Prosthetic devices · 21 CFR 872 Subpart D
Carboxymethylcellulose Sodium and Cationic Polyacrylamide Polymer Denture Adhesive
FDA device type “Adhesive, Denture, Carboxymethylcellulose Sodium And Cationic Polyacrylamide Polymer”.
- Companies listing it
- 00 makers
- Brands and models
- 0
- 510(k) clearances
- 00 in five years
- FDA name
- Adhesive, Denture, Carboxymethylcellulose Sodium And Cationic Polyacrylamide Polymer
Official records: FDA product classification for KOS · 21 CFR 872.3420.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026