# K990763: Vitron M

- Pathway: 510(k) (Traditional)
- Applicant: Espe Dental AG
- Decided: May 25, 1999 after 78 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: 2 generations back to K902115 (1990). 2 ancestors in all.
60 later devices descend from it; 1 cites it directly.
0 of 63 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.
- K972573: Liqcrylic Pro Dental Resin, Dentsply Intl. (1997) Summary page 1.

## Most influential descendants
- 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
- K042929: Estenia C&B (2004), 12 descendants of its own
- K112118: Dreambond (2011), 8 descendants of its own

## Indications for use
Denture base material for: Completion of metal frameworks Partial and total denture rebasing Extension of partial dentures Repairs Fabrication of partial and total dentures

Source page: https://510kreport.com/device/K990763
Methodology: https://510kreport.com/methodology