FDA-Cleared Wearable · Pulsed Shortwave Therapy · Available over-the-counter (OTC)

ActiPatch® is an FDA 510(k) cleared (K192234), drug-free bioelectric wearable that delivers pulsed shortwave therapy (PSWT) at 27.12 MHz for over-the-counter adjunctive treatment of musculoskeletal pain, including muscle and joint pain. Can be used alongside other treatments. No prescription needed.

ActiPatch (1 unit) device

FDA-Cleared Wearable · Pulsed Shortwave Therapy · Available over-the-counter (OTC)

ActiPatch® (1 unit)

ActiPatch® is an FDA 510(k) cleared (K192234), drug-free bioelectric wearable that delivers pulsed shortwave therapy (PSWT) at 27.12 MHz for over-the-counter adjunctive treatment of musculoskeletal pain, including muscle and joint pain. Can be used alongside other treatments. No prescription needed.

$39.99
Free shipping on ActiPatch® single, double, and triple packs (US addresses only, through December 31, 2026)

Choose your pack

Every device provides 720 therapy hours, with adhesive tape included. Nothing to charge or pair.

1

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Buying questions

Which pack should I choose?
All packs contain the same ActiPatch® device. Choose a single pack for one device, a double pack for two, or a triple pack for three. Compare the price per device shown above.
Do I need an account to order?
No. You can check out as a guest without creating an account.
Do you ship outside the US?
We ship only to US addresses and US territories.
Is there a free sample or trial?
No free samples. Every purchase is covered by the 30-day money-back guarantee. Request it within 30 days of delivery; the device does not need to be sent back. 30-day money-back guarantee.
How long does one device last?
Each ActiPatch® device provides 720 therapy hours. Placement and daily wear guide.

Testimonials

Excerpts from sourced personal accounts, separate from customer reviews. Individual results vary.

Portrait of Tom Dundon
“I used ActiPatch® on my knees. For the first time in years I went shopping with my wife and I didn’t have to find a seat because my knees were hurting too much.”
Tom DundonPublished by BioElectronics Corporation
Portrait of Pamela Orchard
“I slept well and was amazed by the reduction of pain in my lower back.”
Pamela OrchardPublished by BioElectronics Corporation
Portrait of Pauline Levi-Tilley
“ActiPatch® is just brilliant. It is the only thing that has taken my chronic shoulder pain away.”
Pauline Levi-TilleyPublished by BioElectronics Corporation
Portrait of Catriona McDiarmid
“I bought ActiPatch® at Boots as I had so much hip and back pain and physio wasn’t helping. The ActiPatch® really does work. Money well spent. I’m a happy bunny!”
Catriona McDiarmidPublished by BioElectronics Corporation

How to Use ActiPatch®

1

Position over pain

Place the device loop directly over the source of your pain.

2

Secure with tape

Use the included tape to hold the loop in place over the intended area.

Or wear it over a thin layer of clothing. Avoid thick fabric between the device and the skin.

3

Switch on and follow directions

Press the on/off button, then follow the package directions for use and wear duration.

Open or download ActiPatch® instructions (PDF)

Official BioElectronics Corporation directions for use, including placement, activation, care and safety precautions. Opens on the manufacturer's website in a new tab. Use your PDF viewer's download button to save a copy.

Product Details

Common uses

Back PainKnee PainKnee OsteoarthritisNeck PainShoulder PainHip PainFoot PainHeel Pain (Plantar Fasciitis)ArthritisSports InjuriesMuscle & Joint Pain

What's Included

1 ActiPatch® device720 hours each
Adhesive tapeIncluded in pack
CR2032 batteryIntegrated
Ready to useNothing to connect

Technical Specifications

Therapy type
Pulsed Shortwave Therapy
Frequency
27.12 MHz
Pulse rate
1,000 pulses per second
Treatment area
110 cm²
Operation time
720 therapy hours
Battery
Integrated CR2032 battery
Device weight
9.5 g

At a Glance

Different from TENS

A self-contained wearable—no electrode pads or lead wires to manage. Designed to operate without perceptible heat or tingling from the device.

Drug-Free

Contains no medicine or active drug ingredient.

FDA 510(k) Cleared

FDA-Cleared Technology

FDA-cleared (510(k) K192234) for over-the-counter adjunctive treatment of musculoskeletal pain, meaning it can be used alongside other treatments.

View the official record

Open the FDA's public K192234 record and confirm the clearance details directly.

Evidence presented in context

Product and mechanism details on this page stay within the cleared over-the-counter (OTC) indication. Individual experiences vary; product information is not medical advice.

Who should not use ActiPatch®

Review before use. See the package insert for full contraindications, warnings and precautions.

  • 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.

From the evidence library

What does the evidence show?

ActiPatch® is FDA-cleared (510(k) K192234) for over-the-counter adjunctive treatment of musculoskeletal pain. These counts cover selected ActiPatch® clinical publications, not laboratory studies or studies of other devices. Study conditions and protocols differ, and individual results vary.

