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.
FDA 510(k) cleared devices by Venus Concept USA, Inc.
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