Prime Dental Manufacturing, Inc. is one of 20558 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Prime Dental Manufacturing, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PRIME-DENT DUAL CURE COMPOSITE LUTING CEMENT, PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL, LIGHT CURE DENTAL DAM
9
Total
9
Cleared
0
Denied
Prime Dental Manufacturing, Inc. has 9 FDA 510(k) cleared medical devices. Based in Chicago, US.
Historical record: 9 cleared submissions from 2000 to 2012. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Prime Dental Manufacturing, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Prime Dental Manufacturing, Inc.
9 devices
Cleared
Jan 23, 2012
PRIME-DENT DUAL CURE COMPOSITE LUTING CEMENT
Dental
139d
Cleared
Nov 07, 2002
PRIME-DENT AUTOMIX DUAL CURE CORE BUILD UP MATERIAL
Dental
87d
Cleared
Jul 19, 2002
LIGHT CURE DENTAL DAM
Dental
70d
Cleared
Feb 19, 2002
PRIME-DENT HEMA DESENSITIZER
Dental
78d
Cleared
Nov 05, 2001
PRIME-DENT CHEMICAL CURE PIT & FISSURE SEALANT
Dental
76d
Cleared
Nov 01, 2001
PRIME-DENT VISIBLE LIGHT CURE PIT & FISSURE SEALANT
Dental
76d
Cleared
Oct 24, 2001
PRIME-DENT ONE-STEP ORTHODONTIC ADHESIVE BONDING SYSTEM
Dental
71d
Cleared
May 30, 2000
PRIME-DENT VISIBLE LIGHT CURE COMPOSITE RESTORATIVE MATERIAL
Dental
55d
Cleared
Jan 31, 2000
PRIME-DENT CHEMICAL CURE COMPOSITE RESTORATIVE MATERIAL
Dental
47d