Published records
6
Each paper counted once
Randomized controlled trials
3
Library design label: RCT
Publication years
2012–2021
Earliest to latest record
What do clearance and research tell us?

FDA clearance identifies the device's permitted use; it is not an endorsement or a guarantee of results. These pain trials do not establish improved circulation, tissue repair, or reduced inflammation as ActiPatch® outcomes.

Read the FDA clearance record (opens in a new tab)

How soon might I notice a difference?

Individual experiences vary. Many people report noticing relief within a few hours; for some, it can take up to four days of consistent wear. Keep following the package directions and do not change medications or prescribed care without speaking with your healthcare provider.

RCT2016 · Rheumatology (Oxford)

Pulsed Electromagnetic Fields in Knee Osteoarthritis: A Double-Blind Placebo-Controlled Randomized Clinical Trial

Bagnato GL, Miceli G, Marino N, Sciortino D, Bagnato GF

In a four-week, randomized, double-blind, placebo-controlled ActiPatch® trial in knee osteoarthritis, 66 people were randomized and 60 completed the study. The investigators reported improvements in pain and physical function compared with placebo. Participants wore the device 12 hours a day.

Read the source publication(opens in a new tab)
RCT2012 · Journal of Foot and Ankle Surgery

Pulsed Radiofrequency Electromagnetic Field Therapy: A Potential Novel Treatment of Plantar Fasciitis

Brook J, Dauphinee DM, Korpinen J, Rawe IM

A seven-day, randomized, double-blind, placebo-controlled trial studied nightly use for plantar fasciitis. Among 70 participants who completed the study, the active-treatment group reported a greater reduction in morning pain than the placebo group.

Read the source publication(opens in a new tab)

Evidence describes study results, not a promise of the same result for everyone. This is not medical advice.

Explore the full evidence library

Frequently Asked Questions

Read the package insert for full contraindications, warnings and precautions. Do not use if you are pregnant or think you may be pregnant, or if you have a cardiac pacemaker, implanted defibrillator, or other active implanted metallic or electronic device. Not for use by or on children under 17. If you are under a doctor's care, consult your doctor before use.

It means ActiPatch® can be used alongside other treatments for musculoskeletal pain, including muscle and joint pain. Do not stop or change prescribed treatment without speaking with your healthcare professional.

No. ActiPatch® is available over-the-counter (OTC). It is FDA 510(k)-cleared under K192234 for adjunctive treatment of musculoskeletal pain.

Each ActiPatch® device provides 720 therapy hours. If it runs continuously, that is approximately 30 days; intermittent use spreads those operating hours over a longer calendar period.

No. The CR2032 battery is integrated and is not designed for user replacement or charging. Follow the package directions for use and end-of-use handling.

ActiPatch® is a self-contained, drug-free wearable with nothing to charge or pair, and it is designed for comfortable, continuous wear with no tingling sensation from the device. The indicator light confirms that the device is operating.

Individual experiences vary. Many people report noticing relief within a few hours; for some, it can take up to four days of consistent wear. Keep following the package directions and do not change medications or prescribed care without speaking with your healthcare provider.

Individual experiences vary. Many people report noticing relief within a few hours; for some, it can take up to four days of consistent wear. Wear ActiPatch® as the package directions describe for the hours and days of your first week, and do not change medications or prescribed care without speaking with your healthcare provider.

ActiPatch® is designed for comfortable, continuous wear, so it can be worn while you sleep when positioned as the package directions describe. If the tape or wrap irritates your skin, stop using it and review the package directions or ask a healthcare professional.

Yes. Use one ActiPatch® device per painful area, with each loop positioned over its own site of pain as the package directions describe.

Not feeling anything is expected. ActiPatch® is designed for comfortable, continuous wear with no tingling sensation from the device. The indicator light confirms that the device is operating.

ActiPatch® is generally eligible for purchase with a health savings account (HSA) or flexible spending account (FSA). Eligibility depends on your plan, so confirm with your plan administrator.

Electrome does not bill insurance or Medicare for ActiPatch®. Check with your insurer about whether any reimbursement is available. RecoveryRx® is a prescription device available through healthcare providers.

ActiPatch® contains no medicine or active drug ingredient. If you have questions about using any device with your medicines or current care, ask a clinician or pharmacist.

ActiPatch® is developed and manufactured by BioElectronics Corporation and marketed by Electrome under an exclusive license. The manufacturer-sourced testimonials link to their original publications. They describe individual experiences, and results vary. They are not a substitute for medical advice.

Position the loop over the site of pain. Wear it directly on the skin with the included tape or a wrap, or over a thin layer of clothing such as a t-shirt or leggings. Avoid thick fabric between the device and the skin. Follow the package directions and do not wear the device in water.

Free shipping on ActiPatch® single, double, and triple packs (US addresses only, through December 31, 2026). Other products ship at the rate shown at checkout. Applicable tax and the final order total are shown at checkout before payment.

What customers say

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Verified customer ·

★★★★★

Easy purchase

I’m looking forward to using it

Anyone who has used ActiPatch® may review it. Individual results vary. We offer no incentives for reviews; positive and negative reviews publish under the same rules. Review policy