Yxoss CBR®— 510(k) K192747

Substantially Equivalent

Reoss GmbH

FDA 510(k) clearance K192747 for Yxoss CBR®, Substantially Equivalent on 2020-06-17. Applicant: Reoss GmbH.

Clearance details

Applicant: Reoss GmbH
Product code: Code JEY
Advisory panel: Dental
Date received: 2019-09-30
Decision date: 2020-06-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Filderstadt, DE

Download summary PDF View on FDA.gov ↗

Adverse events under product code JEY

product code JEY

Injury: 1,542
Malfunction: 2,292
Total: 3,834

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.