STRAUMANN ORTHOSYSTEM— 510(k) K060062

Name: FDA 510(k) clearance K060062
Creator: U.S. Food and Drug Administration
Published: 2006-02-03

Substantially Equivalent

Institut Straumann AG

FDA 510(k) clearance K060062 for STRAUMANN ORTHOSYSTEM, Substantially Equivalent on 2006-02-03. Applicant: Institut Straumann AG. Device class: 2.

Clearance details

Applicant: Institut Straumann AG
Product code: Code OAT
Device class: Class 2
Regulation: 21 CFR 872.3640
Advisory panel: Dental
Date received: 2006-01-09
Decision date: 2006-02-03
Decision: Substantially Equivalent
Clearance type: Special
Location: Andover, MA, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code OAT

product code OAT

Injury: 355
Total: 355

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.