Nti Clenching Suppression System

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K981546 ↗

FDA Product Code

MQC

Device Class

U

Advisory Committee

Unknown

FDA Decision

SESE Substantially Equivalent

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  Class II

  FDA 510(k) K884756 Active Cleared 13 Jan 1989

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See all devices from Heraeus Kulzer, Inc. →