# K173677: InMode VLaze

- Pathway: 510(k) (Traditional)
- Applicant: Inmode MD, Ltd.
- Decided: Feb 23, 2018 after 85 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- 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). 303 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 307 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133319: ET Lightsheer 1060, High Speed Lightsheer 1060, Lumenis, Ltd. (2014) Summary page 4.
- K160368: EVO platform, Quanta System Spa (2016) Summary page 4.
- K170738: InMode Diolaze XL, Inmode MD, Ltd. (2017) 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 VLaze is intended for the treatment of vascular lesions, including angiomas, hemangiomas, telangiectasia, port wine stains, leg veins and other benign vascular lesions.

Source page: https://510kreport.com/device/K173677
Methodology: https://510kreport.com/methodology