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.

Neolight, LLC

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

Total Devices2
Categories2
Latest FDA decision2023-09-06
TypeNumberDevice NameCodeDateActions
510(k) K223575 Phoenix ICON, Phoenix ICON GOHKI2023-09-06 View
510(k) K170585 SkylifeLBI2017-10-27 View