Not currently registered with FDA under this name
Aurex Precious Metal Industries (Pty)Ltd
Edenvale, South Africa. Named as applicant on 19 dental 510(k) clearances between 1997 and 1997. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 191997–1997
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Aurex Precious Metal Industries (Pty)Ltd as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 19 Dec 1997 | K972946 | AURELUX 77 | EJT Gold-Based Noble Metal Alloy |
| 26 Nov 1997 | K972945 | AURENORM 68 | EJS Alloy Other Noble Metal |
| 18 Sep 1997 | K972949 | AURELUX BIO Y85PF | EJT Gold-Based Noble Metal Alloy |
| 16 Sep 1997 | K972943 | AURECAST 92 | EJT Gold-Based Noble Metal Alloy |
| 5 Sep 1997 | K972956 | PALCERAM 82SF | EJT Gold-Based Noble Metal Alloy |
| 5 Sep 1997 | K972955 | PALCERAM 56 | EJT Gold-Based Noble Metal Alloy |
| 5 Sep 1997 | K972954 | PALAUREX 78 | EJT Gold-Based Noble Metal Alloy |
| 5 Sep 1997 | K972953 | PALAUREX 76KF | EJT Gold-Based Noble Metal Alloy |
| 5 Sep 1997 | K972952 | AUREBOND 51 | EJT Gold-Based Noble Metal Alloy |
| 5 Sep 1997 | K972951 | HIPALLAUR 51 | EJT Gold-Based Noble Metal Alloy |
| 5 Sep 1997 | K972950 | HIPALLAUR 19 | EJT Gold-Based Noble Metal Alloy |
| 28 Aug 1997 | K972942 | AURECAST 83 | EJT Gold-Based Noble Metal Alloy |
| 28 Aug 1997 | K972941 | AURECAST 74 | EJT Gold-Based Noble Metal Alloy |
| 26 Aug 1997 | K972940 | AURECAST BIO 69PF | EJT Gold-Based Noble Metal Alloy |
| 26 Aug 1997 | K972939 | AURECAST BIO 59PF | EJT Gold-Based Noble Metal Alloy |
| 26 Aug 1997 | K972319 | AURECAST GF | EJT Gold-Based Noble Metal Alloy |
| 25 Aug 1997 | K972938 | AURECAST 10 | EJT Gold-Based Noble Metal Alloy |
| 25 Aug 1997 | K972937 | AURECAST 4 | EJT Gold-Based Noble Metal Alloy |
| 25 Aug 1997 | K972936 | AURECAST 2 | EJT Gold-Based Noble Metal Alloy |
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.