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.

Biogend Therapeutics Co., Ltd.

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

Total Devices1
Categories1
Latest Approval2024-03-06
TypeNumberDevice NameCodeDate
510(k) K233075 “BioGend” Interbody Fusion System 001 Cage MAX 2024-03-06 View