Inmode MD , Ltd.
Inmode MD , Ltd. holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2021.
Top product codes for Inmode MD , Ltd.
Recent clearances by Inmode MD , Ltd.
- K210492 — InMode RF Pro System
- K192695 — InMode System with the Morpheus8 (Fractora) Applicators
- K191855 — EmFace Device
- K183450 — EmBody System
- K182325 — InMode RF System
- K180719 — InMode Diolaze System
- K180189 — InMode System with Fractora3D/3D-90 Applicators
- K173677 — InMode VLaze
- K172302 — InMode PLUS System
- K171593 — InMode RF System
- K170738 — InMode Diolaze XL
- K163190 — InMode RF System
- K160329 — InMode System MiniFX Handpiece
- K153568 — InMode Plus System
- K151793 — InMode RF System
- K151273 — InMode FRF Applicator
- K142952 — InMode Diolaze Device
- K140926 — INMODE WMFACE DEVICE
- K131362 — INMODE WMBODY DEVICE
- K123860 — INMODE SR IPL DEVICE
- K123682 — INMODE HAIR REMOVAL (HR) DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.