# K143554: Venus Legacy CX

- Pathway: 510(k) (Traditional)
- Applicant: Venus Concept, Ltd.
- Decided: Aug 4, 2015 after 232 days
- Product code: PBX (Massager, Vacuum, Radio Frequency Induced Heat)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 16 generations back to K943450 (1995). 65 ancestors in all.
17 later devices descend from it; 7 cite it directly.
0 of 83 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090221: Reaction System, Viora, Ltd. (2009) Summary page 4.

## Most influential descendants
- K190743: Venus Bliss (2019), 4 descendants of its own
- K191528: Venus Legacy Pro Device (2019), 3 descendants of its own
- K213308: Venus BlissMAX (2022), 2 descendants of its own
- K161199: EndyMed Contour Handpiece (2016), 2 descendants of its own
- K242996: EndyMed PRO MAX (2025), 1 descendant of its own

## Indications for use
The Venus Legacy CX device is intended for the treatment of the following medical conditions; using the LB2 and LF2 applicators for delivery of non-thermal RF combined with massage and magnetic field pulses: Relief of minor muscle aches and pain, relief of muscle spasm Temporary improvement of local blood circulation Temporary reduction in the appearance of cellulite

Source page: https://510kreport.com/device/K143554
Methodology: https://510kreport.com/methodology