Discus Dental, Inc. is one of 21617 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Discus Dental, Inc. - FDA 510(k) Cleared Devices
Recent clearances: FLASHLITE REBEL*, RELIEF ACP ORAL CARE GEL, SPLASH! IMPRESSION MATERIAL DEVICE
10
Total
10
Cleared
0
Denied
Discus Dental, Inc. has 10 FDA 510(k) cleared dental devices. Based in Culver City, US.
Historical record: 10 cleared submissions from 2002 to 2007.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by California Department of Health Services and Underwriters Laboratories, Inc..
FDA 510(k) Regulatory Record - Discus Dental, Inc.
10 devices
Cleared
Dec 20, 2007
FLASHLITE REBEL*
Dental
6d
Cleared
Jan 10, 2007
RELIEF ACP ORAL CARE GEL
Dental
163d
Cleared
Aug 05, 2005
SPLASH! IMPRESSION MATERIAL DEVICE
Dental
3d
Cleared
Jul 13, 2005
PROTEGE ULTRASONIC INSERT
Dental
12d
Cleared
Jun 18, 2004
PROACTIVE CARE PROPHYLAXIS PASTE WITH FLUORIDE
Dental
197d
Cleared
Mar 25, 2004
PRECISION VPS IMPRESSION MATERIAL
Dental
73d
Cleared
Jan 27, 2004
DISCHEM CHEMICAL PROPORTIONING & DISPENSING SYSTEM FOR USE WITH CETYLCIDE-G...
General Hospital
97d
Cleared
May 09, 2003
MEGA BITE REGISTRATION - DENTAL BITE REGISTRATION MATERIAL
Dental
59d
Cleared
Jan 17, 2003
FLASH-LITE II LED DENTAL CURING LIGHT
Dental
70d
Cleared
Aug 20, 2002
FLASH-LITE LED DENTAL CURING LIGHT
Dental
48d