and systems for providing distributed vibration therapy. The vibration device includes a plurality of vibration motors that are located along a grid. The vibration motors are embedded on a basal pad. A primary diffuser overlays the embedded the vibration motors. The device is portable and can be adaptable to a target body part.

A cryolipolysis device is provided. The cryolipolysis device includes a suction unit including a flange configured to press against a treatment area of a user, and a chamber contiguous with the flange that defines a cavity configured to receive an ice pack. The cryolipolysis device also includes a manual vacuum device configured to produce suction within the chamber of the suction unit to generate a vacuum to maintain the flange against the treatment area of the user.

A cryolipolysis device is provided. The cryolipolysis device includes a suction unit including a flange configured to press against a treatment area of a user, and a chamber contiguous with the flange that defines a cavity configured to receive an ice pack. The cryolipolysis device also includes a manual vacuum device configured to produce suction within the chamber of the suction unit to generate a vacuum to maintain the flange against the treatment area of the user.

An applicator has a stem, one or more tips, and one or more chambers which may hold therapeutic or medicinal fluids. The applicator may be separated into two sections so the tips can be used independently. The fluids held in the chambers may be separated with one or more frangible walls which can be broken to release or mix the fluids. The tips are used as applicators for the therapeutic or medicinal effects produced by the fluids or the medicines contained in the cavity.

An applicator has a stem, one or more tips, and one or more chambers which may hold therapeutic or medicinal fluids. The applicator may be separated into two sections so the tips can be used independently. The fluids held in the chambers may be separated with one or more frangible walls which can be broken to release or mix the fluids. The tips are used as applicators for the therapeutic or medicinal effects produced by the fluids or the medicines contained in the cavity.