Medical Device Manufacturer · US , Minneapolis , MN

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

3 submissions · 3 cleared · Since 2023

Total

Cleared

Denied

Imbio, Inc. has 3 FDA 510(k) cleared medical devices. Based in Minneapolis, US.

Latest FDA clearance: Dec 2024. Active since 2023. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Imbio, Inc. Filter by specialty or product code using the sidebar.

Imbio, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Imbio, Inc.

3 devices

1-3 of 3