Not currently registered with FDA under this name
Alpha-Dent
Chicago, IL, United States. Named as applicant on 6 dental 510(k) clearances between 1991 and 1994. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 61991–1994
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 1990–2026
510(k) clearances
Clearances on which FDA names Alpha-Dent as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 3 Feb 1994 | K932828 | CENTRIX'S ENCORE SOLO LIGHT ACTIVATED RESIN CORE | EBF Resin Tooth Shade Material |
| 28 Jan 1994 | K932829 | CENTRIX'S ENCORE NATURAL COMPOSITE RESIN CORE PAST | EBF Resin Tooth Shade Material |
| 28 Jan 1994 | K932826 | CENTRIX'S ENCORE COMPOSITE RESIN CORE PASTE W\FLUO | EBF Resin Tooth Shade Material |
| 23 Sep 1993 | K932827 | ALPHA-DENT CORE BUILDUP PASTE | EBF Resin Tooth Shade Material |
| 31 May 1991 | K904813 | VISIBLE LIGHT CURE COMPOSITE DENTAL RESTOR. MAT. | EBF Resin Tooth Shade Material |
| 26 Feb 1991 | K904812 | COMPOSITE RESTORATIVE MATERIAL/RADIOPAQUE | EBF Resin Tooth Shade Material |
Some of these clearances are listed with FDA today by another company: Dental Technologies, Inc. (3), Centrix, Inc. (2).
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.