# K140926: Inmode Wmface Device

- Pathway: 510(k) (Traditional)
- Applicant: Inmode MD, Ltd.
- Decided: Dec 3, 2014 after 236 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: 15 generations back to K943450 (1995). 88 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 92 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083461: Imagine TC Skin Therapy System, Endymion Medical, Ltd. (2009) Summary page 4.

## Most influential descendants
- K221571: InMode Multi-system (2022), 2 descendants of its own
- K251632: Optimas MAX System (2025), 1 descendant of its own
- K252215: InbellaMAX System (2025), 0 descendants of its own

## Indications for use
The InMode WMface device is intended for use in dermatologic procedures, for noninvasive treatment of mild to moderate facial wrinkles and rhytides.

Source page: https://510kreport.com/device/K140926
Methodology: https://510kreport.com/methodology