Medical Device Manufacturer · US , Dublin , CA

Carl Zeiss Meditec, AG - FDA 510(k) Cleared Devices

45 submissions · 44 cleared · Since 2004
45
Total
44
Cleared
0
Denied

FDA 510(k) cleared devices by Carl Zeiss Meditec, AG Ophthalmic ✕

32 devices
1-12 of 32
Cleared Sep 06, 2024
VISULAS combi
K233911 · HQF
Ophthalmic · 269d
Cleared Mar 08, 2024
RESCAN 700
K233421 · OBO
Ophthalmic · 150d
Cleared Dec 21, 2023
CALLISTO eye
K232944 · NFJ
Ophthalmic · 92d
Cleared Aug 28, 2023
CALLISTO eye
K231676 · NFJ
Ophthalmic · 80d
Cleared Jul 31, 2023
QUATERA 700
K230858 · HQC
Ophthalmic · 124d
Cleared Aug 15, 2022
FORUM
K213527 · NFJ
Ophthalmic · 284d
Cleared Apr 19, 2022
QUATERA 700
K212241 · HQC
Ophthalmic · 274d
Cleared Jun 15, 2020
Visalis V500, Visalis S500
K193376 · HQC
Ophthalmic · 193d
Cleared Mar 06, 2019
VISULAS green
K181682 · HQF
Ophthalmic · 253d
Cleared Jan 11, 2019
RESCAN 700, CALLISTO eye
K180229 · OBO
Ophthalmic · 350d
Cleared Aug 24, 2018
IOLMaster 700
K173771 · HJO
Ophthalmic · 256d
Cleared Jun 27, 2018
CALLISTO eye
K180858 · NFJ
Ophthalmic · 86d
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