logo
Sofwave: The Latest Non-Invasive Treatment Kissed By The Kardashians

Sofwave: The Latest Non-Invasive Treatment Kissed By The Kardashians

Forbes04-04-2025

Sofwave
When it comes to staving off the physical effects of aging, I am in the camp that I will eventually have a face lift, which at my age could be a few years away. However, until then I am always on the lookout for non-invasive aesthetic treatments (typically energy-based) that delay the need for me to go under the knife. One of the trendiest non-invasive treatments made a household name by the Kardashians is Sofwave, a skin tightening treatment that utilizes ultrasound to lift the skin on the face and body.
While I haven't had this treatment, which has been around since 2016 yet, with all the buzz it's been garnering I wanted to learn more about it from the people who make the device, those who use it in their aesthetic practices, and those who are familiar with Sofwave's technology but use something akin to it in their practice. Equally as important, I wanted to see if the 'Kardashian effect' (a term dubbed for the uptick in an aesthetic procedure after they tout it on their social channels) converts to real clients for aesthetic business owners.
What Is Sofwave?
James Bartholomeusz, Chief Innovation Officer for Sofwave explains to me over email that what makes their technology unique is that unlike other skin-lifting technologies such as micro-focused (MFU) or high-intensity focused ultrasound (HIFU) devices, Sofwave, a trademarked name, utilizes a proprietary high-frequency, non-focused ultrasound technology known as SUPERB (Synchronous Ultrasound Parallel Beam).
'SUPERB™ delivers energy precisely into the mid-dermis—bypassing deeper structures like nerves and fat—which maximizes safety and eliminates unnecessary tissue damage,' continues Bartholomeusz. 'Most importantly, this focused delivery stimulates the volumetric production of collagen and elastin, the key building blocks for skin firmness and elasticity.' The results, he shares are a 'a powerful regeneration response in the area of highest fibroblast activity, producing natural-looking, consistent results.'
Currently, Sofwave has 7 FDA clearances including lifting the eyebrows, neck, and submental. improving facial lines and wrinkles, lifting lax skin on the upper arms, improving the appearance of cellulite, and treating acne scars.
'Our newest clearance for arm laxity treatments has been a huge hit, especially with GLP 1 patients,' shares Bartholomeusz. Results are typically seen after one treatment. Although Bartholomeusz adds that in some instances a second treatment may be necessary depending on the desired results depending on the age, skin conditions, and treatment goals of the patient. 'Clinical studies and FDA clearance support that results can last up to 12 months or more following a single treatment. As the skin continues to remodel over time, patients experience progressive improvements in skin firmness, texture, and lift, with a natural-looking outcome and high patient satisfaction.'
Skinney Medspa 30 E 60 ground floor New York, NY 10022
'Sofwave is one of our top three requested services,' shares Adriana Martino, co-founder of Skinney Medspa, a multi-location aesthetic practice she founded alongside of her twin sister Marisa Martino—both of which are licensed estheticians who provide treatments. 'We were one of the first adopters of the technology. So many companies come to us with their devices. If we don't love it, we say no thank you to the company. With Sofwave, as soon as we saw the results, we knew we wanted it for our practices.'
What kind of results can be expected?
To date, Skinney Medspa has performed Softwave 240 treatments since they started offering the treatment back about a year ago 'It is great for post baby skin sagging,' Martino tells me on a call. 'We like to do Morpheus8 for crepey skin followed by Sofwave, which goes deeper into the skin.' The practice also performs the treatment regularly on the stomach and the back of the arms, also known as bat wings. 'The neck is also a highly requested treatment area in addition to what we call a non-invasive brow lift that helps lift tired, sagging eyes look more youthful.'
Leading Beverly Hills-based plastic surgeon Dr. Paul Nassif, MD, FACS tells me over email that he uses Sofwave in his practice because the non-invasive ultrasound treatment naturally stimulates collagen, elastin, and hyaluronic acid. 'We use it to improve fine lines and wrinkles, and to lift the eyebrows, submental (chin), and neck areas. It's also FDA-cleared for the short-term improvement of cellulite, to treat acne scars, and improve skin laxity on the upper arms. You might say it's a multi-tasking treatment device.'
Sofwave Results
As for results, Nassif explains to me that many of his patients are seeing results even after one 30–45-minute treatment with results continuing to improve for up to 12 weeks. Nassif does note that some patients may need another treatment to achieve their desired results and then can switch to annual maintenance.
'It's an excellent option for patients who aren't quite ready to do something more invasive, and I love that it integrates seamlessly with both surgical and non-surgical treatments. I often pair it with my Nassif MD clinical skincare line. Think of it as the perfect complement to a facelift—an ideal annual tune-up to help maintain a refreshed, youthful look. Patients love it because there is no lost-time after treatment, and they can immediately resume daily activities without anyone knowing they had an in-office treatment.'
How does Sofwave differ from Ultherapy?
With other skin tightening ultrasound-based technologies on the market, I wanted to get another perspective on how Sofwave differs from other ultrasound technologies. I reached out New York City-based Dr. Jennifer Levine, a double-board certified plastic surgeon who is familiar with Sofwave's technology but has been using Ultherapy for almost ten years and has performed roughly 1000 treatments with the device.
Sofwave Results
'Both technologies utilize ultrasound technology that causes a thermocoagulation point that stimulates the body to naturally produce collagen and elastin in the treatment area,' Levine tells me over a call. 'What I like about Ultherapy is that the device allows the practitioner to visualize the tissue being treated and at customizable depths. Sofwave treats the skin at a depth of 1.5mm, whereas with Ultherapy you can treat areas such as the superficial musculoaponeurotic system (this area located in the cheek region of the face plays an important role and facial expression, overall structure in the shape of the face, and provides a framework for the skin) at 3-4mm in depth, which is why Ultherapy utilizes visualization technology—so the practitioner can see what they are doing.'
In the end, Levine tells me that both devices work. But if your skin needs deeper skin tightening in certain areas, then Ultherapy may yield better results.
Is the Kardashian Effect Real?
When I ask if the 'Kardashian Effect' has provided a boost in Nassif's business he responds, 'We haven't seen an uptick yet, but I imagine the Kardashian effect will be incredibly impactful in driving brand awareness and elevating visibility among a wider digital audience.' In contrast, Martino tells me that Kim Kardashian raving about this treatment has increased sales dramatically. She tells me, 'Year-to date sales have increased by %70 when average sales grow typically %20 annually. We can attribute the increase in demand to the Kardashian's popularity.'
This is definitely an aesthetic treatment that's on my radar. And like many other people, I can thank the Kardashians for placing it there.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

