FDA Product Code KLE: Agent, Tooth Bonding, Resin
FDA product code KLE covers resin-based dental bonding agents used to bond composite restorations and porcelain veneers to tooth structure.
These multi-step or all-in-one adhesive systems create a micromechanical and chemical bond between the dentin/enamel substrate and the restorative material. They are an essential component of modern adhesive dentistry and direct composite restoration.
KLE devices are Class II medical devices, regulated under 21 CFR 872.3200 and reviewed by the FDA Dental panel.
Leading manufacturers include Dentsply Intl., Ultradent Products, Inc. and Bisco, Inc..
419
Total
419
Cleared
84d
Avg days
1976
Since
419 devices
Cleared
Mar 17, 1983
MICRODAPT DENTAL RESTORATIVE BONDING
Johnson & Johnson Professionals, Inc.
Dental
41d
Cleared
Sep 07, 1982
AURAFILL* DENTAL RESTORATIVE BONDING AG.
Johnson & Johnson Professionals, Inc.
Dental
22d
Cleared
Jan 12, 1982
SCOTCHBOND DENTAL ADHESIVE
3M Company
Dental
61d
Cleared
Nov 12, 1980
INSTANT BRIDGE
Scientific Pharmaceuticals, Inc.
Dental
50d
Cleared
May 20, 1980
PRISMA-BOND
Dentsply Intl.
Dental
12d
Cleared
Apr 30, 1979
VISIO-BOND
Espe GmbH (Us)
Dental
Cleared
Aug 03, 1977
UVIOBOND
Espe GmbH (Us)
Dental
16d
Cleared
Aug 02, 1977
NIMETIC ETCHING GEL
Espe GmbH (Us)
Dental
15d
Cleared
Aug 02, 1977
NIMETIC BONDING MATERIAL
Espe GmbH (Us)
Dental
15d