Medical Device Manufacturer · US , Chicago , IL

Retmap, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2023
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Retmap, Inc. Ophthalmic ✕
2 devices
1-2 of 2
Cleared CT Apr 01, 2026
RM Electrode (RMH 25-01)
K253586 · HLZ
Ophthalmic · 135d
Cleared CT Dec 07, 2023
RM Electrode (RMH 23-01)
K232273 · HLZ
Ophthalmic · 129d
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