Vaginal RF Machine

  • ✓ Factory Direct
  • ✓ Pre-Shipment Inspection & Testing
  • ✓ Operator Training & Protocols
  • ✓ 1-Year Warranty + Lifetime Remote Support
  • ✓ Spare Parts & Repair Support
  • ✓ OEM / Distributor Support

Professional Vaginal RF Systems
Compare professional radiofrequency systems with internal and external applicators for regulated intimate-care workflows. Review RF frequency, temperature controls, applicator design, cooling, hygiene requirements, and market authorization before selecting a device.
Internal & External Applicators • Adjustable RF Output • Temperature Management • Professional Training

Professional Vaginal and External Vulvar RF Systems

Professional intimate radiofrequency systems use controlled RF energy through specialized internal or external applicators. Available configurations include a 5 MHz system for regulated internal and external workflows and an external-only vulvar RF system. These machines differ in application area, RF frequency, power controls, applicator design, temperature management, cooling, consumables, and hygiene requirements. Providers should confirm the exact device configuration and destination-market authorization before offering any intimate RF service.
Professional-use notice: Internal and external intimate RF procedures may be regulated medical services. Treatment suitability, permitted claims, provider qualifications, informed consent, cleaning requirements, and clinical supervision depend on the exact device and local regulations.

Compare Available Intimate RF Systems

FeminaRF Internal & External 5 MHz RF System — 180W

A professional 5 MHz radiofrequency system with dedicated configurations for regulated internal vaginal and external vulvar applications. Listed features include 180W power, touchscreen operation, built-in cooling, adjustable RF controls, and replaceable treatment tips.

RevivaV™ External Vulvar RF System

A professional external-use radiofrequency platform for compatible vulvar treatment areas. This model does not include an internal vaginal applicator and must not be presented as an internal vaginal RF system.

FeminaRF vs RevivaV RF System

Feature FeminaRF 5 MHz RF System RevivaV External Vulvar RF System
Application Type Internal vaginal and external vulvar configurations External vulvar application only
Internal Applicator Included; confirm final tip configuration Not included
External Applicator Included Dedicated external RF applicator
Listed RF Frequency 5 MHz Confirm before ordering
Listed Power 180W Confirm RF output and electrical input separately
Cooling Built-in cooling is listed Confirm cooling and temperature-management method
Tips and Consumables Replaceable treatment tips; confirm included quantity and single-use status Confirm external applicator covers, conductive medium, and replacement parts
Primary Buyer Qualified providers requiring both internal and external configurations Qualified providers offering external-only intimate-care workflows
Key Verification Tip design, temperature controls, hygiene validation, and internal-use authorization External-use labeling, RF specifications, temperature controls, and applicator design
The FeminaRF product page should describe the device as an RF system unless a separate HIFU generator and HIFU applicator are actually included. The RevivaV product page must clearly state “external use only” and “no internal vaginal applicator.”

How the Two RF Configurations Differ

Internal Vaginal RF Applicator

Available with the FeminaRF system. Internal application requires model-specific insertion, contact, movement, dwell-time, output, temperature, and hygiene protocols.

External Vulvar RF Applicator

Available with both systems. External applicators are designed for compatible external tissue and may require different parameters from internal applicators.

External-Only Configuration

RevivaV is designed only for external vulvar application. It must not be inserted into the vaginal canal or promoted for internal vaginal treatment.

Temperature Management

Confirm where temperature is measured, how frequently it updates, whether output adjusts automatically, and what happens when the temperature limit is reached.

Cooling System

Applicator cooling may help manage surface temperature but does not replace temperature monitoring, correct movement, conservative settings, or operator supervision.

Replaceable Tips and Covers

Internal and external patient-contact components require clear single-use, cleaning, high-level disinfection, sterilization, storage, and replacement instructions.

Understanding the Limits of Intimate RF

RF Is Not Pelvic Floor Stimulation

Radiofrequency primarily generates controlled tissue heating. It does not directly induce repeated pelvic floor muscle contractions like EMS or electromagnetic stimulation equipment.

External RF Is Not Internal RF

An external vulvar applicator cannot be assumed to treat internal vaginal tissue. Each product must remain within its documented application area.

