Not currently registered with FDA under this name
Bego U.S.A.
Lincoln, RI, United States. Named as applicant on 7 dental 510(k) clearances between 1998 and 2004. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 71998–2004
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Bego U.S.A. as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 15 Jan 2004 | K033279 | GOLD DENTAL CASTING ALLOYS | EJT Gold-Based Noble Metal Alloy |
| 4 Sep 2003 | K032136 | WIROBOND C | EJH Base Metal Alloy |
| 28 Oct 1998 | K983082 | BEGOCER G | EJT Gold-Based Noble Metal Alloy |
| 28 Oct 1998 | K983080 | AUROLLOYD KF | EJT Gold-Based Noble Metal Alloy |
| 23 Oct 1998 | K983079 | PLATINLLOYD 100 | EJT Gold-Based Noble Metal Alloy |
| 23 Oct 1998 | K983078 | BEGOPAL | EJS Alloy Other Noble Metal |
| 23 Oct 1998 | K983077 | BIO PONTOSTAR | EJT Gold-Based Noble Metal Alloy |
Some of these clearances are listed with FDA today by another company: Pan-Am Dental, Inc. (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.