Koroad America is one of 18984 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
1
Total
1
Cleared
0
Denied
Koroad America has 1 FDA 510(k) cleared medical devices. Based in Newport Beach, US.
Historical record: 1 cleared submissions from 2017 to 2017. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Koroad America Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Provision Consulting Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Koroad America
1 devices