Is the Blueprint 302 Laser Diode Cap FDA-cleared?Updated 3 months ago
Yes. The Blueprint 302 Laser Diode Cap has received FDA 510(k) clearance for the treatment of Androgenetic Alopecia (pattern hair loss) in both men and women. It’s cleared for:
Men with Norwood-Hamilton Classifications IIa-V
Women with Ludwig-Savin Classifications I-1 to I-4, II-1, II-2, or Frontal
Fitzpatrick Skin Types I-IV (fair to medium tones)