DYNAFLEX— 510(k) K103076

Name: FDA 510(k) clearance K103076
Creator: U.S. Food and Drug Administration
Published: 2011-02-23

Substantially Equivalent

Dyna Flex

FDA 510(k) clearance K103076 for DYNAFLEX, Substantially Equivalent on 2011-02-23. Applicant: Dyna Flex. Device class: 2.

Clearance details

Applicant: Dyna Flex
Product code: Code LRK
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 2010-10-18
Decision date: 2011-02-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code LRK

product code LRK

Injury: 246
Malfunction: 1,044
Total: 1,290

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.