When it comes to overcoming painful joints, it can often be difficult to find the right treatment option. In most cases, individuals end up taking harsh narcotics and receiving painful injections either of which can become addictive. Now that there is a new FDA Approved Laser For Pain, this may no longer be the case.
After a series of tests with subjects determined that the laser was more effective than a placebo with regards to reducing this type of discomfort, the FDA approved the laser for use in pain management. As such, the NHN product classified as a FDA 510(k) clearance allows patients and clinicians a safer and more effective drug-free method of pain management.
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.
There are a number of similar laser and light based pain relieving products for sale around the world. While this is the case, very few have received approval in the United States or other countries. For, most have never been tested for safety or effectiveness. As such, these products can not be designated as non-heated or non-thermal such as this new light based laser device.
Companies often avoid the steps necessary to obtain United States Federal Drug and Administration approval. For, the process can be extremely long and costly. As such, a number of companies will simply obtain a local registration and trademark and move forward with sales and distribution.
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.
During these research studies, researchers worked with eighty six individuals to determine how light therapies such as phototherapies and others effected non-specific painful areas in the knee. Results associated with twelve individuals showed that the therapies were effective in easing and at times eliminating pain. After which, those twelve individuals were re-assessed during a one month follow up with researchers.
Once having discovered the discomfort had significantly decreased among the majority of the test subjects, FDA approval was pretty much assured. While this was the case, the studies went on to determine the success rate of this new laser based therapy on pain in the shoulder and neck which resulted in the final round of studies and FDA approval. As a result, a number of individuals whom had to take harsh narcotics, make regular visits to a chiropractor or receive painful injections on a regular basis, no longer have to do so.
After a series of tests with subjects determined that the laser was more effective than a placebo with regards to reducing this type of discomfort, the FDA approved the laser for use in pain management. As such, the NHN product classified as a FDA 510(k) clearance allows patients and clinicians a safer and more effective drug-free method of pain management.
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.
There are a number of similar laser and light based pain relieving products for sale around the world. While this is the case, very few have received approval in the United States or other countries. For, most have never been tested for safety or effectiveness. As such, these products can not be designated as non-heated or non-thermal such as this new light based laser device.
Companies often avoid the steps necessary to obtain United States Federal Drug and Administration approval. For, the process can be extremely long and costly. As such, a number of companies will simply obtain a local registration and trademark and move forward with sales and distribution.
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.
During these research studies, researchers worked with eighty six individuals to determine how light therapies such as phototherapies and others effected non-specific painful areas in the knee. Results associated with twelve individuals showed that the therapies were effective in easing and at times eliminating pain. After which, those twelve individuals were re-assessed during a one month follow up with researchers.
Once having discovered the discomfort had significantly decreased among the majority of the test subjects, FDA approval was pretty much assured. While this was the case, the studies went on to determine the success rate of this new laser based therapy on pain in the shoulder and neck which resulted in the final round of studies and FDA approval. As a result, a number of individuals whom had to take harsh narcotics, make regular visits to a chiropractor or receive painful injections on a regular basis, no longer have to do so.
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