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.

Carl Zeiss Meditec Cataract Technology, Inc.

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7
Categories1
Latest FDA decision2025-08-08
TypeNumberDevice NameCodeDateActions
510(k) K243395 MICOR 700 with Auto I/AHQC2025-08-08 View
510(k) K242801 MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185)HQC2025-06-11 View
510(k) K214028 MICOR Lens Fragmentation SystemHQC2022-09-09 View
510(k) K222236 miCOR System Lens Fragmentation SystemHQC2022-08-24 View
510(k) K200207 xPORT S Lens Fragmentation SystemHQC2020-10-15 View
510(k) K200584 xPORT 304 (miCOR) System Lens Fragmentation SystemHQC2020-07-31 View
510(k) K191024 xPORT Lens Fragmentation SystemHQC2019-08-13 View
↑