Zirconia Block— 510(k) K233125

Name: FDA 510(k) clearance K233125
Creator: U.S. Food and Drug Administration
Published: 2024-01-12

Substantially Equivalent

Hangzhou Ivista Medical Devices Co., Ltd.

FDA 510(k) clearance K233125 for Zirconia Block, Substantially Equivalent on 2024-01-12. Applicant: Hangzhou Ivista Medical Devices Co., Ltd.. Device class: 2.

Clearance details

Applicant: Hangzhou Ivista Medical Devices Co., Ltd.
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2023-09-27
Decision date: 2024-01-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hangzhou, CN

Download summary PDF View on FDA.gov ↗

Recent devices under product code EIH

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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

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