A dental treatment apparatus includes a holder, a power supply, root canal length measurement circuitry, and control circuitry. The holder holds an electrode placed in a root canal. The power supply energizes file with a high-frequency current. The root canal length measurement circuitry electrically measures a position of a distal end of electrode in the root canal. The control circuitry causes, in accordance with information on the position of the distal end of the electrode measured by root canal length measurement circuitry, the power supply to control a current value of the high-frequency current which energizes the electrode.

Provided is a method for treating a living body using an electrical stimulator including a base wire having a core wire and an outer winding wire wound around the core wire. An annulus is formed by winding the base wire in a loop shape. A first end of the core wire is electrically connected to a first end of the outer winding wire. A second end of the core wire is connected to a first terminal of an external circuit. A second end of the outer winding wire is connected to a second terminal of the external circuit. The method includes holding the living body or a part of the living body of a subject in the annulus and generating an alternating current in the external circuit for a therapeutically effective time period to apply an electrical stimulation to the living body or the part of the living body.

A therapeutic apparatus for treating damaged tissue on a limb or body of a subject includes a wearable adapted to cover and be secured to the limb or body of a subject over damaged tissue. The wearable being configured to reduce pressure on the damaged tissue and adapted to deliver one or more treatments selected from the group consisting of heat, oxygen, electrical current, and light to the damaged tissue.

Systems and methods are provided for enhancing osseointegration performed in conjunction with placing a dental implant. A dental implant post can be used for applying current to the implant site as well as for anchoring an artificial tooth. Such a dual purpose implant can allow faster healing and osseointegration time as well as enabling the use of dental implants in a large segment of the population currently disqualified from such treatment due to poor bone quality.

An implanted electrode system that can be accessed to perform functions including but not limited to radiofrequency ablation, dorsal horn stimulation, peripheral nerve stimulation and bone stimulation. The implant electrode system generally includes is to have implantable devices that will allow for post-operative percutaneous radiofrequency ablation.

An electrical stimulation anchor is configured to be electrically coupled to a power source, such as a transducer, that is external to the electrical stimulation anchor. The electrical stimulation anchor can include a bone anchor that is configured to be secured to a bone. The bone anchor can define a first electrode, a second electrode, and an isolating portion between the first electrode and the second electrode. The electrical stimulation anchor can further include a connection unit attached to the bone anchor. The connection unit can define a first contact member that electrically connects to the first electrode, and a second contact member electrically isolated from the first contact member. The second contact member can be electrically connected to the second electrode. The first and second contact members are configured to draw electrical current from the transducer so as to establish a voltage differential between the first and second electrodes.

A power supply apparatus includes a power supply configured to apply an alternating current to a magnetic field generation apparatus; and a controller configured to control the alternating current applied by the power supply. The controller controls the power supply to apply the alternating current having a waveform pattern including a plurality of current waveforms having different frequency spectrums from each other.

Apparatuses, systems and methods are provided for treating pulmonary tissues via delivery of energy, generally characterized by high voltage pulses, to target tissue using a pulmonary tissue modification system (e.g., an energy delivery catheter system). Example pulmonary tissues include, without limitation, the epithelium (the goblet cells, ciliated pseudostratified columnar epithelial cells, and basal cells), lamina propria, submucosa, submucosal glands, basement membrane, smooth muscle, cartilage, nerves, pathogens resident near or within the tissue, or a combination of any of these. The system may be used to treat a variety of pulmonary diseases or disorders such as or associated with COPD (e.g., chronic bronchitis, emphysema), asthma, interstitial pulmonary fibrosis, cystic fibrosis, bronchiectasis, primary ciliary dyskinesia (PCD), acute bronchitis and/or other pulmonary diseases or disorders.

Methods of applying microcurrent stimulation to a subject may include providing a mask supplying at a minimum moisture to a region to be treated, applying a first electrode connected to a first polarity of microcurrent stimulation circuitry to the mask, applying a second electrode connected to a second polarity of the microcurrent stimulation circuitry to the subject outside of the mask, and providing microcurrent to the first electrode and the second electrode from the microcurrent stimulation circuitry. The method may further include inserting feet of the subject into a liquid having a minimum conductivity of 5 mS/m and vibrating the liquid.

A method is provided that includes providing an electrode, which includes a wire that has a wire diameter of between 75 and 125 microns. The wire includes a non-electrically-insulated current-application longitudinal segment, which, in the absence of any applied forces, is coiled and has (i) an outer coil diameter of between 3 and 7 times the wire diameter, and (ii) an entire longitudinal length of between 5 and 35 mm. The wire further includes an electrically-insulated lead longitudinal segment, which has an entire longitudinal length of at least 10 mm, in the absence of any applied forces. At least a portion of the electrode is implanted in a body of a subject. Other embodiments are also described.