Venus Concept USA, Inc.
Venus Concept USA, Inc. holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2022.
Top product codes for Venus Concept USA, Inc.
Recent clearances by Venus Concept USA, Inc.
- K221011 — AI.ME System
- K220592 — Venus BlissMAX
- K213308 — Venus BlissMAX
- K211461 — Family of Venus RF Systems - Venus Freedom
- K201164 — Venus Viva MD Device
- K200786 — Venus Epileve
- K191065 — Venus VivaTM
- K191528 — Venus Legacy Pro Device
- K190743 — Venus Bliss
- K182094 — Family of Venus RF Systems - Heal
- K142910 — Legacy BX
Data sourced from openFDA. This site is unofficial and independent of the FDA.