Dgi Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dgi Technologies - FDA 510(k) Cleared Devices
Recent clearances: Claritag Advanced, Claritag
2
Total
2
Cleared
0
Denied
Dgi Technologies has 2 FDA 510(k) cleared medical devices. Based in Lakewood, US.
Last cleared in 2023. Active since 2019. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Dgi Technologies Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Health Policy Associates and Contract In-House Consultants, LLC.
FDA 510(k) Regulatory Record - Dgi Technologies
2 devices