Medical Device Manufacturer · US , Coralville , IA

Digital Diagnostics, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied

Digital Diagnostics, Inc. has 2 FDA 510(k) cleared medical devices. Based in Coralville, US.

Last cleared in 2022. Active since 2021. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by Digital Diagnostics, Inc. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.

FDA 510(k) Regulatory Record - Digital Diagnostics, Inc.
2 devices
1-2 of 2
Filters
All2 Ophthalmic 2