# K041103: Acnelift

- Pathway: 510(k) (Traditional)
- Applicant: Inner Act, LLC
- Decided: Jul 27, 2004 after 91 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K013623 (2002). 2 ancestors in all.
116 later devices descend from it; 2 cite it directly.
0 of 119 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K030883: Omnilux Blue, Photo Therapeutics Limited (2003) Summary page 1.

## Most influential descendants
- K060792: Illumimed (2006), 115 descendants of its own
- K083183: Aklarus Phototherapy System (2009), 91 descendants of its own
- K111286: Quasar Calypso (2012), 76 descendants of its own
- K162098: LED Phototherapy Device (2017), 75 descendants of its own
- K122237: Biophotas Lifelight (2013), 71 descendants of its own

## Indications for use
AcneLiftTM is generally indicated for the treatment of dermatological conditions and specifically indicated for the treatment of moderate inflammatory acne vulgaris.

Source page: https://510kreport.com/device/K041103
Methodology: https://510kreport.com/methodology