Miscellaneous devices · 21 CFR 872 Subpart G
Silicate Protector
FDA device type “Protector, Silicate”.
- Companies listing it
- 118 makers
- Brands and models
- 5
- 510(k) clearances
- 00 in five years
- FDA name
- Protector, Silicate
Companies that list EFX
11 companies currently list this device type with FDA.
| Company | Country | Role | Brands and models listed | Clearances | Latest |
|---|---|---|---|---|---|
| GC America Inc. | United States | Maker | StickREFIX | 137 | 2026 |
| Zest Anchors, LLC | United States | Maker | — | 26 | 2026 |
| Vita Zahnfabrik H. Rauter GmbH & Co. Kg. | Germany | Maker | VITAFol H | 8 | 2026 |
| Keystone Industries | United States | Maker | Masque Silicone Lubricant & Separator | 2 | 2025 |
| bredent GmbH & Co. KG | Germany | Maker | — | 3 | 2024 |
| Nawaz and Sons | Pakistan | Maker | EFX / PROTECTOR, SILICATE | — | — |
| MG Development America Inc. | United States | Maker | — | — | — |
| MG Developpement | France | Maker | — | — | — |
| Parkell, Inc | United States | Contract manufacturer | — | 58 | 2025 |
| Dentimed Sao Joao LLC | United States | Repacker / relabeler | TOSCANA | — | — |
| Sanicure BV | Netherlands | Foreign exporter | — | — | — |
Official records: FDA product classification for EFX · 21 CFR 872.6670.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026