Inmode , Ltd. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Inmode , Ltd. has 15 FDA 510(k) cleared general & plastic surgery devices. Based in Yokneam, IL.
Latest FDA clearance: Jan 2026. Active since 2019.
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 , Ltd.
15 devices
Cleared
Jan 15, 2026
Ignite RF System
General & Plastic Surgery
267d
Cleared
Jun 26, 2025
Optimas MAX System
General & Plastic Surgery
29d
Cleared
Nov 14, 2024
DEFINE System (AG612444A)
General & Plastic Surgery
76d
Cleared
Jul 24, 2024
InMode RF System
General & Plastic Surgery
125d
Cleared
Jun 13, 2024
InMode System with the Morpheus8 90 Applicator
General & Plastic Surgery
163d
Cleared
Mar 20, 2024
InMode RF System
General & Plastic Surgery
128d
Cleared
Oct 13, 2023
The Evolve System with the Transform Applicator
General & Plastic Surgery
143d
Cleared
Jul 20, 2023
The InMode System with the Morpheus8 Applicators
General & Plastic Surgery
30d
Cleared
Jun 30, 2022
InMode Multi-system
General & Plastic Surgery
30d
Cleared
Jul 19, 2021
Evolve System with the T3 Applicator
General & Plastic Surgery
117d
Cleared
Mar 05, 2021
InMode Evolve System with the Tone Applicator
Physical Medicine
296d
Cleared
Jul 22, 2020
InMode RF Multi-System
General & Plastic Surgery
84d