Disclosed is an activation device. The activation device, which serves as a device coming into contact with an object to activate surrounding materials according to a dielectric barrier discharge principle, includes: a dielectric having a predetermined thickness and formed with an outer surface coming into contact with the object and an inner surface facing the outer surface; and an electrode provided inside the dielectric and having an outer surface facing the inner surface of the dielectric, wherein the outer surface of the electrode includes a contact area that comes into contact with the inner surface of the dielectric, and a non-contact area that does not come into contact with the inner surface of the dielectric.

The invention relates to a device (1) for treating objects, in particular dental prosthetics and/or teeth, comprising a receiving volume (3) for receiving a cleaning fluid (5), a plasma source (7) configured to generate a non-thermal plasma (35), wherein the device (1) is configured for mixing a plasma product with the cleaning fluid (5), whereby an activated cleaning fluid can be generated, and wherein the device (1) is configured for using the activated cleaning fluid on an object, in particular on at least one dental prosthesis and/or at least one tooth.

The invention relates to a device (1) for treating objects, in particular dental prosthetics and/or teeth, comprising a receiving volume (3) for receiving a cleaning fluid (5), a plasma source (7) configured to generate a non-thermal plasma (35), wherein the device (1) is configured for mixing a plasma product with the cleaning fluid (5), whereby an activated cleaning fluid can be generated, and wherein the device (1) is configured for using the activated cleaning fluid on an object, in particular on at least one dental prosthesis and/or at least one tooth.

In a treatment arrangement for treating a surface, with a planar electrode array (2,2′), to which an electrical voltage can be fed, and with a planar shielding layer (1) which is made of an insulating plastic and which ate least partially surrounds the electrode array (2,2′), a reliable and fixed connection between the electrode array (2,2′) and shielding layer (1) is achieved by the fact that electrode array (2,2′) is made of a pourable plastic provided with plastic additives and that, in the region of a boundary layer (22) between electrode array (2,2′) and shielding layer (1), the plastics of the electrode array (2,2′) and of the shielding layer (1) are connected to each other by material bonding.

In a treatment arrangement for treating a surface, with a planar electrode array (2,2′), to which an electrical voltage can be fed, and with a planar shielding layer (1) which is made of an insulating plastic and which ate least partially surrounds the electrode array (2,2′), a reliable and fixed connection between the electrode array (2,2′) and shielding layer (1) is achieved by the fact that electrode array (2,2′) is made of a pourable plastic provided with plastic additives and that, in the region of a boundary layer (22) between electrode array (2,2′) and shielding layer (1), the plastics of the electrode array (2,2′) and of the shielding layer (1) are connected to each other by material bonding.

A pump and a pump controller which uses an algorithm to quickly achieve and maintain a stable plasma field in a surgical site are provided. The algorithm calculates an electrical characteristic value to determine if a suction rate by the pump should be increased or decreased to achieve the stable plasma field. A method of using the pump and the pump controller is also provided.

A pump and a pump controller which uses an algorithm to quickly achieve and maintain a stable plasma field in a surgical site are provided. The algorithm calculates an electrical characteristic value to determine if a suction rate by the pump should be increased or decreased to achieve the stable plasma field. A method of using the pump and the pump controller is also provided.

A method for generating atmospheric pressure cold plasma inside a hand-held unit discharges cold plasma with simultaneously different rf wavelengths and their harmonies. The unit includes an rf tuning network that is powered by a low-voltage power supply connected to a series of high-voltage coils and capacitors. The rf energy signal is transferred to a primary containment chamber and dispersed through an electrode plate network of various sizes and thicknesses to create multiple frequencies. Helium gas is introduced into the first primary containment chamber, where electron separation is initiated. The energized gas flows into a secondary magnetic compression chamber, where a balanced frequency network grid with capacitance creates the final electron separation, which is inverted magnetically and exits through an orifice with a nozzle. The cold plasma thus generated has been shown to be capable of accelerating a healing process in flesh wounds on animal laboratory specimens.

A method for generating atmospheric pressure cold plasma inside a hand-held unit discharges cold plasma with simultaneously different rf wavelengths and their harmonies. The unit includes an rf tuning network that is powered by a low-voltage power supply connected to a series of high-voltage coils and capacitors. The rf energy signal is transferred to a primary containment chamber and dispersed through an electrode plate network of various sizes and thicknesses to create multiple frequencies. Helium gas is introduced into the first primary containment chamber, where electron separation is initiated. The energized gas flows into a secondary magnetic compression chamber, where a balanced frequency network grid with capacitance creates the final electron separation, which is inverted magnetically and exits through an orifice with a nozzle. The cold plasma thus generated has been shown to be capable of accelerating a healing process in flesh wounds on animal laboratory specimens.

A system includes a focus optic configured to converge an electromagnetic radiation (EMR) beam to a focal region located along an optical axis. The system also includes a detector configured to detect a signal radiation emanating from a predetermined location along the optical axis. The system additionally includes a controller configured to adjust a parameter of the EMR beam based in part on the signal radiation detected by the detector. The system also includes a window located a predetermined depth away from the focal region, between the focal region and the focus optic along the optical axis, wherein the window is configured to make contact with a surface of a tissue.