Reddrop DX - FDA 510(k) Cleared Devices
1
Total
0
Cleared
0
Denied
Reddrop DX has 0 FDA 510(k) cleared medical devices. Based in Fort Collins, US.
Latest FDA clearance: Mar 2024. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Reddrop DX Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Reddrop DX
1 devices