# K160285: Capillus272 Pro, Capillus272 OfficePro, Capillus82, Capillus202

- Pathway: 510(k) (Traditional)
- Applicant: Capillus, LLC
- Decided: Apr 25, 2016 after 82 days
- Product code: OAP (Laser, Comb, Hair)
- Device class: 2
- Regulation: 21 CFR 890.5500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K060305 (2007). 7 ancestors in all.
59 later devices descend from it; 8 cite it directly.
0 of 67 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122248: Igrow II Hair Growth System, Apira Science, Inc. (2012) Summary page 6.
- K140931: Igrow II Hair Growth System, Apira Science, Inc. (2014) Summary page 6.
- K142573: HairMax LaserComb, HairMax LaserComb, Lexington International, LLC (2014) Summary page 6.

## Most influential descendants
- K162071: IllumiFlow Laser Cap (2017), 35 descendants of its own
- K162782: iHelmet Hair Growth System (2017), 22 descendants of its own
- K161875: LaserCap300, LaserCap224, LaserCap120, LaserCap80 (2016), 20 descendants of its own
- K173729: Revian Red (2018), 19 descendants of its own
- K173678: Diode Laser Cap (2018), 16 descendants of its own

## Indications for use
The Capillus272 Pro, Capillus272 OfficePro, Capillus82, and Capillus202 are intended for the promotion of hair growth in females with androgenic alopecia who have Ludwig-Savin Classifications I- II, and in males with androgenic alopecia who have Norwood Hamilton Classifications IIa-V ; and both genders having Fitzpatrick Classification of Skin Phototypes I to IV.

Source page: https://510kreport.com/device/K160285
Methodology: https://510kreport.com/methodology