Plus EV Holdings Dba Intimate Rose is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Plus EV Holdings Dba Intimate Rose - FDA 510(k) Cleared Devices
Recent clearances: Intimate Rose Vaginal Dilators, Intimate Rose Vaginal Dilators, Intimate Rose Kegel Exercise System
3
Total
3
Cleared
0
Denied
Plus EV Holdings Dba Intimate Rose has 3 FDA 510(k) cleared medical devices. Based in North Kansas City, US.
Latest FDA clearance: Aug 2024. Active since 2020. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Plus EV Holdings Dba Intimate Rose Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Third Party Review Group, LLC and Q-Metrics, LLC.
FDA 510(k) Regulatory Record - Plus EV Holdings Dba Intimate Rose
3 devices