Prosthetic devices · 21 CFR 872 Subpart D
Cement Dissolving Solution
FDA device type “Solution, Cement Dissolving”.
- Companies listing it
- 11 makers
- Brands and models
- 2
- 510(k) clearances
- 20 in five years
- FDA name
- Solution, Cement Dissolving
510(k) clearances per year, 1976–2026
Companies that list KZP
1 company currently list this device type with FDA.
| Company | Country | Role | Brands and models listed | Clearances | Latest |
|---|---|---|---|---|---|
| Den-Mat Holdings, LLC | United States | Maker | Dry-Bond · Solvenex | 8 | 2026 |
510(k) clearances
| Decided | 510(k) | Device | Applicant |
|---|---|---|---|
| 8 Apr 1993 | K920843 | TOOTH CONDITIONER | Confi-Dental Products Co. |
| 12 Jan 1978 | K771974 | SOLVENEX I-0 | Den-Mat Corp. |
Official records: FDA product classification for KZP · 21 CFR 872.3750.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026