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

Clearance record K200947

InMode System with the Morhpeus8 Applicators · InMode , Ltd. · decided 2020-07-02 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Morpheus8 TIPAG607563AINMODE M.D LTDGEI07290016633443
Morpheus8 Body (Blue)AG609126AINMODE M.D LTDGEI07290016633672
Morpheus8 ApplicatorAG607401AINMODE M.D LTDGEI07290016633412