VISTADENT OC - VERSION 4— 510(k) K060836

Substantially Equivalent

Dentsply Intl., Inc.

FDA 510(k) clearance K060836 for VISTADENT OC - VERSION 4, Substantially Equivalent on 2006-10-27. Applicant: Dentsply Intl., Inc..

Clearance details

Applicant: Dentsply Intl., Inc.
Product code: Code LLZ
Advisory panel: Radiology
Date received: 2006-03-28
Decision date: 2006-10-27
Decision: Substantially Equivalent
Clearance type: Special
Location: York, PA, US

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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.