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FDA Clearance and Other Government Approvals

The drug free ActiPatch is U.S. Government Food and Drug Administration (FDA) cleared for use in reducing edema (swelling) following blepharoplasty and has no known side effects. The product is also approved by Health Canada for the relief of pain in musculoskeletal complaints and is widely available in pharmacies across Canada. The European Union has also approved ActiPatch as a Class II pulsed electromagnetic medical device as have numerous other international regulatory agencies. The technology, dosage and effectiveness have been validated by the State University of New York and in numerous scientific and medical studies and papers.

“I used ActiPatch on my shoulder after rotator cuff repair when neither Lortab nor Mepergan gave me any pain relief. After wearing the ActiPatch for 12 hours, I did not take even one more pain pill. The swelling was reduced and motion in my hand improved. After wearing the shoulder brace for six weeks post- op, upon removal I required no therapy to regain motion in my arm. My doctor was pleased. Amazed, but pleased!”

—Elaine L. Argent, L.P.N.