Pulpdent Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulpdent Corp. - FDA 510(k) Cleared Devices
78
Total
78
Cleared
0
Denied
Pulpdent Corp. has 78 FDA 510(k) cleared dental devices. Based in Watertown, US.
Historical record: 78 cleared submissions from 1990 to 2002.
Browse the complete list of FDA 510(k) cleared dental devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pulpdent Corp.
78 devices
Cleared
Mar 14, 2002
PULPDENT NO-MIX ORTHODONTIC BRACKET ADHESIVE
Dental
87d
Cleared
Mar 14, 2002
PULPDENT TRIPLE-CURE REINFORCED GLASS IONOMER ORTHODONTIC CEMENT
Dental
87d
Cleared
Feb 28, 2002
PULPDENT SEALANT/PASTE ORTHODONTIC BRACKET ADHESIVE SYSTEM
Dental
48d
Cleared
Feb 27, 2002
PULPDENT TRANS OBA ORTHODONTIC BRACKET ADHESIVE
Dental
79d
Cleared
Dec 12, 2001
PULPDENT CAVITY PREPARATION IV
Dental
58d
Cleared
Mar 02, 2000
PULPDENT CAVITY PREPARATION III
Dental
83d
Cleared
Feb 29, 2000
PULPDENT CAVITY PREPARATION II, PULPDENT CAVITY PREPARATION II WUTH FLUORIDE
Dental
81d
Cleared
Feb 23, 2000
PULPDENT CAVITY PREPARATION 1, PULPDENT CAVITY PREPARATION 1 WITH FLUORIDE
Dental
75d
Cleared
Dec 13, 1999
PULPDENT UNO-DUO
Dental
42d
Cleared
Mar 19, 1998
PULPDENT CAVITY CLEANSER, PULPDENT CAVITY CLEANSER PLUS
Dental
129d
Cleared
Feb 18, 1998
PULPDENT CAVITY VARNISH
Dental
89d
Cleared
Dec 17, 1997
PULPDENT DENTASTIC UNO
Dental
56d
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