Inmode MD , Ltd.
Inmode MD , Ltd. has 0 FDA recalls, 0 inspections, 21 510(k) clearances and 0 compliance actions on record.
- Latest 510(k)
- Jul 12, 2021
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Summary
- Recalls
- 0
- 510(k) Clearances
- 21
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K210492 | InMode RF Pro System | Jul 12, 2021 |
| K192695 | InMode System with the Morpheus8 (Fractora) Applicators | Dec 27, 2019 |
| K191855 | EmFace Device | Oct 29, 2019 |
| K183450 | EmBody System | Jun 20, 2019 |
| K182325 | InMode RF System | Sep 26, 2018 |
| K180719 | InMode Diolaze System | Jun 14, 2018 |
| K180189 | InMode System with Fractora3D/3D-90 Applicators | Jun 1, 2018 |
| K173677 | InMode VLaze | Feb 23, 2018 |
| K172302 | InMode PLUS System | Dec 8, 2017 |
| K171593 | InMode RF System | Oct 10, 2017 |
| K170738 | InMode Diolaze XL | Aug 7, 2017 |
| K163190 | InMode RF System | Dec 12, 2016 |
| K160329 | InMode System MiniFX Handpiece | Aug 19, 2016 |
| K153568 | InMode Plus System | Jul 12, 2016 |
| K151793 | InMode RF System | Feb 19, 2016 |
| K151273 | InMode FRF Applicator | Jan 4, 2016 |
| K142952 | InMode Diolaze Device | Jan 13, 2015 |
| K140926 | INMODE WMFACE DEVICE | Dec 3, 2014 |
| K131362 | INMODE WMBODY DEVICE | Oct 8, 2013 |
| K123860 | INMODE SR IPL DEVICE | Apr 2, 2013 |