Medical Device Manufacturer · DE , Wetzlar

Oculus Optikger?te GmbH - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2021
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Oculus Optikger?te GmbH Ophthalmic ✕
2 devices
1-2 of 2
Cleared Mar 13, 2026
Pentacam® Cornea OCT
K251848 · MXK
Ophthalmic · 270d
Cleared Jul 14, 2021
Myopia Master
K202989 · MXK
Ophthalmic · 287d
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