Carl Zeiss Meditec Cataract Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Carl Zeiss Meditec Cataract Technology, Inc. - FDA 510(k) Cleared Dev...
Recent clearances: MICOR 700 with Auto I/A, MICOR 700 System (N/A), MICOR Lens Fragmentation System
7
Total
7
Cleared
0
Denied
Carl Zeiss Meditec Cataract Technology, Inc. has 7 FDA 510(k) cleared medical devices. Based in Reno, US.
Latest FDA clearance: Aug 2025. Active since 2019. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Carl Zeiss Meditec Cataract Technology, Inc. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by GSM Services and GSM Services, Inc..
FDA 510(k) Regulatory Record - Carl Zeiss Meditec Cataract Technology, Inc.
7 devices
Cleared
Aug 08, 2025
MICOR 700 with Auto I/A
Ophthalmic
281d
Cleared
Jun 11, 2025
MICOR 700 System (N/A)
Ophthalmic
267d
Cleared
Sep 09, 2022
MICOR Lens Fragmentation System
Ophthalmic
261d
Cleared
Aug 24, 2022
miCOR System Lens Fragmentation System
Ophthalmic
29d
Cleared
Oct 15, 2020
xPORT S Lens Fragmentation System
Ophthalmic
261d
Cleared
Jul 31, 2020
xPORT 304 (miCOR) System Lens Fragmentation System
Ophthalmic
147d
Cleared
Aug 13, 2019
xPORT Lens Fragmentation System
Ophthalmic
117d