# K955292: Aeliteflo

- Pathway: 510(k) (Traditional)
- Applicant: Bisco, Inc.
- Decided: Dec 13, 1995 after 26 days
- Product code: EBF (Material, Tooth Shade, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3690
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
19 later devices descend from it; 4 cite it directly.
0 of 20 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K981965: Flowable Composite (1998), 11 descendants of its own
- K083841: Adaptable Composite Resin Restorative Material (2009), 9 descendants of its own
- K120453: Filtek Bulk Fill Flowable Restorative (2012), 8 descendants of its own
- K982395: Dytract Flow Restorative (1998), 3 descendants of its own
- K182714: Novidia Bulk Fill Flow Composite (2019), 2 descendants of its own

Source page: https://510kreport.com/device/K955292
Methodology: https://510kreport.com/methodology