# K962065: 3M Vitrebond Light Cure Glass Ionomer/Base

- Pathway: 510(k) (Traditional)
- Applicant: 3M Company
- Decided: Jul 18, 1996 after 51 days
- Product code: EMA (Cement, Dental)
- Device class: 2
- Regulation: 21 CFR 872.3275
- 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 K882821 (1988). 2 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K882821: Vitrabond Light Cure Glass Ionomer Liner, 3M Company (1988) Summary page 1.
- K915668: Bisco Cavity Cleanser, Bisco, Inc. (1992) Summary page 1.
- (no number) Uni-Etch™ (part of One-Step Universal Dentin Adhesive): named in the summary without a submission number

## Most influential descendants
- K991172: Ionosit Bond (1999), 0 descendants of its own

## Indications for use
3M™ Vitrebond™ Light Cure Glass Ionomer Liner/Base is indicated for lining and basing applications under composite, amalgam, ceramic, and metal restorations.

Source page: https://510kreport.com/device/K962065
Methodology: https://510kreport.com/methodology