Zeno Ai Eco Disc

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K082257 ↗

FDA Product Code

EIH

Device Class

Class II

Regulation

21 CFR Part 872.6660

Advisory Committee

Dental

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K020192 Active Cleared 15 Mar 2002

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  FDA 510(k) K112710 Active Cleared 17 Oct 2011

See all devices from Wieland Dental + Technik GmbH & Co. KG →