REVOIS IMPLANT SYSTEM— 510(k) K063106

Name: FDA 510(k) clearance K063106
Creator: U.S. Food and Drug Administration
Published: 2007-06-11

Substantially Equivalent

Curasan AG

FDA 510(k) clearance K063106 for REVOIS IMPLANT SYSTEM, Substantially Equivalent on 2007-06-11. Applicant: Curasan AG. Device class: 2.

Clearance details

Applicant: Curasan AG
Product code: Code NHA
Device class: Class 2
Regulation: 21 CFR 872.3630
Advisory panel: Dental
Date received: 2006-10-11
Decision date: 2007-06-11
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Garner,, NC, US

Download summary PDF View on FDA.gov ↗

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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.