A sealing device for a foot therapeutic apparatus includes an airtight sleeve and a sealing member. The airtight sleeve includes a treatment box connecting end and a limb inlet end. The sealing member is fixedly mounted at the limb inlet end. The sealing member includes a tightening band and an annular gas bag located on the outer periphery of the tightening band. The annular gas bag is connected to a gas source. A foot therapeutic apparatus with the sealing device includes a treatment chamber and an electrical chamber. The treatment chamber comprises a treatment box, and the sealing device is arranged on the treatment box. A box opening is arranged at a top of the treatment box, and the treatment box connecting end of the airtight sleeve of the sealing device is hermetically connected to the box opening.

The embodied invention is a hyperbaric chamber that is designed to fit through a narrower dimension, such as a doorway, window, garage, or hallway by utilizing a multi-section design. The preferred embodiment is a split chamber design that allows two or three sections to be moved by caster wheels, either on the legs with casters or on a moving cart. The width of the separate sections is designed to fit through a 34″ doorway, and then are readily bolted together to a desirable length. Additionally, the flanges design that connect the individual vessel parts together are designed to provide the pressure needed at a very low weight.

An apparatus to maintain an environment over an anterior surface of a patient eye can include an enclosure sized and shaped to be seated about the patient eye to form a cavity within the enclosure. The enclosure can be configured to contain a fluid other than ambient air in contact with the patient eye. The apparatus can include a fluid regulator in communication with the enclosure, where the fluid regulator can be configured to regulate the composition of the fluid contained within the enclosure.

Embodiments of the present invention are directed to devices, systems and methods adapted for implementing intermittent displacement of blood to mitigate peripheral nerve neuropathy such as that induced by chemotherapeutic agents (i.e., chemotherapy-induced neuropathy (CIN)) that are administered to a patient. Such devices, systems and methods advantageously provide for precise, uniform and controlled blood flow occluding (and optionally blood displacing) compression along irregular surfaces of an appendage of a patient. Such precise, uniform and controlled blood occluding compression is imparted upon the epidermal and dermis skin layers within the aforementioned areas of a patient’s extremities to decrease the time that free nerve endings located in the epidermal and encapsulated nerve endings located in the dermis skin layers are exposed to nerve damaging chemotherapy chemicals, thereby substantially decreasing CIN caused by prolonged exposure to such chemicals.

The present invention provides an apparatus for producing medical foam for wound care or hair stimulation. The apparatus includes a foam generation unit having a fluid reservoir, a fluid delivery line and a foam generation tip. The apparatus also includes a compressed gas unit having at least one container of compressed gas, a source of electric power, and a gas regulator valve. A supply of wound care or hair stimulating solution is communicably connected to the foam generation tip such that when the apparatus is operated medical foam is produced by the foam generator tip.

A therapeutic device for treating conditions of a user's nasal cavities, sinuses, and/or ear canals includes a housing which the user may hold to apply the therapeutic device to the user, the housing including an inlet that allows air to enter the therapeutic device. An acoustic vibrator located within the housing provides an acoustic vibration to the user, and a power supply located within the housing provides power to the acoustic vibrator. A mask is connected to the housing and includes a nasal interface that is appliable around the nose of the user. A valve of the mask opens to allow the user to breathe through the inlet and closes to prevent the user from exhaling through the inlet. The mask further includes a diaphragm and a nasal cavity in which a user's nostrils are located when the nasal interface is applied to the user.

Embodiments of the present invention are directed to devices, systems and methods adapted for implementing intermittent displacement of blood to mitigate peripheral nerve neuropathy such as that induced by chemotherapeutic agents (i.e., chemotherapy-induced neuropathy (CIN)) that are administered to a patient. Such devices, systems and methods advantageously provide for precise, uniform and controlled blood flow occluding (and optionally blood displacing) compression along irregular surfaces of an appendage of a patient. Such precise, uniform and controlled blood occluding compression is imparted upon the epidermal and dermis skin layers within the aforementioned areas of a patient’s extremities to decrease the time that free nerve endings located in the epidermal and encapsulated nerve endings located in the dermis skin layers are exposed to nerve damaging chemotherapy chemicals, thereby substantially decreasing CIN caused by prolonged exposure to such chemicals.

A sealing device for a foot therapeutic apparatus includes an airtight sleeve and a sealing member. The airtight sleeve includes a treatment box connecting end and a limb inlet end. The sealing member is fixedly mounted at the limb inlet end. The sealing member includes a tightening band and an annular gas bag located on the outer periphery of the tightening band. The annular gas bag is connected to a gas source. A foot therapeutic apparatus with the sealing device includes a treatment chamber and an electrical chamber. The treatment chamber comprises a treatment box, and the sealing device is arranged on the treatment box. A box opening is arranged at a top of the treatment box, and the treatment box connecting end of the airtight sleeve of the sealing device is hermetically connected to the box opening.

Formulations of human amniotic fluid and methods of use thereof for treatment of chronic lung disorders have been developed. The formulations are suitable for topical delivery to the lung, for treatment of lung disorders including chronic obstructive pulmonary disorders (COPD), asthma, emphysema, bronchiectasis, chronic bronchitis, interstitial lung disease, alpha-I antitrypsin emphysema. Methods including administering specifically formulated, diluted sterile decellularized human amniotic fluids topically to the lungs, preferably as aerosol droplets, are described. In particular the methods involving administration of the amniotic fluid formulation in the form of aerosol droplets with size between about 1.5 μm to about 5 μm, preferably from about 2.5 μm to about 3.5 μm, inclusive, using apparatus such as high-efficiency vibrating mesh nebulizers, are described. Formulations described can treat, or prevent one or more symptoms of a chronic lung disorder

An apparatus to maintain an environment over an anterior surface of a patient eye can include an enclosure sized and shaped to be seated about the patient eye to form a cavity within the enclosure. The enclosure can be configured to contain a fluid other than ambient air in contact with the patient eye. The apparatus can include a fluid regulator in communication with the enclosure, where the fluid regulator can be configured to regulate the composition of the fluid contained within the enclosure.