Medical Device Manufacturer · US , Santa Fe Springs , CA

Dio Department Dsi, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 2006

Total

Cleared

Denied

Dio Department Dsi, Inc. has 8 FDA 510(k) cleared medical devices. Based in Santa Fe Springs, US.

Historical record: 8 cleared submissions from 2006 to 2008. Primary specialty: Dental.

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

Dio Department Dsi, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Dio Department Dsi, Inc.

8 devices

1-8 of 8