Reazeal Corp is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Reazeal Corp - FDA 510(k) Cleared Devices
Recent clearances: Mouth Guard (ATG0603R)
1
Total
1
Cleared
0
Denied
Reazeal Corp has 1 FDA 510(k) cleared medical devices. Based in Wilmington, US.
Last cleared in 2023. Active since 2023. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Reazeal Corp Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Sungo Management Consulting Company Limited. as regulatory consultant.
FDA 510(k) Regulatory Record - Reazeal Corp
1 devices