Medical Device Manufacturer · US , Oakland , CA

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

2 submissions · 2 cleared · Since 2021

Total

Cleared

Denied

Promaxo, Inc. has 2 FDA 510(k) cleared medical devices. Based in Oakland, US.

Last cleared in 2023. Active since 2021. Primary specialty: Radiology.

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

Promaxo, 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 - Promaxo, Inc.

2 devices

1-2 of 2