# K092384: Liquicord

- Pathway: 510(k) (Traditional)
- Applicant: Centrix, Inc.
- Decided: Nov 4, 2009 after 91 days
- Product code: MVL (Cord, Retraction)
- Device class: U
- 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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K243910: Retraxil (2025), 0 descendants of its own

## Indications for use
LiquiCord is intended for temporary retraction and hemostasis of the gingival margin during dental procedures such as dental impressions and the seating of temporary and permanent restorations

Source page: https://510kreport.com/device/K092384
Methodology: https://510kreport.com/methodology