EHE
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Dispenser, Mercury And/Or Alloy
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 872.3080
- Medical specialty
- Dental
- Adverse events (MAUDE)
- 1999: 1
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| AMALGAM DISPENSER (K771749) | New Dimensions IN Medicine, Inc. | 1977-09-28 |
| DISPENSER, MERCURY & TABLET/POWDER (K771396) | Johnson & Johnson Professionals, Inc. | 1977-08-03 |
Track EHE automatically
Every clearance here is in the API, with alerts when new ones post.