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iRESTORE Elite
Product image: iRESTORE product page.
The iRESTORE Elite is the brand's top helmet, with 500 diodes (300 lasers and 200 LEDs) across three red wavelengths: 625, 655 and 680 nm.
Sessions are shorter than the other iRESTOREs, at 12 minutes a day. It includes a 3-year warranty (a 5-year plan is sold separately) and a 12-month guarantee. The FDA record shows a 510(k) clearance (K222081).
It has the highest diode count in our hair list and is at the higher end on price at $2,699. A higher diode count doesn't by itself mean better results. Hair loss has many causes, so see a dermatologist before you buy.
Prices
| Store | Price | Price checked / source | |
|---|---|---|---|
| iRESTORE (brand site) | $2699 | Nov 1, 2026 brand store data |
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Store links go straight to the store's product page, with no affiliate tracking. Confirm the price there before you buy. See our disclosure.
Price history
We don't have a sourced price history for this device yet. The prices above are what we saw on the dates shown. A current sale price isn't necessarily the lowest this device has sold for.
Specs & regulatory status
| Type | Helmet source |
|---|---|
| Light source | Lasers + LEDs |
| Diode count | 500 (300 lasers + 200 LEDs) |
| Session (brand guidance) | 12 min daily |
| Power / cordless | Not listed |
| Warranty | 3 years (5-year upgrade sold) |
| Brand money-back terms | 12 months |
| Wavelengths | 625 nm, 655 nm, 680 nm source |
| FDA status | FDA-cleared 510(k) K222081 510(k) 'ID-510 iRestore Elite', Freedom Laser Therapy, decided 2022-10-13. FDA record or source |
"FDA-cleared" means we matched this product to a 510(k) record: the FDA cleared it as substantially equivalent to an existing device for its labelled use. FDA clearance is not FDA approval, and a listed specification isn't proof that a device works. How we check FDA status.
Terms on this page
- nm
- Nanometres, the unit for a light's wavelength (its colour). Red light is roughly 620–700 nm; near-infrared is above 700 nm.
- 510(k)
- The FDA premarket notification route. A cleared 510(k) means the FDA found the device substantially equivalent to one already on the market. It is not FDA approval.
- Diodes
- The individual light sources in a device: LEDs, which spread light, or laser diodes, which produce a narrower beam.
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