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.

Raypia Co., Ltd.

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

Total Devices1
Categories1
Latest Approval2024-12-04
TypeNumberDevice NameCodeDate
510(k) K242185 Rextar Pro EHD 2024-12-04 View