ClearanceBrief
Company ยท BE

Icometrix NV

FDA 510(k) clearances and medical device recalls filed under this name, 2016 to 2024. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
LLZSystem, Image Processing, Radiological5
QBSRadiological Computer Assisted Detection/Diagnosis Software For Fracture1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Nov 7, 2024K240712icobrain aria
Icometrix NV, BE
QBS
Feb 28, 2020K192962icobrain-ctp
Icometrix NV, BE
LLZ
Dec 13, 2019K192130Icobrain
Icometrix NV, BE
LLZ
Nov 6, 2018K181939icobrain
Icometrix NV, BE
LLZ
Mar 8, 2018K180326icobrain
Icometrix, BE
LLZ
Aug 9, 2016K161148icobrain
Icometrix, BE
LLZ

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
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