CurrentBody Skin LED Mask Series 2
The CurrentBody Skin LED Mask Series 2 uses 236 LEDs at 633 nm, 830 nm, 1072 nm, in sessions of 10 min.
Brand-sponsored device studies. 633/830 nm are well studied; 1072 nm has thinner independent literature.
LED face masks · head to head
CurrentBody Skin LED Mask Series 2 vs
Dr. Renú SpectraLift™ Advanced
Two of the nine LED face masks in our comparison table, side by side. Every figure below is one the manufacturer publishes itself; where a brand stays silent the cell says so.
Side by side
The specifications
| Specification | CurrentBody Skin LED Mask Series 2 | Dr. Renú SpectraLift™ Advanced |
|---|---|---|
| Wavelengths | 633 nm830 nm1072 nm | 465 nm530 nm630–660 nm850 nm |
| LED count | 236 | 280 |
| Published irradiance | ~30 mW/cm² | Up to 50 mW/cm² |
| Session | 10 min | ~10 min |
| Modes | Single automatic programme | 9 selectable modes |
| Regulatory | FDA cleared · CE | FDA 510(k) K253712, Class II · CE · ISO 13485 · IEC 60601 · IEC 62471 |
| Fit | Flexible silicone | Flexible silicone, 300 g |
| Power | Rechargeable clip-on controller | Rechargeable 2000 mAh USB-C |
“Published irradiance” means the brand prints an output figure on its own product page. “FDA cleared” is not “FDA approved” — see the questions below.
Where they differ
- Wavelengths
- The CurrentBody Skin LED Mask Series 2 emits at 633 nm, 830 nm, 1072 nm. The Dr. Renú SpectraLift™ Advanced emits at 465 nm, 530 nm, 630–660 nm, 850 nm. Both cover red and near-infrared, the two ranges with the strongest published evidence for skin.
- LED count
- The Dr. Renú SpectraLift™ Advanced carries more diodes: 280 against 236. Diode count sets how evenly light reaches the face — a coverage figure, not an efficacy figure.
- Published irradiance
- Both publish an output figure: the CurrentBody Skin LED Mask Series 2 states ~30 mW/cm², the Dr. Renú SpectraLift™ Advanced states up to 50 mW/cm². Only three of the nine masks this site compares publish one at all.
- Regulatory
- The Dr. Renú SpectraLift™ Advanced prints a searchable 510(k) number (K253712); the CurrentBody Skin LED Mask Series 2 states its clearance without printing one. These devices are FDA cleared, not FDA approved — clearance is a safety and manufacturing signal, not proof of results.
- Session and modes
- The CurrentBody Skin LED Mask Series 2 runs 10 min per session (single automatic programme). The Dr. Renú SpectraLift™ Advanced runs ~10 min (9 selectable modes).
- Fit and power
- CurrentBody Skin LED Mask Series 2: flexible silicone; rechargeable clip-on controller. Dr. Renú SpectraLift™ Advanced: flexible silicone, 300 g; rechargeable 2000 mAh USB-C.
Evidence notes
What the specifications don’t tell you
Dr. Renú SpectraLift™ Advanced
The Dr. Renú SpectraLift™ Advanced uses 280 LEDs at 465 nm, 530 nm, 630–660 nm, 850 nm, in sessions of ~10 min.
Publishes an irradiance figure and states spectrometer testing. Its own efficacy testing is brand-run. The 465 nm blue and 530 nm green are less evidenced than the red and near-infrared.
Questions
Common questions
What is the main specification difference between the CurrentBody Skin LED Mask Series 2 and the Dr. Renú SpectraLift™ Advanced?
The CurrentBody Skin LED Mask Series 2 emits at 633 nm, 830 nm, 1072 nm. The Dr. Renú SpectraLift™ Advanced emits at 465 nm, 530 nm, 630–660 nm, 850 nm. Both cover red and near-infrared, the two ranges with the strongest published evidence for skin.
Both publish an output figure: the CurrentBody Skin LED Mask Series 2 states ~30 mW/cm², the Dr. Renú SpectraLift™ Advanced states up to 50 mW/cm². Only three of the nine masks this site compares publish one at all.
Which has more LEDs, the CurrentBody Skin LED Mask Series 2 or the Dr. Renú SpectraLift™ Advanced?
The Dr. Renú SpectraLift™ Advanced carries more diodes: 280 against 236. Diode count sets how evenly light reaches the face — a coverage figure, not an efficacy figure.
Are the CurrentBody Skin LED Mask Series 2 and the Dr. Renú SpectraLift™ Advanced FDA cleared?
CurrentBody Skin LED Mask Series 2: FDA cleared · CE. Dr. Renú SpectraLift™ Advanced: FDA 510(k) K253712, Class II · CE · ISO 13485 · IEC 60601 · IEC 62471. Clearance under section 510(k) means the manufacturer showed substantial equivalence to a device already on the market and met safety standards — it is not FDA approval, and it is not evidence of efficacy.