ATLANTIS ISUS Implant Suprastructures— 510(k) K160207

Substantially Equivalent

Dentsply International, Inc.

FDA 510(k) clearance K160207 for ATLANTIS ISUS Implant Suprastructures, Substantially Equivalent on 2016-09-21. Applicant: Dentsply International, Inc..

Clearance details

Applicant: Dentsply International, Inc.
Product code: Code NHA
Advisory panel: Dental
Date received: 2016-01-28
Decision date: 2016-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: York, PA, US

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Adverse events under product code NHA

product code NHA

Injury: 1,270
Malfunction: 2,860
Total: 4,130

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.