LED face masks · head to head

Omnilux Contour Face vs
Shark CryoGlow (FW312)

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.

The short answer

The Omnilux Contour Face emits at 633 nm, 830 nm. The Shark CryoGlow (FW312) emits at 415 nm, 630 nm, 830 nm. Both cover red and near-infrared, the two ranges with the strongest published evidence for skin.

Only the Omnilux Contour Face publishes an irradiance figure (~30 mW/cm²). The Shark CryoGlow (FW312) does not, so the dose the two masks deliver cannot be compared.

Side by side

The specifications

Manufacturer-published specifications, checked 2026.
Specification Omnilux Contour Face Shark CryoGlow (FW312)
Wavelengths633 nm830 nm415 nm630 nm830 nm
LEDs132160+ (multi-zone)
Published irradiance~30 mW/cm²Not published
Dose per session~18 J/cm²—
Session10 min8 min
ModesSingle programme, 3–5×/week3 targeted programmes + under-eye cooling
RegulatoryFDA cleared · CE · TGA (Australia)FDA cleared · CE/UKCA
FitFlexible siliconeRigid, multi-zone
PowerRechargeable controllerCorded USB-C (cooling needs power)
Price (EU)€453.75€379.99

“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 Omnilux Contour Face emits at 633 nm, 830 nm. The Shark CryoGlow (FW312) emits at 415 nm, 630 nm, 830 nm. Both cover red and near-infrared, the two ranges with the strongest published evidence for skin.
LED count
The Shark CryoGlow (FW312) carries more diodes: 160 against 132. Diode count sets how evenly light reaches the face — a coverage figure, not an efficacy figure.
Published irradiance
Only the Omnilux Contour Face publishes an irradiance figure (~30 mW/cm²). The Shark CryoGlow (FW312) does not, so the dose the two masks deliver cannot be compared.
Regulatory
Neither prints a searchable 510(k) number; both state their clearance without one. These devices are FDA cleared, not FDA approved — clearance is a safety and manufacturing signal, not proof of results.
Session and modes
The Omnilux Contour Face runs 10 min per session (single programme, 3–5×/week). The Shark CryoGlow (FW312) runs 8 min (3 targeted programmes + under-eye cooling).
Fit and power
Omnilux Contour Face: flexible silicone; rechargeable controller. Shark CryoGlow (FW312): rigid, multi-zone; corded USB-C (cooling needs power).

Evidence notes

What the specifications don’t tell you

Omnilux Contour Face

The Omnilux Contour Face uses 132 LEDs at 633 nm, 830 nm, in sessions of 10 min.

The Omnilux LED platform is referenced across 40+ peer-reviewed papers over 20+ years — the deepest clinical heritage in the category, though consumer-mask-specific data is still brand-linked.

Shark CryoGlow (FW312)

The Shark CryoGlow (FW312) uses 160+ (multi-zone) LEDs at 415 nm, 630 nm, 830 nm, in sessions of 8 min.

Two disclosed brand-run 12-week studies — more published data than most rivals here. The under-eye cooling is a comfort feature, not a light mechanism.

Questions

Common questions

What is the main specification difference between the Omnilux Contour Face and the Shark CryoGlow (FW312)?

The Omnilux Contour Face emits at 633 nm, 830 nm. The Shark CryoGlow (FW312) emits at 415 nm, 630 nm, 830 nm. Both cover red and near-infrared, the two ranges with the strongest published evidence for skin.

Only the Omnilux Contour Face publishes an irradiance figure (~30 mW/cm²). The Shark CryoGlow (FW312) does not, so the dose the two masks deliver cannot be compared.

Which has more LEDs, the Omnilux Contour Face or the Shark CryoGlow (FW312)?

The Shark CryoGlow (FW312) carries more diodes: 160 against 132. Diode count sets how evenly light reaches the face — a coverage figure, not an efficacy figure.

Are the Omnilux Contour Face and the Shark CryoGlow (FW312) FDA cleared?

Omnilux Contour Face: FDA cleared · CE · TGA (Australia). Shark CryoGlow (FW312): FDA cleared · CE/UKCA. 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.