Inmode MD , Ltd. - FDA 510(k) Cleared Devices
21
Total
21
Cleared
0
Denied
Inmode MD , Ltd. has 21 FDA 510(k) cleared general & plastic surgery devices. Based in Kfar Saba, IL.
Last cleared in 2021. Active since 2013.
Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Inmode MD , Ltd.
21 devices
Cleared
Jul 12, 2021
InMode RF Pro System
General & Plastic Surgery
143d
Cleared
Dec 27, 2019
InMode System with the Morpheus8 (Fractora) Applicators
General & Plastic Surgery
92d
Cleared
Oct 29, 2019
EmFace Device
General & Plastic Surgery
111d
Cleared
Jun 20, 2019
EmBody System
General & Plastic Surgery
190d
Cleared
Sep 26, 2018
InMode RF System
General & Plastic Surgery
30d
Cleared
Jun 14, 2018
InMode Diolaze System
General & Plastic Surgery
87d
Cleared
Jun 01, 2018
InMode System with Fractora3D/3D-90 Applicators
General & Plastic Surgery
129d
Cleared
Feb 23, 2018
InMode VLaze
General & Plastic Surgery
85d
Cleared
Dec 08, 2017
InMode PLUS System
General & Plastic Surgery
130d
Cleared
Oct 10, 2017
InMode RF System
General & Plastic Surgery
132d
Cleared
Aug 07, 2017
InMode Diolaze XL
General & Plastic Surgery
150d
Cleared
Dec 12, 2016
InMode RF System
General & Plastic Surgery
28d