# K070494: Epi-C Plus

- Pathway: 510(k) (Traditional)
- Applicant: Espansione Marketing S.P.A
- Decided: May 1, 2007 after 70 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
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 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 no predicate by number.

## Most influential descendants
- K092734: E-Light Line (2010), 2 descendants of its own
- K124064: Young Again (2013), 1 descendant of its own
- K162556: Lightfusion Led System (2017), 0 descendants of its own

## Indications for use
This product is intended for dermatological use by physicians and healthcare professionals for the following: * Removal of unwanted hair in all skin types (from 570- to 1200nm filter) * Treatment of vascular and benign pigmented lesions, cutaneous lesions including warts, scars, striae and facial and leg veins (from 550 to 1200nm filter). * Treatment of Acne (from 390 to 1200nm filter)

Source page: https://510kreport.com/device/K070494
Methodology: https://510kreport.com/methodology