Kub Technologies, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
10
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K210955Kubtec Mozart Supra (XPERT 84) Radiography SystemSeptember 20, 2021
K210956Kubtec Mozart (XPERT42)August 31, 2021
K210957Kubec Xpert 80 Radiography SystemAugust 31, 2021
K200756Kubtec Mozart SupraJune 12, 2020
K183624Kubtec Mozart (Xpert42)June 20, 2019
K151221Kubtec DIGIVIEW 395June 23, 2015
K141539KUBTEC X250October 29, 2014
K103348DIGIVIEW 250October 20, 2011
K083510KUBTEC XPERT 20January 8, 2009
K071233XPERT 40 SPECIMEN RADIOGRAPHY SYSTEMJune 20, 2007