Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Reoss GmbH

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest Approval2020-06-17
TypeNumberDevice NameCodeDate
510(k) K192747 Yxoss CBR® JEY 2020-06-17 View