Vjuvenate, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vjuvenate, LLC - FDA 510(k) Cleared Devices
Recent clearances: GLISSANT Intimate Lubricant
1
Total
1
Cleared
0
Denied
Vjuvenate, LLC has 1 FDA 510(k) cleared medical devices. Based in Santa Monica, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Vjuvenate, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vjuvenate, LLC
1 devices