ZIRKONZAHN.Implant-Planner, ZIRKONZAHN.Implant-Planner Practice, CAD/CAM STL Converter, CAD/CAM Z-Tray— 510(k) K203765

Name: FDA 510(k) clearance K203765
Creator: U.S. Food and Drug Administration
Published: 2021-07-20

Substantially Equivalent

Zirkonzahn Srl

FDA 510(k) clearance K203765 for ZIRKONZAHN.Implant-Planner, ZIRKONZAHN.Implant-Planner Practice, CAD/CAM STL Converter, CAD/CAM Z-Tray, Substantially Equivalent on 2021-07-20. Applicant: Zirkonzahn Srl. Device class: 2.

Clearance details

Applicant: Zirkonzahn Srl
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2020-12-23
Decision date: 2021-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Gais, IT

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

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