# K120510: Transcend

- Pathway: 510(k) (Traditional)
- Applicant: Syneron Medical, Ltd.
- Decided: Jul 19, 2013 after 514 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- 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). 103 ancestors in all.
18 later devices descend from it; 3 cite it directly.
0 of 122 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K071872: Velashape, Syneron Medical, Ltd. (2007) Summary page 1.
- K082622: Alma Lasers Accent B-Shape Massager Handpiece/Module, Alma Lasers, Ltd. (2009) Summary page 1.

## Most influential descendants
- K163415: SlimShape System (2017), 14 descendants of its own
- K192224: BTL-899 (2019), 8 descendants of its own
- K143559: XP1000 RF (2015), 7 descendants of its own
- K202199: BTL-899ST (2021), 6 descendants of its own
- K162512: truSculpt (2016), 5 descendants of its own

## Indications for use
The Transcend is Indicated for temporary reduction in circumference of the abdomen

Source page: https://510kreport.com/device/K120510
Methodology: https://510kreport.com/methodology