Remi is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Remi - FDA 510(k) Cleared Devices
Recent clearances: Remi Custom Night Guard
1
Total
1
Cleared
0
Denied
Remi has 1 FDA 510(k) cleared medical devices. Based in San Francisco, US.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Remi Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Prime Path Medtech as regulatory consultant.
FDA 510(k) Regulatory Record - Remi
1 devices