Dgi Technologies - FDA 510(k) Cleared Devices
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.
510(k) submissions have been managed by Contract In-House Consultants, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Dgi Technologies
2 devices