# K143199: Capillus 272 Pro

- Pathway: 510(k) (Traditional)
- Applicant: Capillus, LLC
- Decided: Jan 29, 2015 after 84 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
No predicates in its family tree.
64 later devices descend from it; 8 cite it directly.
0 of 65 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) iGrow II Hair Growth System: named in the summary without a submission number
- (no number) MEP-90: named in the summary without a submission number
- (no number) Theradome LH80Pro: named in the summary without a submission number

## Most influential descendants
- K150613: LaserCap LC Pro and LC Elite (2015), 46 descendants of its own
- K153618: Capillus202 (2016), 44 descendants of its own
- K162071: IllumiFlow Laser Cap (2017), 35 descendants of its own
- K151516: Capillus82 (2015), 24 descendants of its own
- K162782: iHelmet Hair Growth System (2017), 22 descendants of its own

## Indications for use
The Capillus272 Pro is indicated to promote hair growth in females with androgenetic alopecia who have Ludwig-Savin Classifications I-II and Fitzpatrick Classification of skin phototypes of I-IV

Source page: https://510kreport.com/device/K143199
Methodology: https://510kreport.com/methodology