Symptoms Require Medical Assessment

Dryness, pain, bleeding, discharge, urinary symptoms, sexual discomfort, and postpartum concerns may have multiple causes and require appropriate medical evaluation.

Results Cannot Be Guaranteed

Do not guarantee tightening, lubrication, symptom relief, sexual-function improvement, treatment duration, or a fixed number of required sessions.

Vaginal RF Machine

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How to Choose an Intimate RF System

The correct system depends first on whether the provider requires an internal and external configuration or an external-only platform. Buyers should then evaluate RF specifications, applicator design, temperature controls, hygiene validation, consumables, operator requirements, and market authorization.

Choose FeminaRF for Internal and External Workflows

Select FeminaRF when both internal vaginal and external vulvar applicators are required and the provider is qualified and legally permitted to perform internal procedures.

Choose RevivaV for External-Only Services

Select RevivaV when the intended service menu is limited to compatible external vulvar RF applications and no internal vaginal probe is required.

Verify RF Output

Confirm operating frequency, measured RF output, adjustment range, electrode configuration, waveform, treatment modes, and the difference between rated input power and delivered RF power.

Evaluate Thermal Controls

Review temperature-sensor location, display accuracy, maximum-temperature limit, alarms, automatic output adjustment, contact monitoring, cooling, and emergency stop.

Review Hygiene Requirements

Request written instructions for single-use tips, applicator covers, conductive media, cleaning, high-level disinfection, sterilization, storage, and reusable-part lifespan.

Confirm Regulatory Status

Verify the intended use, permitted claims, device classification, registration, labeling, provider qualifications, and applicable regulations in the destination market.

Specifications to Confirm Before Ordering

Specification What to Confirm
Application Area Internal and external, or external-only; this must be stated clearly in the quotation and manual
RF Frequency Exact operating frequency, tolerance, waveform, and model-specific technical documentation
RF Output Measured energy output at the applicator rather than only the machine’s electrical input rating
Electrode Configuration Monopolar, bipolar, or multipolar design and whether a return electrode is required
Internal Applicator Availability, dimensions, insertion markings, electrode location, temperature sensor, tips, and covers
External Applicator Supported external areas, electrode size, temperature sensor, controls, and cleaning method
Temperature Control Sensor location, measurement accuracy, limit settings, cutoff, alarm, and automatic adjustment
Cooling Cooling method, coolant requirements, maintenance schedule, temperature range, and fault detection
Consumables Tip and cover quantity, single-use status, conductive medium, replacement cost, and availability
Cleaning and Disinfection Validated cleaning products, contact time, disinfection level, storage, and reusable-part lifespan
Voltage and Plug 110V or 220V configuration and the correct destination-country plug
Regulatory Documentation Exact model, manufacturer, intended use, certificate scope, registration number, and permitted claims
Warranty Main-unit, applicator, cooling component, cable, accessory, and consumable coverage

Professional Screening and Operation

Before Treatment

  • Confirm that the operator is legally qualified to provide the intended procedure.
  • Complete an appropriate medical, gynecological, medication, implant, and treatment-history assessment.
  • Investigate unexplained pain, bleeding, discharge, lesions, dryness, or urinary symptoms.
  • Confirm pregnancy status and the presence of an IUD, mesh, metal, or electronic implants.
  • Inspect the applicator, cable, electrode, sensor, cooling system, covers, and treatment tips.
  • Verify whether the selected applicator is intended for internal or external use.
  • Obtain appropriate informed consent covering risks, uncertainties, alternatives, and aftercare.

During and After Treatment

  • Follow the exact model’s contact, movement, output, temperature, and time instructions.
  • Never insert an external-only RevivaV applicator into the vaginal canal.
  • Continuously monitor temperature, sensation, applicator position, and tissue response.
  • Do not increase output solely to create stronger heat or faster visible change.
  • Stop immediately for burning, sharp pain, bleeding, numbness, blistering, or equipment alarms.
  • Provide model-specific aftercare and adverse-event reporting instructions.
  • Document the applicator, tip lot, settings, temperature, duration, area, and response.
Safety notice: Potential risks of energy-based intimate procedures may include burns, pain, scarring, infection, altered sensation, painful intercourse, and persistent symptoms. Suitability must be determined by an appropriately qualified healthcare professional using the exact device instructions and applicable regulations.

