# K172302: InMode PLUS System

- Pathway: 510(k) (Traditional)
- Applicant: Inmode MD, Ltd.
- Decided: Dec 8, 2017 after 130 days
- Product code: PBX (Massager, Vacuum, Radio Frequency Induced Heat)
- 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: 21 generations back to K943450 (1995). 313 ancestors in all.
13 later devices descend from it; 3 cite it directly.
0 of 327 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K153568: InMode Plus System, Inmode MD, Ltd. (2016) Summary page 5.

## Most influential descendants
- K183450: EmBody System (2019), 8 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
- K221571: InMode Multi-system (2022), 2 descendants of its own
- K251632: Optimas MAX System (2025), 1 descendant of its own

## Indications for use
The InMode PLUS System with the PLUS/PLUS90/PLUS-PLUS Hand pieces is indicated for the temporary relief of minor muscle aches and pain. temporary relief of muscle spasm. and temporary improvement of local blood circulation

Source page: https://510kreport.com/device/K172302
Methodology: https://510kreport.com/methodology