While people have been suffering for years from discomfort in the neck and shoulder, this may no longer be the case. For, there is a new FDA Approved Laser For Pain in these and other areas of the body. In June of 2018, the United States Food and Drug Administration approved a laser light based product known as a multi radiance medical MR4 laser.
When researchers ran studies on test subjects and placebos, results showed that this new laser light based product was more effective than placebos with regards to eliminating discomfort. As a result, the NHN product also received designation as a NHN non-heat, non-thermal based device.
The product emits monochromatic radiation by using light amplification which is coherent and collimated. The process emits energy through wavelengths of infrared or other sources which provide a non-thermal and non-heated effect. In all cases, the product can be used without the need for associated topical or other forms of heat.
While a number of similar products are for sale in the United States, few have obtained FDA approval or have been designated as NHN which recognizes the product as being non-thermal. As such, while a number of the products may be effective, most are lacking the safety requirements of those approved by the FDA.
In most cases, companies avoid undergoing FDA approval due to the costly and rigorous process to do so. For, the process involves conducting studies and reporting results to a number of organizations. After which, the product must also undergo a number of tests to support claims related to effectiveness and safety.
Unlike many companies whom mass produce these products, multi radiance super pulsed lasers are produced using innovative technology which delivers direct light energy to tissue increasing circulation and relieving discomfort. In doing so, the light includes wavelengths which allow for better absorption and deeper penetration. As a result, the discomfort is often eliminated for a much longer period of time than when taking medication or obtaining chiropractic adjustments.
Researchers worked with 86 test subjects to determine how light therapies such as phototherapy effected painful areas of the body. The results of a portion of these individuals showed that the technology was more positive than that of associated placebos. After which, participants were asked to return for a one month follow up to determine whether the pain had returned, lessened or subsided completely.
Having discovered that the pain had significantly decreased among most of the individuals involved in the study, researchers were hopeful that FDA approval would be granted. Then, after additional studies showed that the success rate of this new laser light based therapy for pain in the shower and neck was more successful than others, the United States Food and Drug Administration was quick to grant approval. For, in doing so, the organization believed this new treatment would eliminate the need for harsh narcotics and help end what has been becoming an opioid crisis over the last few years in the United States.
When researchers ran studies on test subjects and placebos, results showed that this new laser light based product was more effective than placebos with regards to eliminating discomfort. As a result, the NHN product also received designation as a NHN non-heat, non-thermal based device.
The product emits monochromatic radiation by using light amplification which is coherent and collimated. The process emits energy through wavelengths of infrared or other sources which provide a non-thermal and non-heated effect. In all cases, the product can be used without the need for associated topical or other forms of heat.
While a number of similar products are for sale in the United States, few have obtained FDA approval or have been designated as NHN which recognizes the product as being non-thermal. As such, while a number of the products may be effective, most are lacking the safety requirements of those approved by the FDA.
In most cases, companies avoid undergoing FDA approval due to the costly and rigorous process to do so. For, the process involves conducting studies and reporting results to a number of organizations. After which, the product must also undergo a number of tests to support claims related to effectiveness and safety.
Unlike many companies whom mass produce these products, multi radiance super pulsed lasers are produced using innovative technology which delivers direct light energy to tissue increasing circulation and relieving discomfort. In doing so, the light includes wavelengths which allow for better absorption and deeper penetration. As a result, the discomfort is often eliminated for a much longer period of time than when taking medication or obtaining chiropractic adjustments.
Researchers worked with 86 test subjects to determine how light therapies such as phototherapy effected painful areas of the body. The results of a portion of these individuals showed that the technology was more positive than that of associated placebos. After which, participants were asked to return for a one month follow up to determine whether the pain had returned, lessened or subsided completely.
Having discovered that the pain had significantly decreased among most of the individuals involved in the study, researchers were hopeful that FDA approval would be granted. Then, after additional studies showed that the success rate of this new laser light based therapy for pain in the shower and neck was more successful than others, the United States Food and Drug Administration was quick to grant approval. For, in doing so, the organization believed this new treatment would eliminate the need for harsh narcotics and help end what has been becoming an opioid crisis over the last few years in the United States.
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