Medical Device Manufacturer · US , Chicago , IL

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

1 submissions · 1 cleared · Since 2023

Total

Cleared

Denied

Retmap, Inc. has 1 FDA 510(k) cleared medical devices. Based in Chicago, US.

Last cleared in 2023. 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.

FDA 510(k) cleared devices by Retmap, Inc.

1 devices

1-1 of 1