Medical Device Manufacturer · US , Watertown , MA

Pulpdent Corp. - FDA 510(k) Cleared Devices

78 submissions · 78 cleared · Since 1990

Recent clearances: PULPDENT NO-MIX ORTHODONTIC BRACKET ADHESIVE, PULPDENT TRIPLE-CURE REINFORCED GLASS IONOMER ORTHODONTIC CEMENT, PULPDENT SEALANT/PASTE ORTHODONTIC BRACKET ADHESIVE SYSTEM

78

Total

78

Cleared

0

Denied

FDA 510(k) Regulatory Record - Pulpdent Corp. Dental ✕

78 devices

1-12 of 78

Cleared Mar 14, 2002

PULPDENT NO-MIX ORTHODONTIC BRACKET ADHESIVE

Cleared Mar 14, 2002

PULPDENT TRIPLE-CURE REINFORCED GLASS IONOMER ORTHODONTIC CEMENT

Cleared Feb 28, 2002

PULPDENT SEALANT/PASTE ORTHODONTIC BRACKET ADHESIVE SYSTEM

Cleared Feb 27, 2002

PULPDENT TRANS OBA ORTHODONTIC BRACKET ADHESIVE

Cleared Dec 12, 2001

PULPDENT CAVITY PREPARATION IV

Cleared Mar 02, 2000

PULPDENT CAVITY PREPARATION III

Cleared Feb 29, 2000

PULPDENT CAVITY PREPARATION II, PULPDENT CAVITY PREPARATION II WUTH FLUORIDE

Cleared Feb 23, 2000

PULPDENT CAVITY PREPARATION 1, PULPDENT CAVITY PREPARATION 1 WITH FLUORIDE

Cleared Dec 13, 1999

PULPDENT UNO-DUO

Cleared Mar 19, 1998

PULPDENT CAVITY CLEANSER, PULPDENT CAVITY CLEANSER PLUS

Cleared Feb 18, 1998

PULPDENT CAVITY VARNISH

Cleared Dec 17, 1997

PULPDENT DENTASTIC UNO

Looking for a specific device from Pulpdent Corp.? Search by device name or K-number.

Search all Pulpdent Corp. devices