Pulpdent Corp. of America is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulpdent Corp. of America - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Pulpdent Corp. of America has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1981 to 1988. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Pulpdent Corp. of America Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pulpdent Corp. of America
6 devices
Cleared
Jul 15, 1988
ACID ETCH GEL
Dental
23d
Cleared
Feb 06, 1987
EVIDENT MARK 2 APEX LOCATOR
Dental
129d
Cleared
Feb 20, 1986
FIBER MESH
Dental
70d
Cleared
Oct 29, 1985
BISICO SL(PUTTY) BISICO S2(REGULAR) S3 HEAVY ETC.
Dental
347d
Cleared
Oct 16, 1985
POLYCARB WATER SET
Dental
61d
Cleared
Mar 24, 1981
PCA PERIOCARE PERIODONTAL DRESSING
Dental
25d