# Alpha-Dent

- Location (FDA's records): Chicago, IL
- FDA decisions: 6 (1991–1994): 6 510(k) clearances
- Product codes: EBF (6)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Dmg USA, Inc.: 1 (https://510kreport.com/company/dmg-usa)

## Its most-cited devices
- K932826: Centrix's Encore Composite Resin Core Paste W\Fluo (1994), cited by 1

## Recent decisions
- K932828: Centrix's Encore Solo Light Activated Resin Core (Feb 3, 1994)
- K932826: Centrix's Encore Composite Resin Core Paste W\Fluo (Jan 28, 1994)
- K932829: Centrix's Encore Natural Composite Resin Core Past (Jan 28, 1994)
- K932827: Alpha-Dent Core Buildup Paste (Sep 23, 1993)
- K904813: Visible Light Cure Composite Dental Restor. Mat. (May 31, 1991)
- K904812: Composite Restorative Material/Radiopaque (Feb 26, 1991)

Source page: https://510kreport.com/company/alpha-dent