IVOBASE HYBRID, IVOBASE HIGH IMPACT— 510(k) K103391

Substantially Equivalent

Ivoclar Vivadent, Inc.

FDA 510(k) clearance K103391 for IVOBASE HYBRID, IVOBASE HIGH IMPACT, Substantially Equivalent on 2011-02-17. Applicant: Ivoclar Vivadent, Inc..

Clearance details

Applicant: Ivoclar Vivadent, Inc.
Product code: Code EBI
Advisory panel: Dental
Date received: 2010-11-19
Decision date: 2011-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Amherst, NY, US

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Adverse events under product code EBI

product code EBI

Other: 1
Total: 1

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.