Gendex Corp. - FDA 510(k) Cleared Devices
14
Total
14
Cleared
0
Denied
Gendex Corp. has 14 FDA 510(k) cleared radiology devices. Based in Mchenry, US.
Historical record: 14 cleared submissions from 1984 to 1995.
Browse the complete list of FDA 510(k) cleared radiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
14 devices
Cleared
Jun 29, 1995
GX-PAN PANORAMIC DENTAL X-RAY SYSTEM
Radiology
23d
Cleared
Feb 09, 1995
PROCESSOR, RADIOGRAPHIC-FILM, AUTOMATIC, DENTAL
Radiology
80d
Cleared
Feb 18, 1994
GX-770 X-RAY CONTROL, MODEL 46-404600G4
Radiology
121d
Cleared
Sep 29, 1993
VISUALIX RADIOGRAPHIC IMAGE DETECTING AND PROCESS
Radiology
357d
Cleared
Sep 14, 1993
ORALIX DC
Radiology
200d
Cleared
Jul 26, 1993
GXP DENTAL X-RAY PROCESSOR
Radiology
54d
Cleared
Jul 27, 1992
ATC725, ATC525, AND AP300
Radiology
80d
Cleared
Apr 28, 1992
GX-C CEPHALOMETER
Radiology
104d
Cleared
Oct 03, 1989
GX-ELEVATOR
Radiology
109d
Cleared
Mar 31, 1989
GX-2000 STATIONARY X-RAY GENERATOR
Radiology
80d
Cleared
Oct 30, 1987
GX-MOBILE X-RAY UNIT
Radiology
30d
Cleared
Apr 22, 1986
GENDEX PRINCE 30 MEDICAL X-RAY GENERATOR
Radiology
161d