Retmap, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Retmap, Inc. - FDA 510(k) Cleared Devices
Recent clearances: RM Electrode (RMH 25-01), RM Electrode (RMH 23-01)
2
Total
2
Cleared
0
Denied
Retmap, Inc. has 2 FDA 510(k) cleared medical devices. Based in Chicago, US.
Latest FDA clearance: Apr 2026. Active since 2023. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Retmap, Inc. Filter by specialty or product code using the sidebar.
2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Retmap, Inc.
2 devices