Medical Device Manufacturer · US , Elkhart , IN

Heraeus Kulzer, Inc. - FDA 510(k) Cleared Devices

145 submissions · 145 cleared · Since 1988

Recent clearances: FLEXITIME FLOW, HKBOND 2006, MONDIAL

145

Total

145

Cleared

Denied

Heraeus Kulzer, Inc. has 145 FDA 510(k) cleared medical devices. Based in Elkhart, US.

Historical record: 145 cleared submissions from 1988 to 2009. Primary specialty: Dental.

Browse the FDA 510(k) cleared devices submitted by Heraeus Kulzer, Inc. Filter by specialty or product code using the sidebar.

Heraeus Kulzer, Inc. 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 - Heraeus Kulzer, Inc.

145 devices

1-12 of 145

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Heraeus Kulzer, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Heraeus Kulzer, Inc.

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