ClearanceBrief
Company ยท JP

Prexion Corporation

FDA 510(k) clearances and medical device recalls filed under this name, 2016 to 2023. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
OASX-Ray, Tomography, Computed, Dental9

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 8, 2023K232166PreXion3D Expedition
Prexion Corporation, JP
OAS
Jan 12, 2023K222150PreXion3D Expedition
Prexion Corporation, JP
OAS
Jul 22, 2022K221525PreXion3D Explorer PRO
Prexion Corporation, JP
OAS
Feb 23, 2021K203784PreXion3D Explorer PRO
Prexion Corporation, JP
OAS
Apr 9, 2020K193329PreXion3D Explorer EX
Prexion Corporation, JP
OAS
Apr 15, 2019K190320PreXion3D Explorer
Prexion Corporation, JP
OAS
Aug 17, 2018K181983PreXion 3D Excelsior
Prexion Corporation, JP
OAS
Jan 19, 2018K173878PreXion3D Excelsior
Prexion Corporation, JP
OAS
Oct 3, 2016K161881PreXion3D Excelsior
Prexion Corporation, JP
OAS

Latest recalls

DateFirm and productCodeLinked 510(k)
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