GR Resin System MSI— 510(k) K231775

Name: FDA 510(k) clearance K231775
Creator: U.S. Food and Drug Administration
Published: 2024-08-08

Substantially Equivalent

Pro3Dure Medical

FDA 510(k) clearance K231775 for GR Resin System MSI, Substantially Equivalent on 2024-08-08. Applicant: Pro3Dure Medical. Device class: Unclassified.

Clearance details

Applicant: Pro3Dure Medical
Product code: Code MQC
Device class: Unclassified
Advisory panel: Unknown
Date received: 2023-06-16
Decision date: 2024-08-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Iserlohn, DE

Download summary PDF View on FDA.gov ↗

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Adverse events under product code MQC

product code MQC

Injury: 377
Total: 377

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.