EBI · Class II · 21 CFR 872.3760

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 Prismatik Dentalcraft, Inc., Keystone Industries and Voco GmbH.

328
Total
328
Cleared
105d
Avg days
1978
Since
328 devices
217–240 of 328
No devices found for this product code.