ANCHOR PLUS/NEO ANCHOR PLUS— 510(k) K053629

Substantially Equivalent

Kj Meditech

FDA 510(k) clearance K053629 for ANCHOR PLUS/NEO ANCHOR PLUS, Substantially Equivalent on 2006-05-31. Applicant: Kj Meditech.

Clearance details

Applicant: Kj Meditech
Product code: Code DZE
Advisory panel: Dental
Date received: 2005-12-29
Decision date: 2006-05-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Flintville, TN, 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.