AUVON Rechargeable TENS Unit Muscle Stimulator – 24 Modes, Model TU1080, with 8 Electrode Pads

Product Overview

The AUVON TU1080 is a rechargeable transcutaneous electrical nerve stimulation device designed to deliver electrical pulses through adhesive skin electrodes. The configuration identified by ASIN B06ZZ19MS3 includes 24 pre-programmed stimulation choices arranged under six mode groups, adjustable treatment timing, eight square electrode pads, two lead wires, a pad holder, charging cable, storage pouch, and user documentation.

The unit uses a built-in rechargeable lithium-ion battery rather than disposable AA or AAA batteries. Published product information states up to approximately 10 hours of continuous operation under specified conditions and approximately one hour for a full recharge. The electrode system uses standard 2 mm pigtail-style connections, allowing compatible replacement pads to be used when the supplied adhesive electrodes wear out.

TENS devices apply electrical stimulation through electrodes placed on intact skin. They are used for temporary symptomatic relief associated with certain sore and aching muscles rather than to diagnose or cure the underlying cause of pain. Electrode positioning and intensity are important to safe use. Manufacturer warnings state that this unit should not be used by people with implanted cardiac devices and identify additional conditions requiring avoidance or medical consultation.

Product Information

Identification

Physical and Package Information

Product Identifier Summary

Medical and wellness electronics may use several identifiers for cataloging, support, regulatory documentation, and replacement-part matching. Identifiers should be matched to the exact hardware version rather than assumed from visually similar TENS units.

• Model Number: A model number identifies a particular hardware configuration. TU1080 is the current catalog model associated with this product record.
• MPN: A Manufacturer Part Number can distinguish an exact commercial configuration in manufacturer and distributor records. A separate independently verified MPN was not identified.
• UPC: A Universal Product Code is a 12-digit barcode used for retail and inventory identification. A sufficiently verified UPC was not included for this configuration.
• EAN: An EAN is an international retail barcode format within the GTIN system. No independently verified EAN was included.
• GTIN: A Global Trade Item Number identifies commercial trade items across distribution systems. No exact GTIN was included without additional verification.
• ASIN: The ASIN identifies the specific catalog record associated with this AUVON TENS unit.
• ISBN: ISBN identifiers apply to books and certain publications and are not applicable to electrical stimulation devices.

Common Uses

TENS devices are used to provide transcutaneous electrical stimulation through electrodes positioned on the skin. Their intended role is temporary symptomatic management rather than treatment of the underlying cause of an injury or medical condition.

• Temporary relief associated with sore and aching muscles after normal household activities.
• Temporary relief associated with muscle soreness following exercise.
• Electrical stimulation of selected areas of the back, shoulders, arms, or legs when permitted by the device instructions.
• Home electrotherapy sessions performed according to the supplied user manual.
• Portable TENS use when access to electrical outlets is limited by using the internal rechargeable battery.

Maintenance & Care

The control unit, wires, and reusable electrode pads require different types of care. The manufacturer recommends storing the equipment in a cool, dry location and protecting the adhesive surfaces between sessions.

• Turn the stimulator off before removing electrodes or disconnecting lead wires.
• Return electrode pads to their protective film or supplied holder after use.
• Keep the adhesive gel surface free from lint, dust, oils, and other contamination.
• Store the control unit and accessories in a cool, dry location.
• Do not immerse the electronic control unit or lead wires in water.
• Keep charging and lead-wire connectors dry.
• Inspect lead wires for cracking, exposed conductors, or loose connectors before use.
• Replace electrode pads when they no longer adhere evenly to clean skin.
• Charge the unit periodically during long periods of storage; manufacturer guidance specifies charging at least once every three months when the device is not regularly used.
• Use only charging equipment compatible with the device’s documented charging requirements.

Safety Information

TENS stimulation sends electrical current through surface electrodes, so electrode placement and medical-device compatibility are important. The manufacturer’s current warning information should be reviewed before first use.

