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

Axiom Usa., Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K033015 AXIOM BIOLASER LLLT SERIES-3NHN2003-11-25 View
510(k) K030622 AXIOM BIOLASER LLLT SERIES-1NHN2003-09-09 View
510(k) K022602 DRX3000ITH2003-01-23 View
510(k) K023160 DRX5000ITH2002-12-20 View
↑