A device is described for treating a nasal airway by modifying a property of a nasal tissue of or near a nasal valve of the airway, without using a surgical incision or an implant, to decrease airflow resistance or perceived airflow resistance in the nasal airway. Various embodiments include an elongate shaft, a bipolar radiofrequency delivery member extending from one end of the shaft, and a handle attached to the elongate shaft at an opposite end from the radiofrequency delivery member. The radiofrequency delivery member is sized to be inserted into a nose and configured to at least temporarily deform the nasal tissue and deliver radiofrequency energy. The radiofrequency delivery member includes two rows of protruding electrodes disposed on a tissue contact surface, and the device is configured to deliver radiofrequency energy from one row of electrodes to the other row of electrodes.

Provided are methods for treating fibrosis of tissues or organs in a subject in need thereof comprising the steps of administering a therapeutically effective amount of energy from an energy source to the targeted tissue or organ; and administering a therapeutically effective amount of stem cells to the tissue or organ. Further provided are methods for monitoring fibrosis in the treated tissue or organ after administration of the energy.

A process that provides protective therapy for biological tissues or fluids includes applying a pulsed energy source to a target tissue or a target fluid having a chronic progressive disease or a risk of having a chronic progressive disease to therapeutically or prophylactically treat the target tissue or target fluid. The pulsed energy source has energy parameters selected so as to raise the target tissue or bodily target fluid temperature up to a predetermined temperature for a short period of time to achieve a therapeutic or prophylactic effect, while the average temperature rise of the target tissue or target fluid over a longer period of time is maintained at or below a predetermined level so as not to permanently damage the target tissue or target fluid.

A cap to be placed on a head of a device for treating the skin of a user includes an inner part to be removably attached to the head of the device, an outer part to be placed against the skin of the user and an interior disposed between the inner and outer parts. A product is disposed in the interior for application to the skin of the user and a covering, such as a membrane which is disposed on the outer part or a sterilized pack, is removable before use. An assembly having the device and the cap is also provided.

An apparatus and method for aspirating, irrigating and/or cleansing wounds is provided. The apparatus and method include one or more of the following: simultaneous aspiration and irrigation of the wound, supplying of thermal energy to fluid circulated through the wound; supplying physiologically active agents to the wound; a biodegradable scaffold in contact with the wound bed; and application of stress or flow stress to the wound bed.

A conductive structure of a massage roller includes a working circuit board, a conductive base, a conductive plate, two first conductive parts and two second conductive parts. The working circuit board and the conductive plate are positioned at upper and lower ends of the conductive base respectively. The conductive base is provided with at least a pair of accommodating cavities, and conductors are placed in the accommodating cavities. The two first conductive parts are positioned on the bottom surface of the working circuit board, and the first conductive parts are connected with the working circuit board. The two second conductive parts are positioned on the top surface of the conductive plate, and the second conductive parts are connected with the conductive plate; and the top surfaces of the conductors abut against the two first conductive parts, and the bottom surfaces of the conductors abut against the two second conductive parts.

There can be provided an incubator (11) which relatively readily stores a cassette tray (61) in a cassette tray accommodation space (62) or takes out the cassette tray (61) from the cassette tray accommodation space (62) through one of a plurality of tray loading/unloading ports (63a-63c) even if a doctor or nurse performs an operation in a region including the outside of the cassette tray accommodation space (62) and its vicinity or even if a sophisticated article such as a sophisticated medical apparatus exists in the region including the outside of the cassette tray accommodation space (62) and its vicinity. In this incubator (11), the cassette tray accommodation space (62) includes at least two tray loading/unloading ports (63a-63c) of a front tray loading/unloading port (63a), a rear tray loading/unloading port, a left tray loading/unloading port (63b), and a right tray loading/unloading port (63c).

Apparatus and methods for determining positioning of a energy delivery element include deploying a energy delivery element at a treatment site proximal to a vessel wall; using a multi-region pressure sensing apparatus to sense pressures applied in a plurality of directions about the energy delivery element; and determining an orientation of the energy delivery element based on the pressures measured in the plurality of directions about the energy delivery element.

The present disclosure relates to a method and an apparatus for generating a laser pulse sequence for application to a predetermined target tissue. Means are provided for setting a cumulative fluence F.sub.s of the laser pulse sequence. Means are provided for determining a duration of the laser pulse sequence as a function of the cumulative fluence F.sub.s such that the predetermined target tissue is heated to a final temperature that is within a predetermined range.

In one instance, a recovery system to assist an athlete with recovery is presented that includes a battery-operated, flexible wrap that applies heat and optionally pneumatic pressure while utilizing both conductive and radiant heat in varying proportions according to a desired pattern. Optionally, at least one pneumatic bladder on the flexible wrap applies the pneumatic pressure to the user. The recovery system has a control unit that ramps the temperature applied before leveling at a target temperature. Other systems and devices are presented.