# K241445: K-Bond Universal

- Pathway: 510(k) (Traditional)
- Applicant: Spident Co., Ltd.
- Decided: Jul 22, 2024 after 61 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: 7 generations back to K900510 (1990). 36 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 38 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K110302: Adhesive Exl-759, 3M Espe AG (2011) Summary page 5.

## Most influential descendants
- K252151: els unibond (2025), 0 descendants of its own

## Indications for use
-Bonding of all direct composite restorations -Bonding of dual/self cure composite and core build-ups -Repairs of composite fillings -Root surface desensitization

Source page: https://510kreport.com/device/K241445
Methodology: https://510kreport.com/methodology