Remade USA, LLC - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Remade USA, LLC has 1 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Last cleared in 2021. Active since 2021. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Remade USA, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
1 devices