GrivaMax initiated the process of obtaining FDA certificate for the latest model

NEW YORK - May 7, 2018 - PRLog -- GrivaMax started the certification process for the newest model, GRIVAMAX LASER CAP 148. As a result, the entire line of hair restoration products will have a Certificate from the Food and Drug Administration (FDA). Right after receiving it, the latest model will be available for sale in the US.

We offer portable devices that effectively treat hair loss and alopecia (androgenetic alopecia) and restore the hair structure in men and women.

The uniqueness of low-level laser therapy (Low-Level Laser Therapy, 650nm) is that it can be used both for the treatment of baldness and for hair restoration. You can use LLLT by itself and in combination with other methods. In this case, Low-Level Laser Therapy enhances the therapeutic effect.

Today we are working on getting certification for the GRIVAMAX LASER CAP 148. The device will help to maintain beautiful and healthy hair, just by using it a few minutes a day. Our product guarantees shiny and vibrant hair. GRIVAMAX LASER CAP 148 will help restore hair that has been damaged by sunlight, salt water, dyes, flat ironing, hair dryers, chlorinated pool water, or the excessive use of styling products. More information at www.grivamax.com.

Why is the FDA certificate important?
A certificate from the US Food and Drug Administration ensures that you purchase a high-tech product manufactured according to GMP standards. All accessories are made from safe materials. An FDA certificate is another proof of low-level laser therapy efficiency.