Carl Zeiss Meditec Cataract Technologies is one of 25915 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carl Zeiss Meditec Cataract Technologies - FDA 510(k) Cleared Devices
Recent clearances: MICOR 700 System (N/A)
1
Total
1
Cleared
0
Denied
Carl Zeiss Meditec Cataract Technologies has 1 FDA 510(k) cleared medical devices. Based in Reno, US.
Latest FDA clearance: Oct 2026. Active since 2026. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Carl Zeiss Meditec Cataract Technologies Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by GSM Services, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Carl Zeiss Meditec Cataract Technologies
1 devices