# K102844: All-Bound 3

- Pathway: 510(k) (Special)
- Applicant: Bisco, Inc.
- Decided: Oct 29, 2010 after 30 days
- Product code: KLE (Agent, Tooth Bonding, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3200
- 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 K910860 (1991). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K910860: All-Bond 2, Bisco, Inc. (1991) Summary page 1.

## Indications for use
The principle uses of All Bond 3 are: *All Direct Restorations *All Indirect Restorations *Intra-oral Repair *Desensitizing/sealing of tooth stmucture

Source page: https://510kreport.com/device/K102844
Methodology: https://510kreport.com/methodology