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.

M.B. Industries, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K964553 MBI CO-AXIAL ILLUMINATED RETINAL PICKMPA1997-05-13 View
510(k) K964405 MBI ILLUMINATED RETINAL PICKMPA1997-05-13 View
510(k) K961036 MBI FIBEROPTIC ENDO-ILLUMINATORMPA1996-07-15 View
↑