Medical Device Manufacturer · US , Lakewood , NJ

Dgi Technologies - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2019

Total

Cleared

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.

FDA 510(k) cleared devices by Dgi Technologies

2 devices

1-2 of 2