Minxray, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Minxray, Inc. - FDA 510(k) Cleared Devices
Recent clearances: IMPACT and X-Ranger, CMDR 2C (Multiple Models), CMDR 2CW (Multiple models)
18
Total
18
Cleared
0
Denied
Minxray, Inc. has 18 FDA 510(k) cleared radiology devices. Based in Mchenry, US.
Last cleared in 2021. Active since 1976.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Minxray, Inc.
18 devices
Cleared
Mar 19, 2021
IMPACT and X-Ranger
Radiology
28d
Cleared
Jul 08, 2020
CMDR 2C (Multiple Models)
Radiology
27d
Cleared
Jul 03, 2019
CMDR 2CW (Multiple models)
Radiology
33d
Cleared
Dec 14, 2018
TR90BH
Radiology
121d
Cleared
Jun 07, 2017
CMDR 2ST (Multiple Models), CMDR 2SPE (Multiple Models), Integris
Radiology
29d
Cleared
Feb 02, 2016
HF1202H PowerPlus Portable X-ray Equipment
Radiology
104d
Cleared
Sep 18, 2014
CMDR-2ST & CMDR-2SLWT DIGITAL PORTABLE X-RAY
Radiology
69d
Cleared
May 12, 2010
MINXRAY, MODEL: BPD60
Radiology
378d
Cleared
Apr 23, 2010
MINXRAY MODEL CMDR-2S
Radiology
65d
Cleared
Nov 07, 2008
MINXRAY, MODEL CMDR-1S AND CMDR-1S-MIL
Radiology
59d
Cleared
Oct 27, 2005
MINXRAY, MODEL HF100H+
Radiology
28d
Cleared
Feb 02, 2004
MINXRAY, MODEL HF120/60H POWERPLUS
Radiology
21d