Carl Zeiss Meditec Cataract Technology, Inc. - FDA 510(k) Cleared Dev...
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.
FDA 510(k) cleared devices by Carl Zeiss Meditec Cataract...
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