Bottom Line
The Booster Pro is a multi-modal device that integrates 630nm LED, an EMS mode marketed as microcurrent, electroporation, sonic vibration, and a warming/cooling mode we couldn't independently confirm. Its real strength is helping serums penetrate deeper into the skin. As an LED-only treatment, it's limited to one wavelength - but as a tool to maximize the skincare you're already buying, it's a strong choice.
Check current price on Amazon → (paid link)
Wavelength Breakdown
What It Does
- 630nm red LED for surface collagen support
- EMS/microcurrent for muscle stimulation
- Electroporation for enhanced product penetration
- Sonic vibration for circulation
- Warming and cooling modes we couldn’t independently confirm
- Light therapy + serum infusion combined
What We Liked
- Designed to boost product absorption via EMS/microcurrent and electroporation
- Compact and portable
- Useful even on days you don’t have time for a full mask session
- Strong build quality for the price tier
What We Didn’t Like
- Single LED wavelength - not a substitute for a multi-wavelength mask
- Treating the full face takes longer than a mask session
- Lots of features to learn; not as plug-and-play as a mask
Who It Suits
- Skincare enthusiasts who want to amplify their serums
- Owners of an LED mask who want a portable supplementary device
- People who like multi-function gadgets
Who Should Choose Something Else
- Primary anti-aging device → CurrentBody Series 2
- Best value mask → iRestore Illumina
FDA Registry Check
Our 510(k) and GUDID searches did not produce a record we could link to the Medicube Booster Pro by name. Four 510(k) searches - “Medicube” as both device name and applicant, “Booster Pro” as device name, “6-in-1” as device name - returned zero results. Two of four GUDID searches (“Medicube,” “AGE-R”) also returned zero; the other two (“Booster Pro,” “APR Factory”) returned 15,634 and 5,026 results respectively - generic full-text hits, not device matches.
What the search did find is in FDA Registration & Listing. A proprietary-name search for “Medicube” returned six results; four carry a device name matching this product. Three list “MEDICUBE AGE-R BOOSTER PRO” - registered under the applicant name APR Co., Ltd. (registration number 3016769192) and, separately, APR FACTORY Co.,Ltd (3030186811 and 3031232522) - and a fourth lists “MEDICUBE AGE-R BOOSTER PRO PINK,” under APRFACTORY (3031570300): three different renderings of the applicant name across the four listings. None of the four carries a 510(k) number, product code, or decision date. Listed in FDA Registration & Listing as Massager, Therapeutic, Electric - a different regulatory category from the over-the-counter light-based devices this catalog otherwise checks. Checked Aug 14, 2026; see our full clearance check for all nine searches run and what each returned.
🔧 Verdict
A clever multi-tool, not a primary anti-aging LED device. Buy it as a companion to your mask, or if you're more focused on optimizing your serum routine than on light therapy itself.
Check Current Price on Amazon → (paid link)
Frequently Asked Questions
Is the Medicube Booster Pro FDA-cleared?
We searched FDA's 510(k) and GUDID databases directly for "Medicube," "Booster Pro," "AGE-R," and "6-in-1"; none returned a record. What we found instead is four FDA Registration & Listing entries under variations of the device's own name, classified as Massager, Therapeutic, Electric - not the over-the-counter light-based category this catalog otherwise checks. See our full clearance check for exactly what each search returned.
What does 'Massager, Therapeutic, Electric' mean for this device?
It's the device category FDA's Registration & Listing database associates with this device's own listings - a different regulatory category from the over-the-counter light-based devices (LED masks) this catalog otherwise checks. We're reporting the listed category, not interpreting what it implies about safety or effectiveness.
Who is the manufacturer, according to the FDA registration records?
Four FDA Registration & Listing entries exist under device names matching this product. Their applicant field is rendered three different ways across those entries: APR Co., Ltd. (registration number 3016769192), APR FACTORY Co.,Ltd (3030186811 and 3031232522), and APRFACTORY (3031570300, on the "PINK" listing). We're showing all three as recorded, not picking one as canonical.
Does the Medicube Booster Pro have a 510(k) clearance number?
Our direct 510(k) database searches (device name and applicant, four terms total) returned zero results, and none of the four Registration & Listing entries we found for this device carries a 510(k) number.
Where can I see every FDA registry search run for the Medicube Booster Pro?
In our full clearance check, which lists every search across all 13 devices in this catalog, including the nine run for this one.