Quick Answer: Vielight’s current lineup runs from the $349 MIP 633-810 nasal device to the $5,000 Neuro Pro 2, with the brain-targeted Neuro Gamma 4 and Neuro Alpha 4 at $1,799 each and the combined Neuro Duo 4 at $2,399, per Vielight’s own store. Vielight’s Neuro Gamma line bets on 40Hz brain-wave gamma entrainment for cognition — the same underlying science behind Cognito Therapeutics’ Spectris AD, which holds FDA Breakthrough Device Designation and completed a 670-patient sham-controlled pivotal trial in 2026 before seeking clearance. Vielight’s devices, by contrast, are sold today as general wellness products under a trial the company announced back in 2019 that hasn’t yet led to a disease-specific FDA clearance.

Vielight already shows up on this site as our top pick in several nasal and condition guides — the X-Plus 4 leads our best nasal red light therapy guide and gets recommended for sinus, allergies, and off-label tinnitus use — but the brand has never had its own dedicated review covering its full lineup, including the brain-targeted Neuro devices those guides don’t mention. This one prices the whole catalog direct from Vielight’s store and looks closely at the regulatory story behind its highest-priced, most science-forward product line.

Vielight’s lineup by the numbers

The full lineup at a glance

DeviceBest forFrequency / WavelengthPrice
Vielight X-Plus 4Nasal/systemic, already our top nasal pick633nm + 810nm NIR$449
Vielight Neuro Gamma 4Focus-oriented brain stimulation40Hz / 810nm$1,799
Vielight Neuro Alpha 4Relaxation-oriented brain stimulation10Hz / 810nm$1,799
Vielight Neuro Duo 4Both frequencies in one device10Hz + 40Hz / 810nm$2,399
Vielight VagusVagus-nerve targeted stimulation810nm$699
Vielight Neuro Pro 2Fully customizable frequencyAdjustable / 810nm$5,000

Vielight Neuro Gamma 4

Focus-oriented brain stimulation · $1,799
  • Pulses 810nm near-infrared light at 40Hz through transcranial and intranasal applicators, per Vielight's own specs.
  • Marketed for focus, cognitive processing, and neural connectivity — the same 40Hz gamma-entrainment mechanism studied for Alzheimer's support, though Vielight's device itself carries no disease-specific FDA clearance.
  • Default 20-minute session, worn like a cap with an intranasal applicator clipped in alongside it.
  • Same hardware platform as Neuro Alpha 4, just a different preset frequency.
Check Vielight Neuro devices on Amazon →

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Vielight Neuro Duo 4

Both frequencies in one device · $2,399
  • Includes both the 10Hz Alpha and 40Hz Gamma drivers, so sessions can target either relaxation or focus depending on the day.
  • $1,199 cheaper than buying a separate Neuro Alpha 4 ($1,799) and Neuro Gamma 4 ($1,799), per Vielight's own pricing.
  • Same 810nm wavelength and transcranial-plus-intranasal applicator design as the single-frequency Neuro devices.
  • Vielight also sells a Neuro Duo 4 + Vagus bundle at $3,098 for buyers who want both the brain and vagus-nerve devices together.
Check the Vielight Neuro Duo on Amazon →

The 40Hz gamma question: two companies, two different paths to market

Vielight’s Neuro Gamma line is built around a specific, well-known piece of science: 40Hz gamma brain-wave entrainment, a mechanism that gained attention after MIT research suggested it could help clear amyloid plaque and support cognition in Alzheimer’s disease models. Vielight’s Neuro Gamma 4 and Neuro Duo 4 both deliver this 40Hz pulse via transcranial and intranasal near-infrared light, and the brand has been pursuing Alzheimer’s-specific research since at least 2019, when it announced a 228-subject pivotal clinical trial.

A separate company, Cognito Therapeutics, is chasing the same 40Hz gamma mechanism through a different route — synchronized light-and-sound stimulation rather than near-infrared light alone — and took a markedly different path to market. Cognito’s Spectris AD holds FDA Breakthrough Device Designation, and the company announced in 2026 that it had completed enrollment of 670 participants in the HOPE Study, a randomized, double-blind, sham-controlled pivotal trial spanning 70 U.S. sites, with topline results reported showing a measurable slowing of decline versus sham treatment. As of 2026, Cognito has not yet brought a cleared product to retail — it’s still working through the regulatory pathway.

Vielight’s Neuro devices, meanwhile, are available to buy today, classified by the FDA under the same “general wellness” category that covers ordinary red light panels — a low-risk designation that does not require proving effectiveness for any specific disease. That’s not a claim that Vielight’s devices don’t work; photobiomodulation research on gamma entrainment is real and ongoing. But it is a meaningfully different regulatory story than a device going through a sham-controlled pivotal trial before it reaches consumers. If the reason you’re considering a $1,799-$2,399 Neuro device is specifically for Alzheimer’s or dementia support, know that Vielight’s own devices have not completed the kind of trial Cognito is running, and are not FDA-cleared for that use.

Who should buy which Vielight device

Vielight’s hardware claims — wavelengths, frequencies, and pricing — check out against its own live store, and the brand genuinely pioneered both intranasal photobiomodulation and consumer gamma-entrainment devices. But the highest-priced devices in its catalog are marketed around a disease connection the company’s own regulatory status doesn’t yet support, while a competitor working the same science is still mid-trial. Buy the Neuro line as a general wellness device, not as a dementia treatment.

Red light and near-infrared devices are general wellness products, not a treatment for any specific medical condition. “FDA general wellness” is a low-risk regulatory category, not a clearance confirming individual results, and nothing here is medical advice — talk to a qualified clinician before starting any light therapy regimen, especially for cognitive or neurological concerns. Prices and specs were verified against Vielight’s own live store and Cognito Therapeutics’ public trial announcements in September/October 2026 and change without notice.