A foot wrap (10) has a generally non-stretchable, flexible binding (11), a generally stretchable panel (12) coupled to the binding, an expandable, rotatable bladder (14), and a support pad (16) coupled to the binding opposite the bladder (14). The binding has a central portion (19) straddled by a first wing (21), a second wing (22), and an elastic heel band (23). The bladder measures approximately 3 inches by 3 inches and is designed to increase in height approximately 1½ to 1¾ inches with its inflation.

A therapeutic device for treating one or more conditions associated with a user's nasal cavities, sinuses, and/or ear canals includes a housing having an opening, an acoustic vibrator within the housing that is operable to provide an acoustic vibration to the user, a fan within the housing that is operable to provide a pressure to the user and a power supply that provides power to the acoustic vibrator and the fan. A mask is connected to the housing at the opening and includes a nasal interface appliable around the nose of the user, a nasal chamber in which the user's nostrils are located and an aperture through which the fan delivers the pressure.

According to some embodiments, a method of promoting hair growth or hair stimulation in a subject comprises applying vacuum or suction using a handpiece assembly along a targeted portion of the subject's skin surface where hair growth or hair stimulation is desired and providing at least one treatment material to said targeted portion of the subject's skin surface, wherein the application of vacuum or suction helps promote hair growth or stimulate hair.

Described here are devices, systems, and methods for treating one or more conditions (such as dry eye) or improving ocular health by providing stimulation to nasal or sinus tissue. Generally, the devices may be handheld or implantable. In some variations, the handheld devices may have a stimulator body and a stimulator probe having one or more nasal insertion prongs. When the devices and systems are used to treat dry eye, nasal or sinus tissue may be stimulated to increase tear production, reduce the symptoms of dry eye, and/or improve ocular surface health.

A vacuum-driven adapter for sexual stimulation includes a primary conduit extending from a base to a crown. The crown is tapered such that when it is inserted into a hose of a running vacuum, it is partially sucked into the vacuum hose to secure the conduit to the hose via a suction fit. At the base is an opening sized to longitudinally receive a male member therethrough. Air flowing into the primary conduit on its way to the vacuum hose vibrates the male member like a reed of a wind instrument. An aperture near the crown is plugged by the user to maintain suction during use; unplugging the aperture may break the seal of the suction fit. Tuning apertures direct air to the male member and can be plugged and unplugged to manipulate air flow and stimulation. Secondary and tertiary conduits nest in the primary conduit to provide sizing options.

A therapeutic massage system is provided. The system is characterized by a controllable compressed air delivery system and a cushion adapted for operative union with a portion of the air delivery system. The cushion includes a support pad and a therapy pad, the support pad having head and vertebral column supporting portions. The support pad vertebral column supporting portion is characterized by longitudinally extending compartments containing filler material. A central compartment of compartments of the support vertebral column supporting portion having a primary region traversing an axial centerline of said cushion and secondary regions spaced apart from said primary central region. The therapy pad overlays and is affixed to the vertebral column supporting portion of the support pad, the therapy pad including a plurality of fluid fillable channels for receiving a vertebral column wherein select fluid fillable channels of the plurality of fluid fillable channels of the therapy pad are fillable via programmed actuation of an actuatable element of the air delivery system. Filler material of the compartments of the support vertebral column supporting portion are responsive to receipt of body weight upon the cushion and select filling of the plurality of fluid fillable channels of the therapy pad, filler material of the regions of the central compartment being passable throughout segments of same in response to receipt of body weight upon the cushion and select filling of the plurality of fluid fillable channels of the therapy pad.

A method of treating meibomian gland dysfunction is disclosed. The method includes directing RF energy to an internal portion of a meibomian gland, selectively targeting an obstruction within a duct of the meibomian gland with the applied RF energy to melt, loosen, or soften the obstruction, and expressing the obstruction from the duct of the meibomian gland. An apparatus for treating meibomian gland dysfunction is also disclosed. The apparatus comprises at least one RF electrode configured to direct RF energy to an internal portion of a meibomian gland located in an eyelid of an eye, the at least one RF electrode further configured to selectively target an obstruction within a duct of the meibomian gland with the applied RF energy to melt, loosen, or soften the obstruction. The apparatus also comprises at least one expressor configured to express the obstruction from the duct of the meibomian gland.

A therapeutic wrap includes a flexible member configured to wrap around an affected area. Actuators are operably coupled to the flexible member. Each actuator is operable between a deployed state and a non-deployed state. A first coupling feature is disposed proximate a first edge on a first surface of the flexible member. A second coupling feature is disposed proximate a second edge on a second surface of the flexible member. The first coupling feature is configured to engage the second coupling feature when the flexible member is wrapped around the affected area and when the flexible member is slidably adjusted relative to the affected area. A retaining feature is coupled to at least one end of the flexible member and configured to retain the flexible member in a selected position on the affected area.

A manual ear pump including one or more of a support element configured to releasably engage an external ear canal and having an interior chamber, a resilient element capable of being resiliently deformed coupled to a support element, and an aperture disposed on a support element bottom surface communicating with the external ear canal and interior chamber.

An external ear canal pressure regulation device including a fluid flow generator and an earpiece having a first axial earpiece conduit fluidicly coupled to the fluid flow generator, whereby the earpiece has a compliant earpiece external surface configured to sealably engage an external ear canal as a barrier between an external ear canal pressure and an ambient pressure.