Alpha-Dent is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Alpha-Dent - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Alpha-Dent has 6 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 6 cleared submissions from 1991 to 1994. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Alpha-Dent Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Alpha-Dent
6 devices
Cleared
Feb 03, 1994
CENTRIX'S ENCORE SOLO LIGHT ACTIVATED RESIN CORE
Dental
239d
Cleared
Jan 28, 1994
CENTRIX'S ENCORE COMPOSITE RESIN CORE PASTE W\FLUO
Dental
233d
Cleared
Jan 28, 1994
CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST
Dental
233d
Cleared
Sep 23, 1993
ALPHA-DENT CORE BUILDUP PASTE
Dental
106d
Cleared
May 31, 1991
VISIBLE LIGHT CURE COMPOSITE DENTAL RESTOR. MAT.
Dental
218d
Cleared
Feb 26, 1991
COMPOSITE RESTORATIVE MATERIAL/RADIOPAQUE
Dental
124d