Globalmed Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Globalmed Technologies - FDA 510(k) Cleared Devices
Recent clearances: Omnilux CLEAR
1
Total
1
Cleared
0
Denied
Globalmed Technologies has 1 FDA 510(k) cleared medical devices. Based in Napa, US.
Last cleared in 2021. Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Globalmed Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Globalmed Technologies
1 devices