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Microfocused ultrasound: brows rose 0.47–1.7 mm, and 42% of patients said they saw a change

In a 2023 systematic review of 16 studies, brow lift measured **0.47–1.7 mm** and submental area fell **26–45 mm²**. In the same data, 92% were classed as improved by the treating physician — but **only 42% of patients said so themselves.** The gap between those two numbers is the honest size of this procedure.

Last checked Sep 17, 2026

Korean classification Being checkedThe regulatory class has not yet been confirmed against a primary document. It will be filled in once it is.

Microfocused ultrasound with visualisation (MFU-V) focuses ultrasound to a point beneath the skin, creating small coagulation zones. In Korea the best-known brand is Ulthera.

This is not a topical cosmetic. It is a device procedure performed in a clinic, and this layer is kept separate from the ingredient layer.

The regulatory situation is the same as for radiofrequency: we have not yet opened the Korean device approval record, so this page says 'being verified'.

What is established

Moderate evidence

Measured in millimetres, brows rise about 1 mm

The 2023 systematic review screened 693 studies and kept 16. The inclusion criteria took randomised trials, controlled trials, cohorts — and case series of 10 or more.

The objectively measured values: brow lift 0.47–1.7 mm, and a 26–45 mm² reduction in submental area on lateral photographs.

It matters to look at those numbers as they are. A millimetre or so is a real change, but it is not the size that advertising photographs imply. This is the honest scale of the procedure.

The limits are equally clear. Some of the 16 are uncontrolled case series, every included study was in women only, and device settings and energies varied between studies. The authors noted that results decline with greater laxity and with a BMI above 30.

  • Open-label trial in people (16) · sample size not reported · 52 weeks · Compared with no control group (before-and-after only) · Funding not declared · Endpoint instrument measurement PMID 36674277
Early research

Physicians said 92%; patients said 42%

The same review pooled two satisfaction scores separately.

Physician-rated (IGAIS, n = 337): 92% were classed as improved at day 90.

Patient-rated (SGAIS, n = 81): 42% at day 90, rising to 53% at day 360. The authors described the improvements as mild.

The same people, the same time point, and the scores split 92% against 42%. That does not mean one side is wrong. It means what you choose to measure can more than double the apparent size of the same procedure. This is exactly why this site shows the endpoint next to the evidence grade.

  • Open-label trial in people (16) · 81 participants · 52 weeks · Compared with no control group (before-and-after only) · Funding not declared · Endpoint self-reported improvement PMID 36674277
Not established

We found no trial with a sham control

The same problem as on the radiofrequency page. Every randomised trial we read used either a different setting of the same device or a different device as its control. None compared against doing nothing.

The 16 studies in the systematic review also include uncontrolled case series. A change measured against baseline cannot be separated from time, lighting, posture, or knowing you were treated.

The review's authors wrote that future work should focus on objective outcome measures — which is another way of saying that the evidence so far leans heavily on subjective assessment.

Early research

The arm and abdomen trials compared one setting of the device against another

The 2021 trial randomised 30 people with upper-arm laxity to a single depth on one arm and two depths on the other. The 2020 trial used the same structure on the abdomen in 30 people, of whom 28 finished.

In both, single-plane and dual-plane came out the same. Arm circumference fell modestly on both sides.

Look at the design again: both sides were treated. So the question these trials answered is 'are two depths better than one', not 'does microfocused ultrasound work'.

One detail in the abdominal trial stands out. Participants who had given birth scored significantly higher on both physician and patient ratings, and their waist reduction was significant too. The sample is too small to settle anything, but it is a signal that who is treated moves the result a great deal.

  • Randomised controlled trial in people · 30 participants · 26 weeks · Compared with another active ingredient · Funding not declared · Endpoint scores from blinded assessors PMID 32770693
  • Randomised controlled trial in people · 30 participants · 26 weeks · Compared with another active ingredient · Funding not declared · Endpoint scores from blinded assessors PMID 32173882

Known risks

  • Pain during treatment is common. The review called it moderately painful, and in the 2017 head-to-head against radiofrequency, the ultrasound side hurt more.
  • Transient erythema and swelling are common.
  • Other adverse effects in the review totalled 2%: dysaesthesia (numbness or hypersensitivity), bruising, stinging, mandibular burns, striations and contact dermatitis.
  • Marked laxity and a BMI above 30 were proposed as relative contraindications.
  • Any adverse reaction is something to have seen by the clinic that performed the procedure.

What is not established

  • We have not verified the Korean device approval class.
  • There is no follow-up data beyond one year; the review says so explicitly.
  • There is no data in men. All 16 included studies were in women.
  • Which device settings and energies are better — they varied between studies.
  • How it compares against doing nothing at all.

Whether to have it done is a decision to make with a doctor.

What this article relies on

  1. PubMed — 미국 국립의학도서관 문헌 데이터베이스National Library of Medicine · Checked on 2026-09-16