Vmi Tecnologias Ltda is one of 50 FDA 510(k) medical device manufacturers from Brazil in the dataset, ranked by real submission volume.
Vmi Tecnologias Ltda - FDA 510(k) Cleared Devices
Recent clearances: Digimamo D, Apolo D / Apolo S, AQUILA 320 D / AQUILA 320 S
3
Total
3
Cleared
0
Denied
Vmi Tecnologias Ltda has 3 FDA 510(k) cleared medical devices. Based in Aparecido De Oliveira, Lagoa Santa, BR.
Last cleared in 2022. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Vmi Tecnologias Ltda Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Kamm & Associates and Kamm and Associates.
FDA 510(k) Regulatory Record - Vmi Tecnologias Ltda
3 devices