This Dermaplaning-Meets-Microneedling Treatment Is the Newest Way to Get Skin That Gleams and Glows
MIRApeel fuses two unique technologies—wet abrasion and wet microneedling—into a single treatment.
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Vivace Ultra Receives FDA Clearance
Aesthetics Biomedical’s Vivace Ultra microneedling RF device was cleared by the FDA for use in dermatological and surgical procedures.
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Emsculpt Neo Approved for Medical and Aesthetic Use
BTL’s Emsculpt Neo has received FDA clearance to stimulate neuromuscular tissue in the legs and arms for rehabilitation, expanding its original use for fat reduction and muscle building to now address medical conditions and improve patients’ mobility and recovery.
MedResults to Offer Benefits Related to ModMed to its Plastic Surgeons and Medical Spas
MedResults members may be eligible to receive offers related to ModMed’s integrated EHR, Practice Management, Patient Engagement and Inventory Management.
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AmSpa Announces Boot Camps and Courses Dates for 2022
The American Med Spa Association has announced the dates and locations for its seven Medical Spa & Aesthetic Boot Camps and 10 Academy for Injection Anatomy (AIA) courses for 2022.
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AmSpa Launches New Medical Spa State of the Industry Survey
The American Med Spa Association (AmSpa) announces that its new Medical Spa State of the Industry survey is open to medical spa professionals with results appearing in the 2022 Medical Spa State of the Industry Report.
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Crown Aesthetics Partners With Cosmetic Skin and Surgery Center Doctor
The partnership supports the development of medical education events focused on the benefits of ProGen PRP Advantage and SkinPenPrecision.
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FDA Clears Vivace RF Microneedling System at 2MHz Setting
Aesthetics Biomedical announces that the Vivace RF Microneedling device is now cleared for use at both the 1MHz and the 2MHz frequency.
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BENEV Launches Sylfirm X Ultimate Edition, a Novel Radiofrequency Microneedling Device
BENEV Company Inc launches a novel RF microneedling device, Sylfirm X, in the US as the exclusive distributor.
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Allegro Medspa Focuses on Female Health and Wellness
Dr Heather Furnas brings Cliovana (a non-invasive, patented treatment designed to improve women’s arousal levels, orgasm frequency and intensity) to Allegro Medspa.
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FDA Clears SkinPen Precision to Treat Neck Wrinkles
The U.S. Food and Drug Administration (FDA) has cleared the SkinPen Precision microneedling device to treat neck wrinkles. This means SkinPen is now cleared to treat both the face and neck, Crown Aesthetics announces.
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InMode Files ITC Complaint Against ILOODA and its US Distributor, Cutera
InMode Ltd has filed a complaint with the United States International Trade Commission alleging ILOODA’s SecretRF fractional radio frequency microneedling system, distributed in the United States by Cutera Inc, infringes U.S. Patent No. 10,799,285.
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Everything You Need to Know About Radiofrequency Microneedling for Acne Scars
After exhausting every topical “fading” treatment, it’s time to elevate your plan of attack, according to Women’s Health.
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All About Radiofrequency Microneedling
Compared with treatments like chemical peels and dermabrasion, radiofrequency microneedling is minimally invasive. Healthline shares more about the procedure, side effects, and benefits.
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The American Med Spa Association (AmSpa) Acquires the Academy for Injection Anatomy (AIA)
The American Med Spa Association (AmSpa) has acquired the Academy for Injection Anatomy (AIA), a clinical training program for injectors, it announces.
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Platelet-Rich Plasma’s Use in Plastic Surgery is Evolving in These Ways
The American Society of Plastic Surgeons reports a 25% increase in cosmetic platelet-rich plasma use in the last 4 years. A study in Plastic and Reconstructive Surgery takes a look at this evolution.
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The Absolute Best Dermarollers for DIY Treatments
In Shape, experts break down how to safely use a dermaroller and the best dermarollers you can buy
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FDA Finalizes Guidance on Microneedling Devices
The US Food and Drug Administration (FDA) [recently] finalized guidance explaining when it considers microneedling devices to be medical devices subject to premarket notification (510(k)) requirements, Regulatory Focus reports.
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