ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT— 510(k) K911735

Substantially Equivalent

Artech Corp.

FDA 510(k) clearance K911735 for ARTECH ARDENT IV - TYPE CLYLINDER IMPLANT, Substantially Equivalent on 1992-03-05. Applicant: Artech Corp..

Clearance details

Applicant: Artech Corp.
Product code: Code DZE
Advisory panel: Dental
Date received: 1991-04-17
Decision date: 1992-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chantilly, VA, US

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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.