Medical Device Manufacturer · US , Reno , NV

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

7 submissions · 7 cleared · Since 2019

Recent clearances: MICOR 700 with Auto I/A, MICOR 700 System (N/A), MICOR Lens Fragmentation System

7
Total
7
Cleared
0
Denied

FDA 510(k) Regulatory Record - Carl Zeiss Meditec Cataract Technology, Inc. Ophthalmic ✕

7 devices
1-7 of 7
Cleared Aug 08, 2025
MICOR 700 with Auto I/A
K243395 · HQC
Ophthalmic · 281d
Cleared Jun 11, 2025
MICOR 700 System (N/A)
K242801 · HQC
Ophthalmic · 267d
Cleared Sep 09, 2022
MICOR Lens Fragmentation System
K214028 · HQC
Ophthalmic · 261d
Cleared Aug 24, 2022
miCOR System Lens Fragmentation System
K222236 · HQC
Ophthalmic · 29d
Cleared Oct 15, 2020
xPORT S Lens Fragmentation System
K200207 · HQC
Ophthalmic · 261d
Cleared Jul 31, 2020
xPORT 304 (miCOR) System Lens Fragmentation System
K200584 · HQC
Ophthalmic · 147d
Cleared Aug 13, 2019
xPORT Lens Fragmentation System
K191024 · HQC
Ophthalmic · 117d
Filters
Filter by Specialty
All7 Ophthalmic 7