Venus Concept USA, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Venus Concept USA, Inc. has 11 FDA 510(k) cleared general & plastic surgery devices. Based in Sunrise, US.
Last cleared in 2022. Active since 2014.
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.
11 devices
Cleared
Dec 20, 2022
AI.ME System
General & Plastic Surgery
259d
Cleared
Apr 27, 2022
Venus BlissMAX
General & Plastic Surgery
57d
Cleared
Jan 12, 2022
Venus BlissMAX
Physical Medicine
100d
Cleared
Oct 14, 2021
Family of Venus RF Systems - Venus Freedom
General & Plastic Surgery
156d
Cleared
Jun 26, 2020
Venus Viva MD Device
General & Plastic Surgery
56d
Cleared
Jun 09, 2020
Venus Epileve
General & Plastic Surgery
75d
Cleared
Apr 01, 2020
Venus VivaTM
General & Plastic Surgery
345d
Cleared
Sep 06, 2019
Venus Legacy Pro Device
General & Plastic Surgery
88d
Cleared
Jun 25, 2019
Venus Bliss
General & Plastic Surgery
95d
Cleared
Feb 01, 2019
Family of Venus RF Systems - Heal
General & Plastic Surgery
182d
Cleared
Dec 19, 2014
Legacy BX
General & Plastic Surgery
74d