Claims That Require Model-Specific Evidence

The following statements should not appear as standard category benefits unless they are permitted and supported for the exact device in the destination market:
  • Treats urinary incontinence
  • Strengthens pelvic floor muscles
  • Treats vaginal dryness or menopause symptoms
  • Improves sexual satisfaction or sensitivity
  • Restores vaginal health
  • Produces permanent vaginal tightening
  • Provides immediate or guaranteed results
  • Is pain-free, risk-free, or suitable for every woman
  • Requires no medical assessment
  • Is FDA cleared without a matching model-specific clearance number
A safer product statement is: “Available applications, treatment parameters, potential outcomes, risks, and provider requirements depend on the exact device documentation, regulatory authorization, professional assessment, and individual response.”

Equipment Supply and Support

Operator Training

Receive guidance covering system setup, applicator identification, temperature controls, consumables, cleaning, maintenance, and basic troubleshooting.

Warranty Coverage

Standard support includes a one-year warranty for the main unit. Confirm separate coverage for applicators, cables, cooling components, and accessories.

Technical Support

Access remote troubleshooting and assistance with compatible applicators, tips, covers, cables, cooling components, and replacement parts.

OEM and Distributor Support

Discuss eligible branding, interface language, manuals, packaging, consumables, documentation, and distributor configurations.
  • MOQ of one unit
  • Pre-shipment inspection and testing
  • Operator training and protocol guidance
  • One-year main-unit warranty
  • Six-month handpiece warranty where specified
  • 24/7 technical support
  • Applicator, consumable, and spare-parts support

Vaginal and Vulvar RF System FAQs

What is the difference between FeminaRF and RevivaV?
FeminaRF is configured for regulated internal vaginal and external vulvar RF applications. RevivaV is an external vulvar RF system only and does not include an internal vaginal applicator.
Can the RevivaV applicator be used internally?
No. RevivaV is an external-only system. Its applicator must not be inserted into the vaginal canal or promoted for internal vaginal treatment.
Does FeminaRF include HIFU?
The confirmed specification provided here identifies FeminaRF as a 5 MHz, 180W RF system. HIFU should not appear in the title or description unless a separate HIFU generator, handpiece, cartridges, and supporting documentation are actually included.
Are intimate RF procedures non-invasive?
They are generally non-surgical, but an internal vaginal applicator is intracavitary. Calling every procedure simply “non-invasive” may understate its medical, hygiene, and operator requirements.
Does vaginal RF strengthen pelvic floor muscles?
RF primarily produces controlled tissue heating. It does not directly generate repeated pelvic floor muscle contractions like EMS or electromagnetic pelvic-floor systems.
Can these machines treat urinary incontinence?
This is a regulated medical claim and should not be made unless the exact machine is authorized for that indication. Clients with urinary symptoms require appropriate clinical assessment.
Can intimate RF treat dryness or menopause symptoms?
These outcomes should not be guaranteed. Vaginal dryness and menopause-related symptoms can have multiple causes, and energy-based treatment claims require model-specific evidence and authorization.
Are the treatment tips reusable?
This depends on the exact component. Confirm whether each tip or cover is single-use, reusable after validated high-level disinfection, or sterilizable. Never reuse a single-use component.
Is treatment pain-free and risk-free?
No. Clients may experience heat or discomfort, and potential adverse effects can include burns, pain, scarring, infection, altered sensation, painful intercourse, and persistent symptoms.
What should I confirm before ordering?
Confirm the application area, RF frequency, output, electrode configuration, internal and external applicators, temperature monitoring, cooling, tips, hygiene validation, intended use, regulatory documentation, training, and warranty.

Compare Professional Intimate RF Systems

Tell Mico Aes whether you require internal and external capability or an external-only system, together with your provider type, destination country, voltage, consumable requirements, and documentation needs. Request Intimate RF System Information
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