Not currently registered with FDA under this name
Dental Alloy Products, Inc.
Compton, CA, United States. Named as applicant on 5 dental 510(k) clearances between 2000 and 2000. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 52000–2000
- Markets registered in
- 32 registrations outside the US
- Establishments
- 0—
510(k) clearances per year, 2000–2026
Registered in 3 markets
Where regulators' registries name Dental Alloy Products, 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 | Applicant | Dental Alloy Products, Inc. | 5 clearances | 2000–2000 | Below |
| Brazil | ANVISA | Manufacturer | DENTAL ALLOY PRODUCTS | 1 | 2011–2011 | Pure Global AI |
| Taiwan | TFDA | Manufacturer | Dental Alloy Products | 1 | 2015–2015 | 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
510(k) clearances
Clearances on which FDA names Dental Alloy Products, Inc. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 26 Sep 2000 | K002302 | SUPER 14 | EJH Base Metal Alloy |
| 26 Sep 2000 | K002300 | SUPER 6 | EJH Base Metal Alloy |
| 8 Sep 2000 | K002301 | SUPER 12 | EJH Base Metal Alloy |
| 8 Sep 2000 | K002299 | SUPER 3 | EJH Base Metal Alloy |
| 24 Aug 2000 | K002298 | SUPER 1 | EJH Base Metal Alloy |
Some of these clearances are listed with FDA today by another company: The Argen Corporation (1).
Sources
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 of the most recent filing, which can be a US agent.