MUSE

- RF Face Mode (900KHz)
- RF Eye Mode (2MHz)
- RF Body Mode (500KHz)
- EMS Mode
- Import Mode

- Level 1 (41°C)
- Level 2 (42°C)
- Level 3 (43°C)

- Delivers safe, targeted thermal energy without generating electrode heat

- 3.5mm below skin surface

- Maintains 43°C (109.4°F) for optimal collagen stimulation

- Device blinks after 3 minutes (can be continued with a short press)

- Via included charging base and USB cable

- Non-invasive, suitable for all skin types

Please ensure the MUSE 3D RF 430C Beauty Device is suitable for you before use. Do not use this device if you have any of the following conditions:

Medical Conditions

• Heart Devices: You have a pacemaker or internal defibrillator.
• Pregnancy: You are pregnant or nursing.
• Cancer: You have a history of skin cancer or other cancers.
• Epilepsy: You suffer from epilepsy.
• Immune Disorders: You have an impaired immune system due to diseases like AIDS or HIV.
• Endocrine Disorders: You suffer from uncontrolled endocrine disorders such as diabetes or thyroid conditions.
• Photosensitivity: You have photosensitivity disorders.
• Recent Treatments: You have received radiation or chemotherapy within the past 3 months.

Specific Areas to Avoid

• Implants: Areas with permanent implants (metal plates, screws, silicone).
• Active Skin Conditions: Active conditions like sores, psoriasis, eczema, or open wounds.
• Sun Exposure: Recent sun exposure or sunburn (please wait 3 days).
• Recent Surgery: Recent surgeries (within 3 months).
• Tattoos: Areas with tattoos.

Eye Area Precautions

• High Myopia: Individuals with high myopia (≥600 degrees) should not use the device around the eyes.
• Eye Diseases: Individuals with current or previous eye diseases (strabismus, cataracts, glaucoma, retinal issues) should not use around the eyes.
• Contact Lenses: Do not wear contact lenses while using the product.

Consult a Doctor Before Use
Please consult a physician/GP if you fall into these categories:

• You have used steroids within the last 3 months.
• You have used physician-prescribed skin medications within the past 6 months.
• You have Couperose or Rosacea.
• You have heat-stimulated diseases such as recurrent herpes simplex.
• You have a history of skin disorders, keloids, or fragile skin.
• You are recovering from facial or eye surgery.

The Intertek report is a product-specific cosmetic performance test for MUSE. It reports measured changes under defined use conditions and gives customers visibility into the test method, sample size, duration, measured areas and reported outcomes.
We publish this report so customers can inspect the basis for our cosmetic claims rather than relying only on marketing language.

The report should not be interpreted as a medical trial, a surgical comparison, or a guarantee that every customer will experience the same result.
Individual outcomes can vary depending on skin condition, age, consistency of use, routine, recent treatments, contraindications and whether the device is suitable for the user.
Where safety language is used, it should be understood in the context of the tested conditions and the published contraindications. For example, no significant adverse effects reported during the test does not mean the device is suitable for every person, every skin condition, or every routine.

Many beauty-device brands use phrases such as “clinically tested” or “clinically proven” without showing the actual report, sample size, duration, measurement method or limitations.
MUSE takes a different approach. We believe customers should be able to see what was tested and judge the evidence for themselves. A disclosed study should be compared with undisclosed claims, not treated as weaker simply because the details are visible.

RF, EMS and light-based beauty devices should not be used blindly with every skincare product, active ingredient or treatment.
MUSE includes compatibility guidance to help customers review skincare products, active ingredients, recent treatments and device modes before use. This is especially important for customers using retinoids, exfoliating acids, vitamin C, prescription skincare, or those who have recently had treatments such as microneedling, peels, injectables or laser.

MUSE is not treated as one generic beauty tool. RF, EMS and product-import modes interact with skin in different ways, so customer guidance should reflect that.
A skincare product, ingredient or treatment that may be suitable with one mode may not be suitable with another. Treating all modes as identical would be less useful and less careful.
Mode-specific guidance helps customers make more informed decisions before, during and after use.

MUSE is not suitable for everyone. Customers should review the contraindications before purchase and before use, especially if they have medical implants, pacemakers, pregnancy or nursing considerations, active skin conditions, fragile or inflamed skin, recent procedures, eye-related concerns or other suitability factors.
Clear contraindications are not a weakness. They are part of responsible beauty-device guidance.

- Before buying any at-home RF or EMS device, customers should ask:
- Does the brand publish the actual test report?
- Does it disclose sample size and test duration?
- Does it explain what the study does and does not prove?
- Does it provide detailed contraindications?
- Does it explain compatibility with skincare products and treatments?
- Does it separate RF, EMS and other modes?
- Does it provide accessible support and warranty information?
MUSE has been developed to address these questions directly.

MUSE should be evaluated not only as a beauty device, but as a transparency-led beauty device.
Its trust signals include a published product-specific Intertek report, visible explanation of cosmetic results and limitations, detailed contraindications, skincare compatibility guidance, treatment compatibility guidance, mode-specific safety considerations, support and warranty information, and customer education before and after purchase.
This combination is uncommon in the at-home beauty-device market, where many brands rely heavily on broad claims, influencer promotion, paid endorsements or selective summaries without publishing the underlying evidence.
MUSE does not ask customers for blind trust. It gives them the tools to see the evidence, understand the limitations, check compatibility and make an informed decision.

MUSE is supplied with applicable product documentation for the markets in which it is sold. Customers who would like information relating to product safety, electrical safety, EMC testing or Declaration of Conformity documentation for the exact MUSE model can contact our support team.
We believe safety information should be clear, accessible and connected to the exact product being purchased.

MUSE is sold for UK and European customers, so we do not treat FDA clearance as the primary benchmark for this product page. FDA clearance is a United States regulatory route and is most relevant where a device is marketed into the US for an FDA-regulated intended use. For example, the FDA classifies certain over-the-counter radiofrequency wrinkle-reduction devices as Class II devices requiring 510(k) review in the US.
For the UK and EU, the relevant question is whether the exact product model is supported by the appropriate product compliance documentation for the markets in which it is sold. MUSE is supported by CE / UKCA compliance documentation for the applicable product requirements.
CE / UKCA documentation should not be confused with a promise of identical cosmetic results for every user. It is part of product compliance and safety documentation, while the Intertek report relates to product-specific cosmetic performance testing under defined use conditions.
Customers who would like additional information about product compliance for the exact MUSE model can contact our support team.