# K233642: InMode RF System

- Pathway: 510(k) (Traditional)
- Applicant: InMode, Ltd.
- Decided: Mar 20, 2024 after 128 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: 22 generations back to K943450 (1995). 263 ancestors in all.
4 later devices descend from it; 1 cites 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)
- K182325: InMode RF System, Inmode MD, Ltd. (2018) Summary page 4.
- K231790: The InMode System with the Morpheus8 Applicators, InMode, Ltd. (2023) Summary page 4.

## Most influential descendants
- K240780: InMode RF System (2024), 3 descendants of its own
- 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/K233642
Methodology: https://510kreport.com/methodology