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iRESTORE Essential
Product image: iRESTORE product page.
The iRESTORE Essential is the brand's entry-level hair helmet, with 120 diodes (51 lasers and 69 LEDs) at 655 nm.
iRESTORE suggests 25-minute sessions every other day. The helmet is hands-free, includes a 2-year warranty (a 4-year plan is sold separately) and comes with a 12-month guarantee.
It's the lowest-priced iRESTORE, with longer sessions and fewer diodes than the Professional or Elite. iRESTORE says its devices are FDA-cleared; we haven't matched a 510(k) to this exact model. Hair loss has many causes, so see a dermatologist before you buy.
Prices
| Store | Price | Price checked / source | |
|---|---|---|---|
| iRESTORE (brand site) | $799 | 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 | 120 (51 lasers + 69 LEDs) |
| Session (brand guidance) | 25 min every other day |
| Power / cordless | Not listed |
| Warranty | 2 years (4-year upgrade sold) |
| Brand money-back terms | 12 months |
| Wavelengths | 655 nm source |
| FDA status | Brand says cleared Brand says its devices are FDA 510(k)-cleared. iRESTORE 510(k)s exist (e.g. K151662 'iRestore'); we haven't matched one to the Essential model. FDA record or source |
"Brand says cleared" means the brand or a retailer says it's FDA-cleared, but we haven't matched this exact product to a 510(k) record. 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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