# K033045: Dream Bond, Dreamcast Chrome, Dreamcast V, Dream Flexicast, Dream Lithecast

- Pathway: 510(k) (Traditional)
- Applicant: American Green Dent. Mfg, Inc.
- Decided: Dec 23, 2003 after 85 days
- Product code: EJH (Alloy, Metal, Base)
- Device class: 2
- Regulation: 21 CFR 872.3710
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Indications for use
"DREAMBOND" (Ceramic dental casting Alloy) is used in dental laboratories, suitable for fabrication of metal-ceramic dental restorations. "DREAMCAST CHROME" (Partial Denture Dental Casting Alloy) is for the use in dental laboratories, suitable for preparation of removable dental applications. "DREAMCAST V" (Ceramic dental casting Alloy) is used in dental laboratories, suitable for fabrication of metal-ceramic dental restorations. "DREAM FLEXICAST" (Partial Denture Cobalt Base Alloy) is for the use in dental laboratories. suitable for preparation of removable dental applications. "DREAM LITHECAST" (Ceramic dental casting Alloy Nickel & Beryllium Free) is used in dental laboratories, suitable for fabrication of metal-ceramic dental restorations.

Source page: https://510kreport.com/device/K033045
Methodology: https://510kreport.com/methodology