# K071872: Velashape

- Pathway: 510(k) (Traditional)
- Applicant: Syneron Medical, Ltd.
- Decided: Aug 22, 2007 after 47 days
- Product code: NUV (Massager, Vacuum, Light Induced Heating)
- 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: 13 generations back to K943450 (1995). 55 ancestors in all.
127 later devices descend from it; 7 cite it directly.
0 of 183 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050397: Velasmooth, Shaper, Syneron Medical, Ltd. (2005) Summary page 1.
- K070092: Modification to Velasmooth, Shaper, Syneron Medical, Ltd. (2007). Cleared while this submission was under review Summary page 1.

## Most influential descendants
- K080300: Cutera Multimodal Cellulite Product (Cmmcd) (2008), 101 descendants of its own
- K090221: Reaction System (2009), 54 descendants of its own
- K082622: Alma Lasers Accent B-Shape Massager Handpiece/Module (2009), 45 descendants of its own
- K133837: Viora V-Total (2014), 33 descendants of its own
- K142093: V20 System (2014), 32 descendants of its own

## Indications for use
The VelaShape is indicated for the relief of minor muscle aches and pain, relief of muscle spasm, temporary improvement of local blood circulation, temporary reduction in the appearance of cellulite, and for temporary reduction of thighs circumferences.

Source page: https://510kreport.com/device/K071872
Methodology: https://510kreport.com/methodology