• Do not use the device if you have a cardiac pacemaker, implanted defibrillator, or another implanted electronic device unless specifically directed by an appropriate medical professional.
• The manufacturer states that the unit should not be used during pregnancy.
• The manufacturer identifies epilepsy among conditions for which the device should not be used without appropriate medical guidance.
• Consult an appropriate healthcare professional before use when a medical condition requires active supervision.
• Do not apply stimulation through the chest or in a configuration that directs electrical current across the heart.
• Do not place electrodes on the front or sides of the neck.
• Use electrodes only on clean, healthy, intact skin.
• Do not place pads over open wounds, irritated skin, infections, or areas with markedly impaired sensation.
• Do not use electrical stimulation while driving, operating machinery, bathing, or performing activities where an unexpected muscle response could create a hazard.
• Stop treatment if stimulation causes burning, severe pain, significant irritation, dizziness, or another unexpected reaction.
• Start with low stimulation intensity and increase only within the instructions supplied for the device.
• Keep the device and accessories out of reach of unsupervised children.

Technical Specifications

Regulatory Information

Transcutaneous electrical nerve stimulators are regulated medical devices in the United States. FDA records include 510(k) clearance K143268 for a family of TENS and powered muscle stimulators manufactured by Shenzhen As-Tec Technology Co., Ltd., with indications covering temporary relief of pain associated with sore and aching muscles and stimulation of healthy muscles.

Public records connected with B06ZZ19MS3 have used several hardware references over the product’s long sales history, including AS-series designations, while the current retail record identifies model TU1080. Because an exact one-to-one regulatory model mapping between TU1080 and a specific FDA-cleared model was not independently established, this page does not describe TU1080 itself as FDA-cleared under a specific 510(k) number.

Product History

The B06ZZ19MS3 product record dates to June 2017 and has remained associated with AUVON rechargeable TENS devices through multiple years of retail availability. The current version is described as a fourth-generation 24-mode TENS unit and uses model designation TU1080.

AUVON has subsequently expanded its electrical-stimulation range with dual-channel, four-output, wireless, touchscreen, TENS/EMS, and larger-battery models. These later units can differ in intensity controls, stimulation programs, pad quantities, connectors, batteries, and supplied cases.

Because multiple AUVON stimulators have similar names and appearances, the exact model number and included accessories should be checked before obtaining replacement cables, manuals, or other model-specific components.

Key Features

• Rechargeable handheld TENS control unit.
• 24 pre-programmed stimulation choices.
• Six primary stimulation-mode groups.
• Adjustable treatment timing.
• Internal lithium-ion battery.
• Battery-level indicator.
• Eight reusable 2 x 2-inch adhesive electrodes.
• Standard 2 mm pigtail-style electrode connections.
• Two lead wires.
• Electrode pad storage holder.
• Compact storage pouch.
• USB charging capability.

Package Contents

• One AUVON TU1080 TENS unit.
• Eight 2 x 2-inch square electrode pads.
• Two lead wires.
• One electrode pad holder.
• One USB Type-C charging cable.
• One storage pouch.
• One user manual.

Compatibility

The unit uses removable lead wires and adhesive electrodes. Replacement-pad compatibility depends primarily on the electrode connector type and the electrical-stimulation device for which the pads are designed.

• Compatible with suitable TENS electrode pads using a 2 mm pigtail connection.
• AUVON sells replacement electrodes in several shapes and sizes using compatible connector systems.
• Replacement pads should be intended for TENS or compatible electrotherapy equipment.
• Electrodes from snap-style systems should not be assumed compatible without the correct connector arrangement.
• Charging cables and power equipment should match the specific hardware revision.
• The device does not require a smartphone application for ordinary operation.

Frequently Asked Questions

What product is B06ZZ19MS3?

B06ZZ19MS3 identifies an AUVON rechargeable TENS unit sold with 24 stimulation choices and eight reusable 2 x 2-inch electrode pads.

