Omnilux Contour Face LED Mask Review

What We Liked

• Fully wireless during sessions — no cord tethering
• Flexible silicone, shaped to sit against the face
• Manufacturer cites published photobiomodulation research behind the wavelength pair

What We Didn’t Like

• No blue light (415nm) — only red and near-infrared
• No 1072nm deep-NIR wavelength; CurrentBody Series 2 is the only catalog device with one

Who It Suits

• Anyone wanting a wireless mask
• Anyone who prefers flexible silicone over a rigid shell
• Anyone wanting red and near-infrared light without blue

Who Should Choose Something Else

• Want deep-tissue 1072nm penetration → CurrentBody Series 2
• Need blue light (415nm) → Dr. Dennis Gross DRx
• On a budget but want three wavelengths → iRestore Illumina

FDA Registry Check

This device has a clearance, and finding it takes three steps. The GUDID record for Omnilux Contour FACE — device identifier 05060534510128, filed by I-Smart Developments Limited — cites 510(k) number K191629. That clearance, issued 2019-09-12, is recorded under a different device name: faceLITE, filed by Ismart Marketing Svcs, Ltd.

Searching the 510(k) database for “Omnilux Contour” returns nothing. The brand’s other clearances cover different devices entirely. Only the GUDID record connects the mask on the shelf to the clearance that covers it.

This is not unusual. Devices are frequently cleared under the manufacturer’s name for a product later sold under a retail brand — the same pattern appears across this catalog. It does mean a buyer searching the registry under the name printed on the box will not find anything. Checked 2026-08-15; see our full clearance check for the eight searches run and what each returned.