Drug-Free Pain Relief: Where a Bioelectric Wearable Fits
By Electrome Corporation · Published October 5, 2026
FDA 510(k) K192234 indication: "adjunctive treatment of musculoskeletal pain". ActiPatch is an FDA-cleared, over-the-counter bioelectric wearable using Pulsed Shortwave Therapy (PSWT). It contains no active drug ingredient and is used alongside other care.
Shop ActiPatchWhat does drug-free mean?
ActiPatch is a wearable pain relief device, not a medication. Drug-free means it contains no active drug ingredient. For people exploring pain relief without medication, that describes the device, not advice to stop medication or other care.
Bioelectric names the device type and does not extend its cleared uses. ActiPatch uses PSWT at 27.12 MHz without electrode pads or lead wires and without perceptible heat or tingling.
Where does it fit alongside care?
ActiPatch does not replace opioids or prescribed medication. If you are under a doctor's care, consult your doctor before use. Never change medication without a clinician.
Adjunctive means alongside other treatments. No prescription is needed for ActiPatch, but over-the-counter availability does not mean it is suitable for everyone.
What does the evidence establish?
Published ActiPatch-related PSWT trials include Bagnato and colleagues' knee osteoarthritis study (2016) and Brook and colleagues' plantar fasciitis heel-pain study (2012). They investigated outcomes in their own study populations. Observational registries describe reported experience but do not establish comparative effectiveness.
Individual results vary. Many people report noticing a difference within the first few weeks of consistent use. Read the science overview for study designs and limitations.
Who should not use it?
Do not use if you have a cardiac pacemaker, implanted defibrillator, or other active implanted metallic or electronic device.
Do not use if you are pregnant or think you may be pregnant.
Not for use by or on children under 17.
Do not use for sudden or unexplained pain, or if the cause of the pain is unknown. Not for pain deep in the body such as the chest or stomach, and not for cancer-related pain.
The device is not sterile. Do not place it in direct contact with open wounds.
If pain does not improve after 7 days of use, stop and consult a doctor. If you are under a doctor's care, consult your doctor before use.
Read the supplied package insert before use.
Frequently asked questions
Is ActiPatch a medication?
No. ActiPatch is an FDA-cleared PSWT device for adjunctive treatment of musculoskeletal pain, not a medication.
Does it contain any drug?
No. ActiPatch contains no active drug ingredient.
Can I use it with my medications?
ActiPatch does not replace opioids or prescribed medication. If you are under a doctor's care, consult your doctor before use. Never change medication without a clinician.
Do I need a prescription?
No. ActiPatch is available over-the-counter. Read the precautions and consult your doctor before use if you are under a doctor's care.
Educational information only. ActiPatch is FDA 510(k) cleared (K192234) for over-the-counter (OTC) adjunctive treatment of musculoskeletal pain. Read the package instructions and consult a clinician about persistent or worsening pain.