Prosthetic devices · 21 CFR 872 Subpart D
Carboxymethylcellulose Sodium (49%) and Ethylene-Oxide Homopolymer Denture Adhesive
FDA device type “Adhesive, Denture, Carboxymethylcellulose Sodium (49%) And Ethylene-Oxide Homopolymer”.
- Companies listing it
- 21 makers
- Brands and models
- 1
- 510(k) clearances
- 00 in five years
- FDA name
- Adhesive, Denture, Carboxymethylcellulose Sodium (49%) And Ethylene-Oxide Homopolymer
Companies that list KXW
2 companies currently list this device type with FDA.
| Company | Country | Role | Brands and models listed | Clearances | Latest |
|---|---|---|---|---|---|
| Fuzhou Rick Brown Biomaterials Co. Ltd. | China | Maker | — | 1 | 2023 |
| Dentimed Sao Joao LLC | United States | Repacker / relabeler | TOSCANA | — | — |
Official records: FDA product classification for KXW · 21 CFR 872.3410.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026