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Hairmax PowerFlex 272 Laser Cap
Product image: Hairmax product page.
The Hairmax PowerFlex 272 is a flexible laser cap with 272 lasers and no LEDs.
Hairmax suggests 7 minutes, three days a week. It's cordless, running on a rechargeable battery and controller, with a silicone comfort liner. The brand's page gives the wavelength as 655 nm in one place and 650 nm in another.
It's at the higher end on price for the caps we list. Hairmax says it's FDA-cleared, but we haven't matched a 510(k) to the PowerFlex 272 by name. Hair loss has many causes, so see a dermatologist before you buy.
Prices
| Store | Price | Price checked / source | |
|---|---|---|---|
| Hairmax (brand site) | $1799 | 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 | Cap source |
|---|---|
| Light source | Laser diodes |
| Diode count | 272 |
| Session (brand guidance) | 7 min, 3× a week |
| Power / cordless | Cordless (rechargeable battery and controller) |
| Warranty | Not listed |
| Brand money-back terms | Money-back guarantee (period not stated on page) |
| Wavelengths | 655 nm source Brand page says 655 nm in its FAQ and 650 nm in a feature list. |
| FDA status | Brand says cleared Brand says FDA-cleared; we haven't matched a Hairmax 510(k) to the PowerFlex 272 by name. 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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