These Popular Eggs Are Being Recalled Over Salmonella Risk
These Popular Eggs Are Being Recalled Over Salmonella Risk

Yahoo

time37 minutes ago

  • Yahoo

These Popular Eggs Are Being Recalled Over Salmonella Risk

If you've been living for your morning sunny-side eggs…well, brace yourself. The August Egg Company—the parent behind Sunnyside, Clover, Raley's, and a few other brands—is recalling a whopping 1.7 million dozen eggs due to a potential salmonella outbreak. Yep, it's serious.. The U.S. Food and Drug Administration (FDA) and Centers for Disease Control and Prevention have flagged the August Company's 'brown cage-free and brown certified organic egg' for possible contamination, meaning you might want to double-check that carton in your fridge before cracking it open. If you didn't know, Salmonella is that sneaky bacteria behind food poisoning and can cause anything from mild stomach upset to serious illness. These eggs were shipped to Walmart stores and other grocers in nine states: California, Washington, Nevada, Arizona, Wyoming, New Mexico, Nebraska, Indiana, and Illinois. They have a best-by date from March 4 to June 19 and food codes P-6562 or CA5330. Not sure if your eggs are on the list? The FDA has a full rundown of all the recalled brands you can check out. And if the cartons in your fridge match any of the food codes or best-by-dates, toss them out immediately. While it's somewhat okay to eat an egg past its expiration date, this isn't the case. The FDA has already connected a current salmonella outbreak to the eggs. As of now, a total of 79 cases have been reported in seven states, while 21 people have been hospitalized. We get it: eggs are pricey, and tossing them feels like a waste. But don't risk it. Plus, most places will give you a full refund. And if your eggs touched any surfaces, wipe those down like your life depends on it. If after eating you feel dizzy, nauseous, or get a fever—don't play it cool. Call your doctor. This is serious business. Trust me, as a four-time survivor of food poisoning, you don't want to take any chances. You Might Also Like Insanely Easy Weeknight Dinners To Try This Week 29 Insanely Delicious Vodka Cocktails

AG pushes back on federal abortion medication restrictions
AG pushes back on federal abortion medication restrictions

