FDA Product Code EBI: Resin, Denture, Relining, Repairing, Rebasing
FDA product code EBI covers denture relining, repairing, and rebasing resins used to restore or modify the fit of existing dentures.
These acrylic resin materials are used to add new base material to a worn or ill-fitting denture — compensating for bone resorption that occurs after tooth extraction — or to repair fractures in existing prostheses. They are available for chairside or laboratory application.
EBI devices are Class II medical devices, regulated under 21 CFR 872.3760 and reviewed by the FDA Dental panel.
Leading manufacturers include Dentsply Intl., Dentsply Sirona and Sprintray, Inc..
330
Total
330
Cleared
105d
Avg days
1978
Since
330 devices
Cleared
Aug 12, 1988
TRIAD ORTHODONTIC GEL
Dentsply Intl.
Dental
57d
Cleared
Sep 05, 1986
TRIAD IMPACT
Dentsply Intl.
Dental
9d
Cleared
Feb 27, 1984
DENTURE BASE RESIN
Dentsply Intl.
Dental
75d
Cleared
Jun 30, 1983
DENTURE RELINING, REPAIR/REBASING RESIN
Dentsply Intl.
Dental
38d
Cleared
Mar 12, 1980
MAXUM DENTURE RESIN
Dentsply Intl.
Dental
15d
Cleared
Nov 30, 1979
DENTURE BASE RESIN
Dentsply Intl.
Dental
49d
Cleared
Jun 14, 1978
DENTURE RELINE MATERIAL
Dentsply Intl.
Dental
33d