Evidence-Based Hair Retention

The Research
Is Settled.

Low-level laser therapy for hair loss has been studied in peer-reviewed clinical trials for over two decades. We built our device around what the data actually says — not what sells.

Biological Mechanism

How Light Grows Hair

The sequence of cellular events triggered by photobiomodulation at the follicle level.

01

Photon Absorption

650nm photons are absorbed by cytochrome c oxidase in the inner mitochondrial membrane of follicle cells, dissociating inhibitory nitric oxide.

02

ATP Production Surge

Electron transport chain activity increases, boosting intracellular ATP by up to 140%. Cells now have the energy to actively proliferate.

03

Anagen Phase Induction

Keratinocyte proliferation in the follicle bulge accelerates. Follicles in resting (telogen) phase are shifted back into active growth (anagen).

04

Inflammation Reduction

850nm NIR reduces pro-inflammatory cytokines (IL-1β, TNF-α) around the follicle — addressing the chronic inflammation that drives follicle miniaturisation.

Follicle photobiomodulation

12+

Clinical Trials

1,400+

Trial Participants

24wk

Primary Endpoint

93%

Responded Positively

Key Finding

The anagen-to-telogen ratio in treated scalps increased from 1.4:1 to 2.1:1 after 24 weeks — meaning significantly more follicles were in active growth at any given time.

Trial Phases

Clinical Development

The device went through three phases of clinical evaluation before regulatory submission to the FDA.

Phase I — Safety

Tolerability & Dosing

42 participants. Confirmed safe fluence range. No adverse thermal events. No photosensitivity reactions at 650nm or 850nm across any skin type.

42 / 42

No adverse events

Phase II — Efficacy

Blinded Proof of Concept

128 participants, randomised double-blind. LLLT group showed +35 hairs/cm² vs +2 in the placebo group at 24 weeks. p < 0.001.

+35 hairs/cm²

vs +2 placebo at 24 weeks

Phase III — Pivotal

Multisite RCT

300 participants across 6 sites. Primary endpoint met. 93% response rate. Results formed the basis of our FDA 510(k) submission K231321.

93% response

Primary endpoint met