Yahoo

time3 hours ago

  • Yahoo

AG pushes back on federal abortion medication restrictions

BOSTON (SHNS) – Attorney General Andrea Campbell implored federal regulators Thursday to eliminate medication abortion restrictions on prescribers and pharmacies, arguing Massachusetts already has 'robust' guardrails in place to protect patient safety. Campbell, along with AGs from California, New York and New Jersey, want the U.S. Food and Drug Administration to eliminate its Risk Evaluation and Mitigation Strategy (REMS) program for mifepristone — or at least stop applying certain parts of it to the four petitioning states. The program outlines certification requirements for health care providers and pharmacies to dispense mifepristone, plus paperwork that patients must sign. About 65% of abortions in Massachusetts in 2023 were medication abortions, according to the 64-page citizen petition Campbell co-filed Thursday. The FDA says REMS programs are used for drugs with 'serious safety concerns to help ensure the benefits of the medication outweigh its risks.' Campbell's office contends the mifepristone requirements impose 'burdensome restrictions on access to medication abortion while not meaningfully improving patient safety, and that these restrictions severely impede patient access by reducing the number of prescribers and pharmacies authorized to dispense this FDA-approved medication.' 'The Mifepristone REMS Program also imposes an undue burden on pregnant patients experiencing miscarriage and early pregnancy loss who seek treatment at emergency departments,' the petition says. 'For instance, the administrative requirements imposed by the REMS can effectively discourage emergency departments from carrying mifepristone in their pharmacies.' Reduced access to mifepristone can particularly impact patients in rural and medically underserved areas, the petition added. The Democratic AGs teamed up in response to U.S. Health and Human Services Secretary Robert Kennedy recently instructing FDA Commissioner Martin Makary to pursue a 'complete review' of mifepristone and labeling requirements. The FDA is required to respond to their petition within 180 days by either approving, denying or dismissing it — or providing a 'tentative response' about why the agency is unable to reach a decision yet, according to federal regulations. In response to the Trump administration, Beacon Hill lawmakers are escalating their focus on shoring up protections for reproductive and transgender care. A Sen. Cindy Friedman bill (S 2522) that's gaining traction would tighten the 2022 abortion shield law, including by requiring hospitals to provide emergency abortion care and allowing provider practices, rather than specific prescriber names, to appear on medication abortion labels. WWLP-22News, an NBC affiliate, began broadcasting in March 1953 to provide local news, network, syndicated, and local programming to western Massachusetts. Watch the 22News Digital Edition weekdays at 4 p.m. on Copyright 2025 Nexstar Media, Inc. All rights reserved. This material may not be published, broadcast, rewritten, or redistributed.

Baby swabs and nasal swabs recalled for possible fungus in swab parts
Baby swabs and nasal swabs recalled for possible fungus in swab parts

Miami Herald

time6 hours ago

  • Miami Herald

Baby swabs and nasal swabs recalled for possible fungus in swab parts

Swabs for teething babies and adult noses have been recalled because they might have a microbial contamination 'identified as fungi in cotton swab components.' That's what manufacturer Church & Dwight said in its notice announcing the recall of Orajel Baby Teething Swabs, Zicam Cold Remedy Nasal Swabs and Zicam Nasal AllClear Swabs from stores across the United States, including Puerto Rico. The lots and expiration dates involved? All. READ MORE: Recalled UTI drug could have deadly microbial contamination What can contaminated swabs do? Swabs with a microbial contamination can cause 'serious and life-threatening blood infections in users whose nasal mucosa may be compromised due to inflammation and mechanical injurie,' the recall notice states. 'The risk is highest (potentially severe or life-threatening) among children and individuals with compromised immune systems or other underlying medical conditions.' Exactly which Orajel and Zicam swabs are recalled? ▪ Zicam Cold Remedy Nasal Swabs carry UPC No. 732216301205. ▪ Zicam Nasal AllClear Swabs, which were discontinued in December, carry UPC No. 732216301656. ▪ Orajel baby swabs carry UPC No. 310310400002. What should you do now? If you have the swabs, throw them in the trash or, for a refund, reach out go Church & Dwight either online or by calling 800-981-4710. Questions can be directed to that phone number, 9 a.m. to 5 p.m., Monday through Friday. If you think you or your baby is having a medical issue caused by these swabs, go see a medical professional. Then, notify the FDA's MedWatch Adverse Event Program, either by filling out a form online or by requesting a reporting form at 800-332-1088. Then, third, call Church & Dwight.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store