# K000894: C&B Resin Plus Powder/Liquid, Models Retemp A2, A3, A3.5, CL, Retemp B2, B3, C2, D3, WH, Retemp MO

- Pathway: 510(k) (Traditional)
- Applicant: Dental Ventures of America, Inc.
- Decided: May 19, 2000 after 60 days
- Product code: EBG (Crown And Bridge, Temporary, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3770
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K103474: Ena Temp and Enamel Plus Temp (Two Different Proprietary Names for the Same Product) (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K000894
Methodology: https://510kreport.com/methodology