What is the current model number?

The current catalog record identifies the product as model TU1080. Older public regulatory and adverse-event records associated with the product family may contain different AS-series hardware designations.

Is this a TENS or EMS machine?

The current AUVON product listing identifies this configuration primarily as a TENS unit. AUVON sells separate 3-in-1 and explicitly labeled TENS/EMS models, so EMS functions should not be assumed merely because similar AUVON products include them.

What does TENS mean?

TENS stands for transcutaneous electrical nerve stimulation. Electrical pulses travel from the control unit through surface electrodes placed on the skin.

Does the device cure the cause of pain?

No. TENS is used for temporary symptomatic relief in appropriate circumstances and does not diagnose or eliminate the underlying cause of pain.

How many stimulation modes are available?

The unit provides 24 pre-programmed choices arranged within six main mode groups.

Can the treatment duration be adjusted?

Yes. The current product information identifies adjustable timing as part of the operating controls.

Does it use disposable batteries?

No. The unit contains a rechargeable lithium-ion battery.

How long does the battery operate?

The manufacturer states that a fully charged battery can provide up to approximately ten hours of continuous operation. Actual runtime can vary with settings, battery age, and use conditions.

How long does charging take?

The published charging information states approximately one hour for a full recharge under the specified charging conditions.

Does the unit show remaining battery power?

Yes. A battery or power indicator provides information about the remaining charge.

What size electrode pads are included?

The package contains eight square pads measuring approximately 2 x 2 inches each.

Are the electrode pads reusable?

Yes. They are reusable self-adhesive electrodes. Useful life depends on skin preparation, storage, adhesive contamination, and handling.

How should electrode pads be stored?

They should be returned to their protective surface or supplied holder after use and stored in the pouch or another clean environment to limit contamination of the adhesive gel.

When should TENS pads be replaced?

Replace pads when they no longer adhere evenly, the conductive surface becomes damaged or contaminated, or stimulation becomes uneven despite correct placement and intact lead wires.

What connector do replacement pads need?

The current product information identifies a 2 mm pigtail-style electrode connection. Replacement pads should match that connection and be intended for compatible electrotherapy equipment.

Can larger electrode pads be used?

Compatible AUVON replacement electrodes are available in additional sizes. The connector and intended stimulation application should be checked before substitution.

Where can the electrodes be placed?

Placement depends on the body area and intended use. The supplied manual should be followed because some locations, including the front or sides of the neck and current paths across the chest, require avoidance.

Can electrodes be placed directly over the spine?

Electrode placement should follow the manufacturer’s diagrams rather than being improvised. Pads are generally positioned around the target area according to the manual rather than placed wherever discomfort is felt.

Can TENS be used on broken skin?

No. Electrodes should be placed on healthy, clean, intact skin rather than cuts, rashes, infections, or open wounds.

Can TENS cause skin irritation?

Yes. Adhesive gel and electrical stimulation can cause redness or irritation in some users. Stop use if significant burning, persistent redness, blistering, or another unexpected skin reaction occurs.

Should the intensity hurt?

Electrical stimulation may produce a noticeable tingling or pulsing sensation, but severe pain or burning is not an intended response. Treatment should be stopped if an unexpectedly painful sensation occurs.

Should intensity start at the maximum level?

No. Stimulation should begin at a low level and be increased gradually according to the device instructions and individual comfort.

Can someone with a pacemaker use this TENS unit?

The manufacturer’s warnings state that the unit should not be used by people with a cardiac pacemaker, implanted defibrillator, or another implanted electronic device unless specifically directed under appropriate medical supervision.

Can the unit be used during pregnancy?

The manufacturer’s instructions state that pregnant users should not use this device without appropriate medical guidance.

Can someone with epilepsy use it?

Epilepsy is identified in the manufacturer’s warnings. A person with epilepsy should obtain appropriate medical guidance rather than using the device without supervision.

Can it be used while sleeping?

