FDA Registered Cosmetic Device – The Personal Hair Therapy Laser from Nutreve

Nutreve Personal Hair Therapy Laser - FDA Registered Cosmetic Device

FDA Registered Cosmetic Device – The Personal Hair Therapy Laser from Nutreve

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50% of all men and 1 in 4 women experience forms of thinning hair and or hair loss to varying degrees. The FDA has recognized the value of Low Level Laser Light Therapy in treating this common problem.

The Nutreve Personal Hair Therapy Laser is the most state-of-the-art laser hair therapy device in its class, available anywhere.

Nutreve Personal Hair Therapy Laser is the most state-of-the-art hand-held laser hair therapy deviceIt is designed and manufactured in the United States of the highest quality components for long lasting hair therapy treatments for men & women.

Nutreve has complied with the registration requirements for the device with the Food & Drug Administration, Accession # 1220386-000.  Additionally, it is CE Certified, RoHs compliant and is manufactured in an ISO – 9001 manufacturing standards facility.  Nutreve is diligent in maintaining the highest standards for components and manufacturing for all its products.

To Understand More About this Hair Loss Treatment Technology Visit

Thinning Hair Clinical Study Laser Hair Therapy for Hair Increased Hair Count

Frequently Asked Question about Hair Loss and the Nutreve products

What is Pulsed Wave Technology and Why Should You Care?

The Nutreve “Try It Satisfaction Promise” Guarantee

If I Order a Nutreve Hair Loss Package, What do I Get Exactly?

Visit Craig Froley, Owner Nutreve International at Google+

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FDA Registered Cosmetic Device
Nutreve Personal Hair Therapy Laser is a Class 3r Cosmetic Device. Not intended for medical use.