Tighten & Smooth

Say goodbye to puckered, dimpled skin with Emtone, a non-invasive treatment that smooths out cellulite and improves the skin’s overall texture. Emtone is ideal for those seeking to reduce stubborn cellulite after all other methods have failed, including traditional diet and exercise. Emtone is also non-invasive and cleared by the FDA when used in cellulite reduction and to improve overall skin tone, so you know you’re getting a safe, effective treatment that will leave your skin looking and feeling healthier.

Emtone works by using a combination of heat via radiofrequency (RF) energy and targeted pressure to hit the primary sources of cellulite. What you’re left with is a boost in new collagen and improved elastin, two key components that will give you the dimple-free skin that can be so elusive. Rock those shorts, smooth your tummy and enhance the skin’s laxity in any areas suffering from cellulite.

Take that next step to smooth and tighten your skin with Emtone in Orange County. Our experts at the Med Lounge can help you come up with an individualized cellulite treatment plan that will get your skin on its way to its new, dimple-free existence. Love the skin you’re in again with Emtone.


Smooth and tighten

Non-invasive treatment

Reduce cellulite

Improve skin laxity

Boost collagen production

Zero downtime

Confidence boost

Painless and effective

Works for all skin types

Extremely safe

Frequently Asked Questions

Emtone is a non-invasive treatment that uses a device that simultaneously delivers both thermal and mechanical energy to go after the main factors behind cellulite. That combination treatment is more effective than any one method alone, leading to more long-lasting, desirable results in patients dealing with cellulite.

Yes, Emtone reduces cellulite. It does so by heading off the main reasons why cellulite happens in the first place: reduced skin elasticity, enlarged fat chambers under the skin, poor blood flow, waste and water retention, and rigid fibers beneath the skin that cause that tell-tale dimpling.

Repeated treatments as part of an individualized Emtone treatment plan lead to not only an overall reduction of cellulite over time but improved skin laxity and texture within weeks of your treatments.

Emtone works by combining dual technologies (thermal and mechanical energy) to target the causes of cellulite. Thermal energy comes in radiofrequency (RF) energy, heating the skin to tighten the skin’s fibers and boost collagen production. 

Mechanical energy in the form of acoustic energy penetrates the skin, boosting circulation and reducing waste and fluid retention that is another culprit behind cellulite.

Both processes disrupt the fat chambers and rigid skin fibers, creating those uneven, dimpled surfaces in the upper layers of the skin. Emtone uses your skin’s natural processes to stimulate a response that supports new collagen and elasticity, dramatically improving the appearance of cellulite in targeted areas.

Treatments typically take about 20 minutes from start to finish. Most patients will benefit from four of these 20-minute treatments over 2-4 weeks, but your provider will develop a treatment plan with you based on your goals. How many treatments you include as part of your plan will determine your Emtone cost so pricing will vary by individualized treatment plan.

Emtone doesn’t hurt. Some patients even compare it to a hot stone massage with mechanical vibrations as your provider applies the device to your skin. The heating effect comes from the radiofrequency energy used as part of the treatment. At the same time, your provider uses targeted pressure energy to boost circulation in your treatment zones. All of this happens while you’re lying down and relaxing for the 20 minutes or so your treatment will take.

There’s no downtime after your treatment, so you’ll be able to get back to your day-to-day activities right after your therapy.

Your Emtone results will last anywhere from three months to a year. While some will see improvements to their cellulite after just one session, don’t expect final results until about three months after your last session. The wait is worth it!

Touchup treatment sessions are recommended to maintain those skin-smoothing results. How often you come in for a touchup will depend on your body. Some come in annually to see the results they crave, while others will need more frequent visits to maintain results.

See the amazing difference in our clients, before and after treatment.

Click the image to see an enlarged preview.

What to Expect With Emtone

For the best results and to reduce the chance of any side effects after your treatment, our experts at the Med Lounge have a few tips around what to expect with Emtone before and after your procedure.


  • Wear comfortable clothing on the day of your treatment. Your provider will need easy access to areas being targeted during your procedure.
  • Leave the skin free of any lotions, makeup or serums the day of your treatment. 
  • Remove any jewelry and put away electronic devices before starting your treatment. 
  • Hydration is important. Come to your appointment well-hydrated, and drink plenty of water in the days leading up to your treatment. Avoid beverages with a diuretic effect, like drinks containing caffeine and alcohol, in a day or two ahead of your treatment.
  • Talk to your provider about any cardiovascular conditions, implants or injuries you’ve experienced in the areas you’d like to target. Your provider will be able to tell you whether Emtone is safe for you or whether you’re a better candidate for a different kind of treatment that will get you the results you’re looking for.


