Medical Device Manufacturer · US , Grand Rapids , MI

Ranir/Dcp Corp. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1992

Total

Cleared

Denied

Ranir/Dcp Corp. has 6 FDA 510(k) cleared medical devices. Based in Grand Rapids, US.

Historical record: 6 cleared submissions from 1992 to 1995. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Ranir/Dcp Corp. Filter by specialty or product code using the sidebar.

Ranir/Dcp Corp. 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 - Ranir/Dcp Corp.

6 devices

1-6 of 6