ANKYLOS— 510(k) K012681

Substantially Equivalent

Dentsply Ceramco

FDA 510(k) clearance K012681 for ANKYLOS, Substantially Equivalent on 2003-08-22. Applicant: Dentsply Ceramco.

Clearance details

Applicant: Dentsply Ceramco
Product code: Code DZE
Advisory panel: Dental
Date received: 2001-08-14
Decision date: 2003-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Burlington, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code DZE

product code DZE

Death: 28
Injury: 3,367,041
Malfunction: 19,958
Other: 13
Total: 3,387,040

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.