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Hairmax Ultima 12 LaserComb
Product image: Hairmax product page.
The Hairmax Ultima 12 LaserComb is a handheld comb with 12 lasers at 655 nm. You slowly move it across your scalp.
Hairmax suggests about 8 minutes, three days a week. Because it's handheld, you guide the light where you want it rather than wearing a cap.
It's the lowest-priced device in our hair list. It needs more hands-on time than a cap, and with 12 lasers it covers a small area at once. Hairmax LaserComb 510(k)s exist, but we haven't confirmed which covers this model. Hair loss has many causes, so see a dermatologist before you buy.
Prices
| Store | Price | Price checked / source | |
|---|---|---|---|
| Hairmax (brand site) | $399 | 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 | Comb source |
|---|---|
| Light source | Laser diodes |
| Diode count | 12 |
| Session (brand guidance) | 8 min, 3× a week |
| Power / cordless | Not listed |
| Warranty | Not listed |
| Brand money-back terms | Money-back guarantee (period not stated on page) |
| Wavelengths | 655 nm source |
| FDA status | Brand says cleared Brand says FDA-cleared. Hairmax LaserComb 510(k)s exist (e.g. K142573); we haven't confirmed which covers the Ultima 12. 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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