Myblend - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Myblend has 1 FDA 510(k) cleared medical devices. Based in Neuilly-Sur-Seine, FR.
Last cleared in 2023. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Myblend Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Ceiso as regulatory consultant.
FDA 510(k) Regulatory Record - Myblend
1 devices