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Capillus PRO

Product image: Capillus product page.
The Capillus PRO is a laser cap with 272 laser diodes. The brand's safety note gives the wavelength as 650 nm.
Capillus suggests 6 minutes every day, and the cap turns itself off when the session ends. It has a 3-year limited warranty, and new devices bought on capillus.com come with a 6-month satisfaction guarantee. The FDA record shows a 510(k) clearance for the Capillus 272 Pro (K143199).
Its daily session is one of the shortest among the caps, but it's meant to be used every day. It costs more than the 272-diode caps from Kiierr or illumiflow. Hair loss has many causes, so see a dermatologist before you buy.
Prices
| Store | Price | Price checked / source | |
|---|---|---|---|
| Capillus (brand site) | $1699 | 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) | 6 min daily |
| Power / cordless | Not listed |
| Warranty | 3 years (limited) |
| Brand money-back terms | 6 months (new devices bought on capillus.com) |
| Wavelengths | 650 nm source 650 nm from the brand's safety note. |
| FDA status | FDA-cleared 510(k) K143199 510(k) 'Capillus 272 Pro', decided 2015-01-29; also covered in K163170. 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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