Diagnostic devices · 21 CFR 872 Subpart B
Electrode Gel for Pulp Tester
FDA device type “Gel, Electrode, For Pulp Tester”.
- Companies listing it
- 20 makers
- Brands and models
- 2
- 510(k) clearances
- 00 in five years
- FDA name
- Gel, Electrode, For Pulp Tester
Companies that list EAS
2 companies currently list this device type with FDA.
| Company | Country | Role | Brands and models listed | Clearances | Latest |
|---|---|---|---|---|---|
| Dentimed Sao Joao LLC | United States | Repacker / relabeler | TOSCANO | — | — |
| Dongguan Yingfeng Metal & Plastic Products Co., Ltd | China | Foreign exporter | Conductive Gel for external use | — | — |
Official records: FDA product classification for EAS · 21 CFR 872.1730.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026