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Inmode MD , Ltd.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
21
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K210492InMode RF Pro SystemJuly 12, 2021
K192695InMode System with the Morpheus8 (Fractora) ApplicatorsDecember 27, 2019
K191855EmFace DeviceOctober 29, 2019
K183450EmBody SystemJune 20, 2019
K182325InMode RF SystemSeptember 26, 2018
K180719InMode Diolaze SystemJune 14, 2018
K180189InMode System with Fractora3D/3D-90 ApplicatorsJune 1, 2018
K173677InMode VLazeFebruary 23, 2018
K172302InMode PLUS SystemDecember 8, 2017
K171593InMode RF SystemOctober 10, 2017
K170738InMode Diolaze XLAugust 7, 2017
K163190InMode RF SystemDecember 12, 2016
K160329InMode System MiniFX HandpieceAugust 19, 2016
K153568InMode Plus SystemJuly 12, 2016
K151793InMode RF SystemFebruary 19, 2016
K151273InMode FRF ApplicatorJanuary 4, 2016
K142952InMode Diolaze DeviceJanuary 13, 2015
K140926INMODE WMFACE DEVICEDecember 3, 2014
K131362INMODE WMBODY DEVICEOctober 8, 2013
K123860INMODE SR IPL DEVICEApril 2, 2013