Remvia is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Remvia - FDA 510(k) Cleared Devices
Recent clearances: Remvia NightGuard
1
Total
1
Cleared
0
Denied
Remvia has 1 FDA 510(k) cleared medical devices. Based in St. Louis, US.
Latest FDA clearance: Dec 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Remvia Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Remvia
1 devices