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Validated Testing

TheraLight was launched in 2018 with the primary mission to quickly become the leader in the industry; and not just the leader in sales and revenue, but the leader who does business in the medical space the right way. TheraLight prides itself on being the most compliant and efficacious light bed company in the world. Boasting 12,000 square feet of office and warehouse space, TheraLight holds compliance with both ISO and Osha standards and is proudly FDA registered and Health Canada approved. By 2025, TheraLight will be ISO certified, UL listed, and FDA-cleared, and will continue to add patents to our growing IP  portfolio, in addition to the development and collaboration of hundreds of case studies.  

Achieving the above is no easy feat. Each registration and certification take years to complete and must be done under expert and sound leadership while utilizing proper warehouse space and various tools and  systems to maintain compliance, all of which come at a high cost. To obtain and maintain each of the  above, this requires that each product component and specification be rigorously tested for quality and  safety, in addition to product efficacy. Since 2019, TheraLight is proud to declare that we are 3rd party  certified for all component quality and safety and for specification accuracy, being tested multiple times over the years. 

While TheraLight has deliberately chosen to not publicly disclose these testing reports; as the unequivocal leader in the industry, it was time to deliver the truth. We are number #1 for a reason and there is a reason why we have maintained that top spot for years and why we never plan to not be the leader. If you want the truth, come and talk with us. We're here to help set the record straight. 

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Offer the Full Body Photobiomodulation Therapy Experience

 
Contact one of our TheraLight Experts and learn more about adding a TheraLight Full Body Photobiomodulation System to your practice or facility.