Electrical stimulation should be used only while the person can monitor the sensation and electrode condition. Unsupervised use during sleep should be avoided unless specifically permitted by the device instructions and a healthcare professional.

Can it be used while driving?

No. Electrical stimulation should not be used while driving or operating machinery because unexpected sensations or muscle responses can create a safety hazard.

Can the unit be used in a bath or shower?

No. Electrical stimulation equipment should not be used in water or while bathing or showering.

Can the device be charged from a computer?

The manufacturer’s maintenance information indicates that USB charging can be performed through compatible USB power equipment, including a computer connection when appropriate.

How should the unit be stored if it is rarely used?

Keep it in a cool, dry location and periodically recharge the battery. AUVON recommends charging the device at least once every three months during extended periods of non-use.

Does it require an app or Bluetooth?

No. The TU1080 is controlled directly from its own interface and does not require a smartphone application for normal TENS operation.

Is TU1080 FDA approved?

The FDA regulates TENS devices through medical-device pathways rather than using the term “FDA approved” for most products of this type. FDA records document cleared TENS and powered muscle-stimulation device families from manufacturers connected with earlier AUVON hardware, but an exact TU1080-to-510(k) mapping was not independently established for this page.

What warranty applies?

The current product information specifies a 12-month warranty, subject to the manufacturer’s applicable coverage terms and exclusions.

Buying Considerations

TENS devices should be evaluated according to their intended use, controls, electrode system, safety warnings, and compatibility with a user’s medical circumstances. More stimulation modes do not necessarily mean that every program is appropriate for every person or body area.

• Review the contraindications and warnings before first use.
• Confirm model TU1080 when locating replacement manuals or accessories.
• Check the 2 mm electrode connector when selecting replacement pads.
• Consider how often replacement adhesive pads will be required.
• Consider rechargeable-battery operation when the unit will be used away from fixed power sources.
• Do not interpret temporary symptom relief as diagnosis or treatment of an underlying injury or disease.
• Persistent, unexplained, severe, or worsening pain should be medically evaluated rather than managed only with electrical stimulation.
• People with implanted electronic devices or significant medical conditions should obtain appropriate medical guidance before considering TENS use.

Customer Feedback Summary

This section summarizes recurring themes in publicly available customer feedback about the AUVON rechargeable TENS unit. These observations are subjective user experiences and are not verified medical outcomes or technical specifications.

Positive feedback commonly focuses on the compact control unit, rechargeable battery, range of stimulation patterns, and ability to adjust treatment without carrying disposable batteries. Users also frequently mention the supplied pouch and electrode holder as useful for keeping the wires and pads together between sessions.

The adhesive electrodes receive generally positive comments when they are new and stored carefully. Users commonly report that cleaning the skin before placement and protecting the gel surfaces from dust helps extend useful pad life. Adhesion gradually declines with repeated use, making replacement pads a recurring maintenance item.

The large number of stimulation patterns receives mixed reactions. Some users value having multiple sensations available, while others report that the differences between programs are not immediately obvious and require experimentation within the supplied instructions.

Reported limitations include wires becoming tangled during storage, pads eventually losing adhesion, and differences in perceived intensity between body areas. Some public reports also describe skin redness, burning sensations, or unexpectedly strong stimulation. Such experiences are not universal, but they reinforce the importance of correct pad contact, low initial intensity, intact electrodes, and stopping use if an abnormal reaction occurs.

Related Products

• AUVON 20-Mode Dual Channel TENS Unit.
• AUVON 24-Mode TENS/EMS Muscle Stimulator.
• AUVON 4-Output TENS Unit.
• AUVON Wireless TENS Unit.
• AUVON Touchscreen TENS Unit.
• AUVON 2 x 2-inch replacement electrode pads.
• AUVON 2 x 4-inch replacement electrode pads.
• AUVON mixed-size TENS electrode pad sets.
• AUVON compatible replacement lead wires.

Last Updated

August 10, 2026