BECE CAD ZIRKON HT+— 510(k) K132102

Name: FDA 510(k) clearance K132102
Creator: U.S. Food and Drug Administration
Published: 2013-11-12

Substantially Equivalent

Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

FDA 510(k) clearance K132102 for BECE CAD ZIRKON HT+, Substantially Equivalent on 2013-11-12. Applicant: Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO. Device class: 2.

Clearance details

Applicant: Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO
Product code: Code EIH
Device class: Class 2
Regulation: 21 CFR 872.6660
Advisory panel: Dental
Date received: 2013-07-08
Decision date: 2013-11-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bremen, 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 Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & CO

view all

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