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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K180719

InMode Diolaze System · Inmode MD , Ltd. · decided 2018-06-14 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
InMode AG606991AINMODE M.D LTDGEX07290016633375
Diolaze XL 810 ApplicatorAG605985AINMODE M.D LTDGEX07290016633269
Diolaze XL 810/1064 ApplicatorAG605976AINMODE M.D LTDGEX07290016633283
Diolaze XL 755/810 ApplicatorAG605975AINMODE M.D LTDGEX07290016633276
InMode AG606992AINMODE M.D LTDGEX07290016633382