MLS LASER THERAPY
FDA Clearance and Patent Information
FDA Clearance
The quality, efficiency, and safety of MLS devices are cleared by the FDA.
Indications for Use: “The ‘MLS Family’ Diode Laser is intended to provide topical heating for the purpose of elevating tissue temperature for the temporary relief of muscle and joint pain and stiffness, arthritis pain, or muscle spasm, the temporary increase in local blood circulation and/or promoting relaxation of muscle.”
Patent
The MLS impulse and delivery system are fully patented with United States Patent No. US 8,251,982 B2.
Abstract: “The synchronization of two spatially overlapping energy forms having closely positioned emission axes and particular emission modalities can in many cases provide strengthened or even synergistic effects in the alleviation or treatment of multiple of acute and/or chronic conditions (e.g., pain and inflammation) afflicting a given tissue. The laser energy forms are characterized in terms of their power levels, activation times, activation periods, pulse durations, pulse periods, wavelengths, and other identified characteristics.”