EFX — Protector, Silicate Class I

FDA Device Classification

FDA product code EFX covers "Protector, Silicate", a Class I medical device regulated under 21 CFR 872.6670. Submissions are reviewed by the Dental panel.

Classification Details

Product Code
EFX
Device Class
Class I
Regulation Number
872.6670
Submission Type
Review Panel
DE
Medical Specialty
Dental
Implant
No