# K972573: Liqcrylic Pro Dental Resin

- Pathway: 510(k) (Traditional)
- Applicant: Dentsply Intl.
- Decided: Sep 16, 1997 after 68 days
- Product code: EBI (Resin, Denture, Relining, Repairing, Rebasing)
- Device class: 2
- Regulation: 21 CFR 872.3760
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K902115 (1990). 1 ancestor in all.
62 later devices descend from it; 2 cite it directly.
0 of 64 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K902115: Palapress (R) Vario Resin, Kulzer, Inc. (1990) Summary page 1.

## Most influential descendants
- K990763: Vitron M (1999), 60 descendants of its own
- K991220: Vitron H (1999), 60 descendants of its own
- K992645: Sinfony (1999), 59 descendants of its own
- K071131: UNO (2007), 35 descendants of its own
- K110302: Adhesive Exl-759 (2011), 34 descendants of its own

## Indications for use
Used in the fabrication, repair or rebasing of complete or partial removable dentures and other removable dental appliances.

Source page: https://510kreport.com/device/K972573
Methodology: https://510kreport.com/methodology