Medical Device Manufacturer · US , Newport Beach , CA

Kerr Corporation - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 2006

Recent clearances: ZenSeal Pro, Rainbow 360, SimpliShade Bulk Fill, SimpliShade Bulk Fill Flow

32
Total
32
Cleared
0
Denied

Kerr Corporation has 32 FDA 510(k) cleared dental devices. Based in Newport Beach, US.

Latest FDA clearance: Jan 2026. Active since 2006.

Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Sybron Dental Specialties as regulatory consultant.

FDA 510(k) Regulatory Record - Kerr Corporation

32 devices
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