The present invention provides a method of inhibiting the growth of proliferating cells, viruses or bacteria in living tissue, the method comprising: applying low to mid-level frequency Alternating Current electromagnetic signals to the living tissue with a transducer comprising a magnetically conductive material passing through a conduction ring energized by an electrical signal to create the low to mid-level frequency AC current electromagnetic signals within the living tissue; wherein the low to mid-level frequency AC current electromagnetic signals have a frequency in the range of about 50 kHz to about 300 kHz and are produced with an AC voltage generator; and circulating fluid in the living tissue provide a secondary coil for the transmission of the low to mid-level frequency AC current electromagnetic signals.

The unit for non-invasive stimulation of visual cortex cells in severe visual impairment comprises the image sensor (1) provided with the video chip (2) connected to the control processor (9) to convert the image signal to signals capable of stimulating the brain, to which the first transmitting sensor (3) for self-stimulation, the second transmitting sensor (4) of the position stabilisation and the receiving sensor (8) of the position stabilisation feedback are connected via the position stabilisation unit (6), wherein these sensors are connected to the carrier (16) of the active/passive sensors (7) via transmitting active/passive sensors (7) of the position stabilisation feedback. The communication module is connected to the control processor (9); this communication module may be interconnected to the mobile unit (15), and the individual elements may be placed within the supporting structure (5).

Disclosed is a high frequency treatment handpiece having roller electrodes. The handpiece includes: a handpiece casing part; and a plurality of roller electrode members rotatably positioned on a lower surface of the handpiece casing part and applying a high frequency by being brought into contact with the skin. The handpiece prevents burning when the continuous rubbing of a treated area is performed during a treatment, allows a practitioner to conveniently perform the treatment, and allows a person being treated to comfortably receive the treatment with minimum pain. Ball electrodes and roller electrodes can be selectively used, and a roller fixed mode, which limits the rotation of the roller electrodes, can also be selectively used, and thus various massage effects can be selectively provided in accordance with the condition of a patient's skin, and the effect of the high frequency treatment can be maximized by means of the various massage effects.

A subcutaneously implantable device includes a housing and an anchoring mechanism attached to the housing that is configured to anchor the device to a muscle, a bone, and/or a first tissue. The device further includes a first prong with a proximal end attached to the housing and a distal end extending away from the housing that is configured to be positioned adjacent to a first blood vessel, and a first electrode on the distal end of the first prong that is configured to be positioned adjacent to the first blood vessel. Circuitry in the housing is in electrical communication with the first electrode that is configured to deliver electrical stimulation using the electrode to create an electric field around the blood vessel.

A subcutaneously implantable device includes a housing and an anchoring mechanism attached to the housing that is configured to anchor the device to a muscle, a bone, and/or a first tissue. The device further includes a first prong with a proximal end attached to the housing and a distal end extending away from the housing that is configured to be positioned adjacent to a first blood vessel, and a first electrode on the distal end of the first prong that is configured to be positioned adjacent to the first blood vessel. Circuitry in the housing is in electrical communication with the first electrode that is configured to deliver electrical stimulation using the electrode to create an electric field around the blood vessel.

This “in vivo” medical treatment/diagnostic invention has the “intended use” of bombarding the family of coronavirus cells (and COVID-19 and variants) with an energy beam at a tuned frequency to cause them to resonant at a turbulent velocity the outer shell shatters causing their destruction. A Treatment Probe is advanced through the mouth into the windpipe, then an energy beam of extremely high frequency electromagnetic waves causes the cells to react by oscillating at a turbulence sufficient to shatter their electrostatic viral fields thus denaturing these viral cells The remaining active cells are attack by the body's immune system. Repeating treatment sessions stimulate the body's immune system to denatures/destroys the family of coronavirus cells.

TABLE-US-00001 Table of Contents number Title page # TITLE  2 PATENT DECLATION  2 CROSS REFERENCE TO RELATED APPLICATIONS  2 FEDERALLY SPONSORED RESEARCH  2 SEQUENCE LISTING, ETC ON CD  2 BACKGROUND OF THE INVENTION  3 NEED FOR THIS INVENTION  3 Description of Related Art  5 DESCRIPTION OF RELATED ART  5 BRIEF SUMMARY OF THE INVENTION  6 Stimulating the immune system  7 BACKGROUND OF THE INVENTION  8 Technological characteristics  8 DETAILED DESCRIPTION OF THE INVENTION  9 Science Elements  9 Energy Transfer Characteristics 10 Description Of The Destructive Mechanism 11 Power and Frequency 12 Maximum Safe Power 13 Safe Radiation Properties 14 Hardware Design 14 EM Generator Elements 15 Diagnostic Mode 16 Treatment Session Description 17 Treatment/Diagnostic Sequencing 18 [031] BRIEF DESCRIPTION OF THE DRAWING 20 FIG. 1. Description 20 FIG. 2. Description 21 FIG. 3. Description 21 FIG. 4. Description 22 GLOSSARY OF TERMS 22-25 ABSTRACT OF THE DISCLOSURE 26 Drawing Document 27-30 Claims Document 31-32

