ClearanceBrief
Company ยท US

Kub Technologies, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 2007 to 2021. Name variants (Inc, Corp, punctuation) are merged.

10510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
MWPCabinet, X-Ray System6
MQBSolid State X-Ray Imager (Flat Panel/Digital Imager)2
IZLSystem, X-Ray, Mobile1
KPRSystem, X-Ray, Stationary1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 20, 2021K210955Kubtec Mozart Supra (XPERT 84) Radiography System
Kub Technologies, Inc.
MWP
Aug 31, 2021K210957Kubec Xpert 80 Radiography System
Kub Technologies, Inc.
MWP
Aug 31, 2021K210956Kubtec Mozart (XPERT42)
Kub Technologies, Inc.
MWP
Jun 12, 2020K200756Kubtec Mozart Supra
Kub Technologies, Inc.
MWP
Jun 20, 2019K183624Kubtec Mozart (Xpert42)
Kub Technologies, Inc.
MWP
Jun 23, 2015K151221Kubtec DIGIVIEW 395
Kub Technologies, Inc.
MQB
Oct 29, 2014K141539KUBTEC X250
Kub Technologies, Inc.
IZL
Oct 20, 2011K103348DIGIVIEW 250
Kub Technologies, Inc.
MQB
Jan 8, 2009K083510KUBTEC XPERT 20
Kub Technologies, Inc.
KPR
Jun 20, 2007K071233XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM
Kub Technologies, Inc.
MWP

Latest recalls

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