# K974772: Ufi Gel C

- Pathway: 510(k) (Traditional)
- Applicant: Voco GmbH
- Decided: Feb 10, 1998 after 50 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
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
- K111178: Juell Soft Cure (2011), 0 descendants of its own

## Indications for use
Ufi Gel C is intended for use as a permanently soft relining for total and partial dentures. - to relieve pressure from pressure spots - to dam the palatal vibrating line in cases of flabby ridge and insufficient adhesion - to cushion sharp-edged alveolar processes - to support the healing process in implantology

Source page: https://510kreport.com/device/K974772
Methodology: https://510kreport.com/methodology