# K171593: InMode RF System

- Pathway: 510(k) (Traditional)
- Applicant: Inmode MD, Ltd.
- Decided: Oct 10, 2017 after 132 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
No predicates in its family tree.
15 later devices descend from it; 1 cites it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The summary cites one number, which could not be confirmed as its predicate (listed below).

## Cited in the summary but kept off the family tree
- K160193: InMode RF System. Not in FDA’s 510(k), De Novo or PMA lists as we hold them (a misreading, a typo, or a number FDA does not list), so it is kept off the family tree Summary page 4.

## Most influential descendants
- K182325: InMode RF System (2018), 14 descendants of its own
- K201150: InMode RF Multi-System (2020), 8 descendants of its own
- K210492: InMode RF Pro System (2021), 7 descendants of its own
- K233642: InMode RF System (2024), 4 descendants of its own
- K240780: InMode RF System (2024), 3 descendants of its own

## Indications for use
The InMode RF System is indicated for use in dermatological and general surgical procedures for electro-coagulation and hemostasis.

Source page: https://510kreport.com/device/K171593
Methodology: https://510kreport.com/methodology