Dermatech LaserCap™
FDA 510(k) Cleared Low-Level Laser Therapy System
The Dermatech LaserCap™ is an FDA 510(k) cleared, Class II medical device designed to promote hair growth in men and women experiencing androgenetic alopecia (pattern hair loss).
Engineered with precision low-level laser therapy (LLLT), the system delivers clinically recognized 650nm red laser light directly to the scalp to stimulate hair follicles and support natural hair regrowth.
Advanced Photobiostimulation Technology
650nm medical-grade wavelength
82 precision laser diodes
5mW output per diode (Class 3R)
Full-scalp coverage dome design
Continuous & pulse treatment modes
 
This optimized wavelength penetrates scalp tissue to stimulate cellular activity within hair follicles, supporting increased hair density and thickness over time.
Indications for Use
The Dermatech LaserCap™ is FDA-cleared to promote hair growth in:
Males with androgenetic alopecia (Norwood-Hamilton IIa–V)
Females with androgenetic alopecia (Ludwig I–II)
Fitzpatrick Skin Types I–IV
 
Treatment Protocol
30 minutes per session
3 times per week
Visible improvement typically observed after consistent use over 16 weeks
Maintenance use recommended to sustain results
Safety & Regulatory Compliance
FDA 510(k) Cleared
Class II Medical Device
Laser Class 3R compliant
Manufactured in ISO-certified facility
Electrical Safety: Class II, Type BF