  • You shouldn’t expect any downtime after treatment and should be able to return to your regular, daily activities right after your treatment. 
  • You may experience some soreness in the treated area in the days post-treatment. This is normal and will go away on its own within a day or so.
  • Any redness you see on your skin after your treatment is temporary and should go away the same day of your Emtone procedure. This is a result of the heating effects of your Emtone treatment.
  • Keep well-hydrated in the days after treatment. Hydration boosts elasticity in the skin, improves tone, and helps you feel your best after your procedure.
  • The recommended minimum number of sessions for optimal results is four sessions. Some patients will benefit from six total sessions, depending on the treatment areas targeted. Schedule your sessions as recommended by your provider at the end of your Emtone appointment, and follow treatment instructions to the letter.

Emtone™ is intended to provide heating for the purpose of elevating tissue temperature for selected medical conditions such as temporary relief of pain, muscle spasms, and increase in local circulation. EMTONE massage device is intended to provide a temporary reduction in the appearance of cellulite.

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BOTOX® Cosmetic (onabotulinumtoxinA) Important Information



BOTOX® Cosmetic (onabotulinumtoxinA) is indicated in adult patients for the temporary improvement in the appearance of:

– Moderate to severe glabellar lines associated with corrugator and/or procerus muscle activity

– Moderate to severe lateral canthal lines associated with orbicularis oculi activity


– Moderate to severe forehead lines associated with frontalis activity





Postmarketing reports indicate that the effects of BOTOX® Cosmetic and all botulinum toxin products may spread from the area of injection to produce symptoms consistent with botulinum toxin effects. These may include asthenia, generalized muscle weakness, diplopia, ptosis, dysphagia, dysphonia, dysarthria, urinary incontinence, and breathing difficulties. These symptoms have been reported hours to weeks after injection. Swallowing and breathing difficulties can be life threatening and there have been reports of death. The risk of symptoms is probably greatest in children treated for spasticity, but symptoms can also occur in adults treated for spasticity and other conditions, particularly in those patients who have an underlying condition that would predispose them to these symptoms. In unapproved uses and approved indications, cases of spread of effect have been reported at doses comparable to those used to treat cervical dystonia and spasticity and at lower doses.


BOTOX® Cosmetic is contraindicated in the presence of infection at the proposed injection site(s) and in individuals with known hypersensitivity to any botulinum toxin preparation or to any of the components in the formulation.


Lack of Interchangeability Between Botulinum Toxin Products

The potency units of BOTOX® Cosmetic are specific to the preparation and assay method utilized. They are not interchangeable with other preparations of botulinum toxin products and, therefore, units of biological activity of BOTOX® Cosmetic cannot be compared to nor converted into units of any other botulinum toxin products assessed with any other specific assay method.

Spread of Toxin Effect

Please refer to Boxed Warning for Distant Spread of Toxin Effect.

No definitive serious adverse event reports of distant spread of toxin effect associated with dermatologic use of BOTOX® Cosmetic at the labeled dose of 20 Units (for glabellar lines), 24 Units (for lateral canthal lines), 40 Units (for forehead lines with glabellar lines), 44 Units (for simultaneous treatment of lateral canthal lines and glabellar lines), and 64 Units (for simultaneous treatment of lateral canthal lines, glabellar lines, and forehead lines) have been reported. Patients or caregivers should be advised to seek immediate medical care if swallowing, speech, or respiratory disorders occur.

Serious Adverse Reactions With Unapproved Use

Serious adverse reactions, including excessive weakness, dysphagia, and aspiration pneumonia, with some adverse reactions associated with fatal outcomes, have been reported in patients who received BOTOX® injections for unapproved uses. In these cases, the adverse reactions were not necessarily related to distant spread of toxin, but may have resulted from the administration of BOTOX® to the site of injection and/or adjacent structures. In several of the cases, patients had pre-existing dysphagia or other significant disabilities. There is insufficient information to identify factors associated with an increased risk for adverse reactions associated with the unapproved uses of BOTOX®. The safety and effectiveness of BOTOX® for unapproved uses have not been established.

