ELY
4 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Mercury
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 872.3070
- Medical specialty
- Dental
- Flags
- Third-party review eligible
- Adverse events (MAUDE)
- 1998: 1 · 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 |
|---|---|---|
| DENTAL MERCURY (K093587) | Dmg USA, Inc. | 2010-01-21 |
| MERCURY DENTAL (K973548) | Aleaciones Dentales Zeyco, S.A. DE C.V. | 1998-03-23 |
| MODEL #05 ANEROID SPHYGMOMANOMETER KIT (K913814) | National Health-Care Equipment, Inc. | 1992-01-16 |
| DENTAL-QUECKSILBER (DENTAL MERCURY) (K902388) | Degussa AG | 1990-06-28 |
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Every clearance here is in the API, with alerts when new ones post.