Medical Device Manufacturer · JP , Chiyoda-Ku

Prexion Corporation - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 2016

Recent clearances: PreXion3D Expedition, PreXion3D Expedition, PreXion3D Explorer PRO

Total

Cleared

Denied

Prexion Corporation has 9 FDA 510(k) cleared medical devices. Based in Chiyoda-Ku, JP.

Last cleared in 2023. Active since 2016. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Prexion Corporation Filter by specialty or product code using the sidebar.

Prexion Corporation is one of 79 FDA 510(k) medical device manufacturers from Japan in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Prexion Corporation

9 devices

1-9 of 9

PreXion3D Explorer PRO

K221525 · OAS

Radiology · 57d

Cleared Feb 23, 2021

PreXion3D Explorer PRO

K203784 · OAS

Radiology · 57d

Cleared Apr 09, 2020

PreXion3D Explorer EX

Prexion Corporation - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Prexion Corporation

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