Hypersensitivity Reactions

Serious and/or immediate hypersensitivity reactions have been reported. These reactions include anaphylaxis, serum sickness, urticaria, soft-tissue edema, and dyspnea. If such reactions occur, further injection of BOTOX® Cosmetic should be discontinued and appropriate medical therapy immediately instituted. One fatal case of anaphylaxis has been reported in which lidocaine was used as the diluent and, consequently, the causal agent cannot be reliably determined.

Cardiovascular System

There have been reports following administration of BOTOX® of adverse events involving the cardiovascular system, including arrhythmia and myocardial infarction, some with fatal outcomes. Some of these patients had risk factors including pre-existing cardiovascular disease. Use caution when administering to patients with pre-existing cardiovascular disease.

Increased Risk of Clinically Significant Effects With Pre-existing Neuromuscular Disorders

Individuals with peripheral motor neuropathic diseases, amyotrophic lateral sclerosis, or neuromuscular junction disorders (eg, myasthenia gravis or Lambert-Eaton syndrome) should be monitored when given botulinum toxin. Patients with neuromuscular disorders may be at increased risk of clinically significant effects including generalized muscle weakness, diplopia, ptosis, dysphonia, dysarthria, severe dysphagia, and respiratory compromise from onabotulinumtoxinA (see Warnings and Precautions).

Dysphagia and Breathing Difficulties

Treatment with BOTOX® and other botulinum toxin products can result in swallowing or breathing difficulties. Patients with pre-existing swallowing or breathing difficulties may be more susceptible to these complications. In most cases, this is a consequence of weakening of muscles in the area of injection that are involved in breathing or oropharyngeal muscles that control swallowing or breathing (see Boxed Warning).

Pre-existing Conditions at the Injection Site

Caution should be used when BOTOX® Cosmetic treatment is used in the presence of inflammation at the proposed injection site(s) or when excessive weakness or atrophy is present in the target muscle(s).

Dry Eye in Patients Treated With BOTOX® Cosmetic

There have been reports of dry eye associated with BOTOX® Cosmetic injection in or near the orbicularis oculi muscle. If symptoms of dry eye (eg, eye irritation, photophobia, or visual changes) persist, consider referring patients to an ophthalmologist.

Human Albumin and Transmission of Viral Diseases

This product contains albumin, a derivative of human blood. Based on effective donor screening and product manufacturing processes, it carries an extremely remote risk for transmission of viral diseases and variant Creutzfeldt-Jakob disease (vCJD). There is a theoretical risk for transmission of Creutzfeldt-Jakob disease (CJD), but if that risk actually exists, the risk of transmission would also be considered extremely remote. No cases of transmission of viral diseases, CJD or vCJD have ever been identified for licensed albumin or albumin contained in other licensed products.


The most frequently reported adverse reactions following injection of BOTOX® Cosmetic for glabellar lines were eyelid ptosis (3%), facial pain (1%), facial paresis (1%), and muscular weakness (1%).

The most frequently reported adverse reaction following injection of BOTOX® Cosmetic for lateral canthal lines was eyelid edema (1%).

The most frequently reported adverse reactions following injection of BOTOX® Cosmetic for forehead lines with glabellar lines were headache (9%), brow ptosis (2%), and eyelid ptosis (2%).


Co-administration of BOTOX® Cosmetic and aminoglycosides or other agents interfering with neuromuscular transmission (eg, curare-like compounds) should only be performed with caution as the effect of the toxin may be potentiated. Use of anticholinergic drugs after administration of BOTOX® Cosmetic may potentiate systemic anticholinergic effects.

The effect of administering different botulinum neurotoxin products at the same time or within several months of each other is unknown. Excessive neuromuscular weakness may be exacerbated by

administration of another botulinum toxin prior to the resolution of the effects of a previously administered botulinum toxin.

Excessive weakness may also be exaggerated by administration of a muscle relaxant before or after administration of BOTOX® Cosmetic.


There are no studies or adequate data from postmarketing surveillance on the developmental risk associated with use of BOTOX® Cosmetic in pregnant women. There are no data on the presence of BOTOX® Cosmetic in human or animal milk, the effects on the breastfed child, or the effects on milk production.


Please see BOTOX® Cosmetic full Prescribing Information including Boxed Warning and Medication Guide.