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Multi Radiance

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MR4 LaserStim™

World’s first and only FDA cleared device combining neurological electrical stimulation and laser in a single probe. LaserStim’s TARGET™ technology (Treatment Area Recognition and Guidance Enhanced Technology) provides an interactive neural stimulation by constantly measuring electro-conductivity of treated tissue and enables clinicians to identify areas to treat with the proper amount of laser energy.


The LaserStim™ combination probe can provide simultaneous or independent Laser, light and electrical stimulation applications for superior clinical outcomes.

  • LaserStim™ emitter (25,000mW) Super Pulsed Laser
  • Red LEDs, infrared emitting diodes and static magnetic field
  • Highly targeted treatments
  • Accommodates, Acupuncture-Muscle Tigger Probes
  • Allows for potential insurance reimbursements
  • Compatible with MR4® consoles

The MR4 LaserStim™ is designed for clinicians with patients who suffer with chronic osteoarthritis of the joints, back and neck pain, frozen shoulder, sciatic pain and pain associated with acute injuries. For patients who have artificial knees or hip replacement or other metal implants, LaserStim™ is effective and safe to use. For patients who have artificial knees or hip replacement or other metal implants, LaserStim™ is effective and safe to use. LaserStim’s TARGET™ technology provides an interactive neural stimulation by constantly measuring electro-conductivity of treated tissue. The device can also be used to treat acute pain such as a recent injury, pain following fractured bones, inflammation, post-surgery.

LaserStim™ Package Includes

  • MR4™ Console Unit - 3 Port System
  • LaserStim™ Emitter (25,000mW)
  • 2 Pairs of Laser Goggles
  • Laser Carrying Case
  • Operating Manual & User's Guide DVD
  • Treatment Protocol Manual
  • Industry Best 3-year limited warranty

 


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This website contains information that has not been reviewed or approved by the FDA. Some of the claims and representations of the products contained on this site are cleared by regional regulatory bodies such as CE and Health Canada and may differ from those that are FDA 510K cleared.
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