Axelgaard Manufacturing Co., Ltd.

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Contact: Don Nelson - VP Sales
Web: http://www.axelgaard.com
E-Mail:
Address: 104 W Elder St, Fallbrook, California 92028-2852, USA
Phone: +1-(760)-728-3430 | Fax: +1-(760)-723-2356 | Map/Directions >>

Profile: Axelgaard Manufacturing Co., Ltd. (AMC) is a manufacturer of neurostimulation electrodes. Our primary brand is our patented PALS® neurostimulation electrodes. Our PALS® platinum electrodes combine a patented stainless steel knit fabric and gel construction. It is designed for all functional electrical stimulation (FES) and transcutaneous electrical neural stimulation (TENS) applications. Our Ultrastim® snap electrodes distribute the current evenly and comfortably eliminating hotspots. These electrodes have a scientifically calculated grid pattern printed on a conductive material that precisely controls and optimizes electrical current over its surface.

The company was founded in 1985, has revenues of USD 10-25 Million, has ~120 employees and is ISO 13485 certified.

FDA Registration Number: 2025066

14 Products/Services (Click for related suppliers)

• Adhesive Gel Electrode

• Cutaneous Electrode (FDA Code: GXY / 882.1320)

A cutaneous electrode is an electrode that is applied directly to a patient's skin either to record physiological signals (e.g., the electroencephalogram) or to apply electrical stimulation.

• Dual Sensor Electrodes

• Electrocardiograph Electrode (FDA Code: DRX / 870.2360)

An electrocardiograph electrode is the electrical conductor which is applied to the surface of the body to transmit the electrical signal at the body surface to a processor that produces an electrocardiogram or vectorcardiogram.

• Iontophoresis Device (FDA Code: EGJ / 890.5525)

An iontophoresis device is a device that is intended to use a direct current to introduce ions of soluble salts or other drugs into the body and induce sweating for use in the diagnosis of cystic fibrosis or for other uses if the labeling of the drug intended for use with the device bears adequate directions for the device's use with that drug. When used in the diagnosis of cystic fibrosis, the sweat is collected and its composition and weight are determined.

• Lumbar Orthosis, Brace (FDA Code: IQE / 890.3490)

A truncal orthosis is a device intended for medical purposes to support or to immobilize fractures, strains, or sprains of the neck or trunk of the body. Examples of truncal orthoses are the following: Abdominal, cervical, cervical-thoracic, lumbar, lumbo-sacral, rib fracture, sacroiliac, and thoracic orthoses and clavicle splints.

• Multi-Snap Electrode

• Muscle Stimulation Electrodes

• Neurostimulation Electrodes

• Pin Connect Electrodes

• Sensing Electrodes

• Sensing Gel

• TENS Electrodes

• Transcutaneous Nerve Stimulator for Pain Relief (FDA Code: GZJ / 882.5890)

A transcutaneous electrical nerve stimulator for pain relief is a device used to apply an electrical current to electrodes on a patient's skin to treat pain.