ODYSSEY 2.4G, DENLASER ELITE, MODEL 002-00050— 510(k) K050453

Substantially Equivalent

Ivoclar Vivadent, Inc.

FDA 510(k) clearance K050453 for ODYSSEY 2.4G, DENLASER ELITE, MODEL 002-00050, Substantially Equivalent on 2005-05-27. Applicant: Ivoclar Vivadent, Inc..

Clearance details

Applicant: Ivoclar Vivadent, Inc.
Product code: Code GEX
Advisory panel: General, Plastic Surgery
Date received: 2005-02-22
Decision date: 2005-05-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Amherst, NY, US

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Adverse events under product code GEX

product code GEX

Death: 33
Injury: 3,045
Malfunction: 12,903
Other: 25
Total: 16,006

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.