# Carl Zeiss Meditec Cataract Technology, Inc.

- Location (FDA's records): Reno, NV
- FDA decisions: 7 (2019–2025): 7 510(k) clearances
- Product codes: HQC (7)
- 510(k) review time since 2016: median 261 days, against 245 for FDA's reviews in the same codes and years (3 of 7 faster)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K243395: MICOR 700 with Auto I/A (Aug 8, 2025)
- K242801: MICOR 700 System (N/A); MICOR 700 drive (FG-50631); MICOR 700 extractor (FG-50621); MICOR 700 vitrector (FG-51185) (Jun 11, 2025)
- K214028: MICOR Lens Fragmentation System (Sep 9, 2022)
- K222236: miCOR System Lens Fragmentation System (Aug 24, 2022)
- K200207: xPORT S Lens Fragmentation System (Oct 15, 2020)
- K200584: xPORT 304 (miCOR) System Lens Fragmentation System (Jul 31, 2020)
- K191024: xPORT Lens Fragmentation System (Aug 13, 2019)

Source page: https://510kreport.com/company/carl-zeiss-meditec-cataract-technology