# K131362: Inmode Wmbody Device

- Pathway: 510(k) (Traditional)
- Applicant: Inmode MD, Ltd.
- Decided: Oct 8, 2013 after 148 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: 16 generations back to K943450 (1995). 65 ancestors in all.
17 later devices descend from it; 3 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 1.

## Most influential descendants
- K183450: EmBody System (2019), 8 descendants of its own
- K160329: InMode System MiniFX Handpiece (2016), 7 descendants of its own
- K201285: InMode Evolve System with the Tone Applicator (2021), 6 descendants of its own
- K210877: Evolve System with the T3 Applicator (2021), 5 descendants of its own
- K170637: sensiFirm (2017), 3 descendants of its own

## Indications for use
The InMode WIMbody device is intended for the treatment of the following medical conditions, using the WIMbady applicator fr delivering non-thermal RW combined with message: Relief of minor muscle aches and pains, relief of muscle spasma, temporary improvement of blood circulation; and Temporary reduction in the appearance of cellulite.

Source page: https://510kreport.com/device/K131362
Methodology: https://510kreport.com/methodology