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.

Visioncare Devices, Inc.

FDA 510(k) & PMA Approved Devices — 5 products

Total Devices5
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K120170 PROCARE PLUS VITRECTOMY SYSTEMHQE2012-05-30 View
510(k) K023939 VELOCITY ADVANTAGEHQE2003-04-17 View
510(k) K971064 BAYERS BIMANUAL I/A HANDPIECESHQC1997-06-09 View
510(k) K940746 VIT CUTTER MODEL 94HQE1994-06-06 View
510(k) K904909 I/A VITROPHAGE MODEL YPR 2001HQE1991-01-28 View
↑