Medical Device Manufacturer · US , Orange , CA

Kerr Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2000
9
Total
9
Cleared
0
Denied

Kerr Corp. has 9 FDA 510(k) cleared medical devices. Based in Orange, US.

Historical record: 9 cleared submissions from 2000 to 2009. Primary specialty: Dental.

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

FDA 510(k) Regulatory Record - Kerr Corp.

9 devices
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