VITA YZ Multi Translucent— 510(k) K243940

Name: FDA 510(k) clearance K243940
Creator: U.S. Food and Drug Administration
Published: 2025-02-21

Substantially Equivalent

Vita Zahnfabrik H.Rauter GmbH & Co.

FDA 510(k) clearance K243940 for VITA YZ Multi Translucent, Substantially Equivalent on 2025-02-21. Applicant: Vita Zahnfabrik H.Rauter GmbH & Co.. Device class: 2.

Clearance details

Applicant: Vita Zahnfabrik H.Rauter GmbH & Co.
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2024-12-20
Decision date: 2025-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bad Sackingen, DE

Download summary PDF View on FDA.gov ↗

Recent devices under product code EIH

view all

K262074 — Any-Zircos2026-08-21
K262239 — Obsidian® Press Over Zirconia2026-07-30
K261046 — Dental Zirconia Blank & Coloring Liquid2026-07-17
K262195 — Dandy Ceramic Stain and Glaze2026-06-30
K260918 — Zolid Lunaris2026-06-29

More clearances from Vita Zahnfabrik H.Rauter GmbH & Co.

view all

K180703 — VITA YZ ST and VITA YZ XT2018-08-01
K153645 — VITA ENAMIC Implant Solutions (IS)2016-06-30
K152373 — VITA VM LC Flow2015-12-30
K132070 — VITA SUPRINITY(R)2014-01-31
K122269 — ENAMIC2012-12-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.