Manufacturer registered with FDA
E. C. Moore Company, Inc.
Dearborn, MI, United States. Lists 5 dental device types with FDA across 1 registered establishment, and holds 1 510(k) clearance as applicant.
- Device types listed
- 5
- Brands and models
- 5
- 510(k) clearances
- 11979–1979
- Markets registered in
- 34 registrations outside the US
- Establishments
- 1United States
510(k) clearances per year, 1976–2026
Registered in 3 markets
Where regulators' registries name E. C. Moore Company, Inc. as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | E. C. Moore Company, Inc. | 1 clearances | 1979–1979 | Below |
| Australia | TGA | Manufacturer | E C Moore Co | 2 | 2009–2019 | Pure Global AI |
| South Korea | MFDS | Manufacturer | E.C. Moore Company, Inc.E.C.Moore Company, Inc. | 2 | 2001–2014 | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What E. C. Moore Company, Inc. currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Abrasive DiskEHJ · Class 1 | Polishing & prophylaxis | Maker | E.C. Moore; Cosmedenr | 2010 |
| Abrasive PointEHL · Class 1 | Polishing & prophylaxis | Maker | E.C. Moore | 2013 |
| Polishing Agent StripEHM · Class 1 | Polishing & prophylaxis | Maker | E.C. Moore; Cosmedent | 2013 |
| Dental BurEJL · Class 1 | Dental burs & diamonds | Maker | E.C. Moore | 2013 |
| Oral Cavity Abrasive Polishing AgentEJR · Class 1 | Polishing & prophylaxis | Maker | PopWhite Prophy Paste | 2010 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| E. C. MOORE COMPANY, INC.FDA reg. 1824299 | Dearborn, MI, United States | Manufacturer |
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10031306). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.