Schick Technologies, Inc. is one of 20446 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Schick Technologies, Inc. - FDA 510(k) Cleared Devices
Recent clearances: COMPUTED DENTAL RADIOGRAPHY, MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM, SCHICK COMPUTED ORAL RADIOLOGY SYSTEM
13
Total
13
Cleared
0
Denied
Schick Technologies, Inc. has 13 FDA 510(k) cleared radiology devices. Based in Sound Beach, US.
Historical record: 13 cleared submissions from 1994 to 2011.
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 Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Schick Technologies, Inc.
13 devices
Cleared
Apr 20, 2011
COMPUTED DENTAL RADIOGRAPHY
Radiology
33d
Cleared
Nov 30, 2009
MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM
Radiology
25d
Cleared
Nov 02, 2007
SCHICK COMPUTED ORAL RADIOLOGY SYSTEM
Radiology
92d
Cleared
Feb 17, 2006
CEPH, MODEL 4900
Radiology
58d
Cleared
Jun 07, 2004
MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM
Radiology
13d
Cleared
May 05, 2003
CDR PANX, MODEL 4792
Radiology
12d
Cleared
Oct 02, 2002
MODIFICATION TO COMPUTED ORAL RADIOLOGY SYSTEM
Radiology
27d
Cleared
May 26, 2000
MODIFICATION TO ACCUDEXA BONE DENSITOMETER
Radiology
21d
Cleared
Dec 11, 1998
CDR - PAN MODEL 4700
Radiology
134d
Cleared
Jun 04, 1998
ACCUDEXA BONE DENSITOMETER
Radiology
69d
Cleared
Dec 02, 1997
ACCUDEXA BONE DENSITOMETER
Radiology
204d
Cleared
Nov 22, 1996
CDR-CAM
Dental
63d
Cleared
Jan 31, 1994
COMPUTED ORAL RADIOLOGY SYSTEM
Radiology
201d