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.

Optonol, Ltd.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K030350 EXPRESS MINI GLAUCOMA SHUNTKYF2003-03-13 View
510(k) K012852 EX-PRESS MINATURE GLAUCOMA IMPLANT, MODELS R-20, R-30, R-50, STS VERSIONSKYF2002-03-26 View
↑