Laser Therapeutics specializes in low level laser therapy ( LLLT ) and related medical devices. Our extensive line of therapy lasers were developed to treat a number of conditions. Our lasers can only be sold for conditions that they have been FDA cleared for such as pain associated with shoulder tendonitis. In all other cases use of the device is restricted by the FDA to investigational use as part of an Institutional Review Board supervised clinical study. Under this program you will be required to work with our medical staff to perform pre-testing of protocols in order to establish the most effective treatment parameters for conditions being studied. You must report the findings to us and participate in an IRB approved investigational study. This pre-testing of protocols can only be performed on patients who have signed the necessary Informed Consent Agreements stating that they are fully aware that low level laser therapy has not been approved for the condition being studied as of yet. Once you are approved for participation in a study, the IRB will send you the appropriate Informed Consent forms. You may not begin study research until you have been approved and received these forms.

Laser Therapeutics specializes in lasers from Europe’s top manufacturers. They were selected because of their product development and support, ongoing research and the advanced technology utilized in their lasers. Low Level Lasers are Prescription Devices and you are responsible for determining that the use of low laser therapy devices falls within your professional scope of practice in your State. Please ascertain this before filing for inclusion in the IRB approved investigational study.  As part of our programs, you must adhere to all IRB and FDA requirements of conducting clinical trials and are prohibited from advertising any claims as to the effectiveness of the treatment.  Low Level Laser Therapy clinical trials for smoke cessation and weight loss are intended for research purposes only. As such, you will be required to report your findings to us on a quarterly basis on the supplied forms. These forms provide for an analysis of dosage, time, setting, and other factors utilized in the treatment. Don't be misled by others making claims of FDA approved devices. The FDA only clears devices for a specific condition and use beyond that is prohibited except under an IRB approved investigational study. Thus if a company claims that their device is approved for Carpal Tunnel Syndrome, that is all the laser can be used for unless you are part of an IRB approved investigational study. Please contact us for details.

LASER THERAPEUTICS, INC. 

101 Waterside Drive, Centerville, MA 02632 USA

 www.laserhealthsystems.com   email: j.foshay@softlasers.com

                  Phone 508-790-9300 Fax 508-790-9323                        Information 1-800-956-5550  Sales 978 335-5366

Laser Therapeutics is  now conducting clinical trials for smoking addiction,  weight loss and  musculoskeletal   conditions. For additional   information to participate in these clinical studies contact Julie Foshay at 978-335-5366  

The Omega XP is FDA Cleared for Pain associated with shoulder tendinitis