Kub Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kub Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Kubtec Mozart Supra (XPERT 84) Radiography System, Kubtec Mozart (XPERT42), Kubec Xpert 80 Radiography System
10
Total
10
Cleared
0
Denied
Kub Technologies, Inc. has 10 FDA 510(k) cleared radiology devices. Based in Shelton, US.
Last cleared in 2021. Active since 2007.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kub Technologies, Inc.
10 devices
Cleared
Sep 20, 2021
Kubtec Mozart Supra (XPERT 84) Radiography System
Radiology
174d
Cleared
Aug 31, 2021
Kubtec Mozart (XPERT42)
Radiology
154d
Cleared
Aug 31, 2021
Kubec Xpert 80 Radiography System
Radiology
154d
Cleared
Jun 12, 2020
Kubtec Mozart Supra
Radiology
80d
Cleared
Jun 20, 2019
Kubtec Mozart (Xpert42)
Radiology
176d
Cleared
Jun 23, 2015
Kubtec DIGIVIEW 395
Radiology
47d
Cleared
Oct 29, 2014
KUBTEC X250
Radiology
141d
Cleared
Oct 20, 2011
DIGIVIEW 250
Radiology
339d
Cleared
Jan 08, 2009
KUBTEC XPERT 20
Radiology
43d
Cleared
Jun 20, 2007
XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM
Radiology
48d