Medical Device Manufacturer · US , Mchenry , IL

Kerr Corporation (Danbury) - FDA 510(k) Cleared Devices

32 submissions · 32 cleared · Since 1978

Total

Cleared

Denied

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

Historical record: 32 cleared submissions from 1978 to 2005.

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

Kerr Corporation (Danbury) 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 - Kerr Corporation (Danbury)

32 devices

1-12 of 32

M4 CONTRA-ANGLE HANDPIECE

KERR OPTIBOND, MODIFICATION

AUTOMIX DENTAL AMALGAMATOR

Ear, Nose, Throat · 147d

Kerr Corporation (Danbury) - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Kerr Corporation (Danbury)

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