Medical Device Manufacturer · US , Newport Beach , CA

Koroad America - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2017
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.

FDA 510(k) Regulatory Record - Koroad America

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