One of LifeWave’s primary goals is to have our products classified consistently across the globe. With that, we have some positive news regarding IceWave’s classification in Europe.

Last year, the United States FDA created a new category called “General Wellness” for Low Risk Devices. As many of you know, we switched our regulatory registration in the United States over to this new category because of the advantages it provides.

We have had a similar opportunity present itself in the EU. As a result, IceWave will now be classified as a GPSD (General Product Safety Device), the EU equivalent for this FDA category.

PLEASE NOTE: All product claims will remain the same with this change.

Please pass this important news along to your teams, and thanks for your continued support!