Prosthetic devices · 21 CFR 872 Subpart D
Mercury
FDA device type “Mercury”.
- Companies listing it
- 83 makers
- Brands and models
- 9
- 510(k) clearances
- 40 in five years
- FDA name
- Mercury
510(k) clearances per year, 1976–2026
Companies that list ELY
8 companies currently list this device type with FDA.
| Company | Country | Role | Brands and models listed | Clearances | Latest |
|---|---|---|---|---|---|
| Sybron Dental Specialties | United States | Maker | Tytin | 203 | 2026 |
| Sdi Limited | Australia | Maker | Ultracaps S | 8 | 2022 |
| New Stetic, SA | Colombia | Maker | Micronic · NU Alloy DP · Nu Alloy DP Active | 5 | 2026 |
| Jersey Dental Supplies | United States | Repacker / relabeler | NEW STETIC DENTAL AMALGAM ALLOY · TYTIN | — | — |
| Samtrade Supplies Inc. | Canada | Foreign exporter | Tytin Amalgam | — | — |
| Caribbean Dental Products Corp. | United States | Repacker / relabeler | AMALGAM | — | — |
| Mainline Medical Dental Supply | Canada | Foreign exporter | — | — | — |
| Oketz Logistics LLC | United States | Repacker / relabeler | — | — | — |
510(k) clearances
| Decided | 510(k) | Device | Applicant |
|---|---|---|---|
| 21 Jan 2010 | K093587 | DENTAL MERCURY | Dmg USA, Inc. |
| 23 Mar 1998 | K973548 | MERCURY DENTAL | Aleaciones Dentales Zeyco, S.A. DE C.V. |
| 16 Jan 1992 | K913814 | MODEL #05 ANEROID SPHYGMOMANOMETER KIT | National Health-Care Equipment, Inc. |
| 28 Jun 1990 | K902388 | DENTAL-QUECKSILBER (DENTAL MERCURY) | Degussa AG |
Official records: FDA product classification for ELY · 21 CFR 872.3070.
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026