This “in vivo” medical treatment/diagnostic invention has the “intended use” of bombarding the family of coronavirus cells (and COVID-19 and variants) with an energy beam at a tuned frequency to cause them to resonant at a turbulent velocity the outer shell shatters causing their destruction. A Treatment Probe is advanced through the mouth into the windpipe, then an energy beam of extremely high frequency electromagnetic waves causes the cells to react by oscillating at a turbulence sufficient to shatter their electrostatic viral fields thus denaturing these viral cells The remaining active cells are attack by the body's immune system. Repeating treatment sessions stimulate the body's immune system to denatures/destroys the family of coronavirus cells.

TABLE-US-00001 Table of Contents number Title page # TITLE  2 PATENT DECLATION  2 CROSS REFERENCE TO RELATED APPLICATIONS  2 FEDERALLY SPONSORED RESEARCH  2 SEQUENCE LISTING, ETC ON CD  2 BACKGROUND OF THE INVENTION  3 NEED FOR THIS INVENTION  3 Description of Related Art  5 DESCRIPTION OF RELATED ART  5 BRIEF SUMMARY OF THE INVENTION  6 Stimulating the immune system  7 BACKGROUND OF THE INVENTION  8 Technological characteristics  8 DETAILED DESCRIPTION OF THE INVENTION  9 Science Elements  9 Energy Transfer Characteristics 10 Description Of The Destructive Mechanism 11 Power and Frequency 12 Maximum Safe Power 13 Safe Radiation Properties 14 Hardware Design 14 EM Generator Elements 15 Diagnostic Mode 16 Treatment Session Description 17 Treatment/Diagnostic Sequencing 18 [031] BRIEF DESCRIPTION OF THE DRAWING 20 FIG. 1. Description 20 FIG. 2. Description 21 FIG. 3. Description 21 FIG. 4. Description 22 GLOSSARY OF TERMS 22-25 ABSTRACT OF THE DISCLOSURE 26 Drawing Document 27-30 Claims Document 31-32

Methods, apparatuses, systems, and implementations for inductive heating of a foreign metallic implant are disclosed. A foreign metallic implant may be heated via AMF pulses to ensure that the surface of the foreign metallic implant heats in a uniform manner. As the surface temperature of the foreign metallic implant rises, acoustic signatures may be detected by acoustic sensors that may indicate that tissue may be heating to an undesirable level approaching a boiling point. Once these acoustic signatures are detected, the AMF pulses may be shut off for a time period to allow the surface temperature of the implant to cool before applying additional AMF pulses. In this manner, the surface temperature of a foreign metallic implant may be uniformly heated to a temperature adequate to treat bacterial biofilm buildup on the surface of the foreign metallic implant without damaging surrounding tissue. The AMF pulse treatment can be combined with an antibacterial/antimicrobial treatment regimen to reduce the time and/or antibacterial dosage amount needed to remove the biofilm from the metallic implant.

Methods, apparatuses, systems, and implementations for inductive heating of a foreign metallic implant are disclosed. A foreign metallic implant may be heated via AMF pulses to ensure that the surface of the foreign metallic implant heats in a uniform manner. As the surface temperature of the foreign metallic implant rises, acoustic signatures may be detected by acoustic sensors that may indicate that tissue may be heating to an undesirable level approaching a boiling point. Once these acoustic signatures are detected, the AMF pulses may be shut off for a time period to allow the surface temperature of the implant to cool before applying additional AMF pulses. In this manner, the surface temperature of a foreign metallic implant may be uniformly heated to a temperature adequate to treat bacterial biofilm buildup on the surface of the foreign metallic implant without damaging surrounding tissue. The AMF pulse treatment can be combined with an antibacterial/antimicrobial treatment regimen to reduce the time and/or antibacterial dosage amount needed to remove the biofilm from the metallic implant.

A treatment device for providing a magnetic treatment and a radiofrequency treatment to a body area of a patient. The device includes an energy storage device for storing electric energy, a magnetic field generating device, and a switching device to discharge the electrical energy from the energy storage device to the magnetic field generating device, such that a time-varying magnetic field is generated and provides muscle contraction to a muscle in the body area of the patient. The time-varying magnetic field may have a magnetic field density in a range of 0.1 Tesla to 7 Tesla and a repetition rate in a range of 0.1 Hz to 700 Hz. The device may also include a radiofrequency electrode to generate radiofrequency waves to heat a tissue in the body of the patient. A body of the radiofrequency electrode may include a plurality of openings in a range of 5 to 1000 openings.