# K240780: InMode RF System

- Pathway: 510(k) (Traditional)
- Applicant: InMode, Ltd.
- Decided: Jul 24, 2024 after 125 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: 23 generations back to K943450 (1995). 264 ancestors in all.
3 later devices descend from it; 3 cite it directly.
0 of 268 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K233642: InMode RF System, InMode, Ltd. (2024) Summary page 4.

## Most influential descendants
- K251435: InbellaIgnite RF System (2026), 0 descendants of its own
- K251254: Ignite RF System (2026), 0 descendants of its own
- K243737: Inbella RF System (2025), 0 descendants of its own

## Indications for use
The InMode RF System is indicated for use in dermatological and general surgical procedures where coagulation/contraction of soft tissue or hemostasis is needed.

Source page: https://510kreport.com/device/K240780
Methodology: https://510kreport.com/methodology