Carl Zeiss Meditec Cataract Technology, Inc.
FDA 510(k) & PMA Approved Devices — 7 products
Total Devices7
Categories1
Latest Approval2025-08-08
| Type | Number | Device Name | Code | Date | |
|---|---|---|---|---|---|
| 510(k) | K243395 | MICOR 700 with Auto I/A | HQC | 2025-08-08 | View |
| 510(k) | K242801 | MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185) | HQC | 2025-06-11 | View |
| 510(k) | K214028 | MICOR Lens Fragmentation System | HQC | 2022-09-09 | View |
| 510(k) | K222236 | miCOR System Lens Fragmentation System | HQC | 2022-08-24 | View |
| 510(k) | K200207 | xPORT S Lens Fragmentation System | HQC | 2020-10-15 | View |
| 510(k) | K200584 | xPORT 304 (miCOR) System Lens Fragmentation System | HQC | 2020-07-31 | View |
| 510(k) | K191024 | xPORT Lens Fragmentation System | HQC | 2019-08-13 | View |
No matching devices.