Cuttersil Activator Universal Plus

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K080338 ↗

FDA Product Code

ELW

FDA applicant

Heraeus Kulzer,GmbH

Device Class

Class II

Regulation

21 CFR Part 872.3660

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

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See all devices from Heraeus Kulzer, Inc. →