Ortho Source is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ortho Source - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Ortho Source has 9 FDA 510(k) cleared medical devices. Based in North Hollywood, US.
Historical record: 9 cleared submissions from 1986 to 1992. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ortho Source Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Ortho Source
9 devices
Cleared
Aug 27, 1992
FISSURE SEALER
Dental
366d
Cleared
Jan 14, 1992
ORTHO LIGHT CURE
Dental
140d
Cleared
Nov 19, 1991
SUMO GLASS IONOMER CEMENT
Dental
104d
Cleared
Feb 23, 1989
VISIBLE LIGHT CURE CALCIUM HYDROXIDE LINER
Dental
90d
Cleared
Jan 03, 1989
MAXIBOND
Dental
63d
Cleared
May 02, 1986
ORTHOJOIN, ORTHODONTIC ADHESIVE
Dental
38d
Cleared
Apr 17, 1986
PERMABAND (ORTHODONTIC ADHESIVE)
Dental
14d
Cleared
Apr 11, 1986
ORTHOSOURCE ETCH SYSTEMS
Dental
9d
Cleared
Mar 25, 1986
DEPENDABOND
Dental
12d