# K261695: Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)

- Pathway: 510(k) (Traditional)
- Applicant: Guilin Kevin Peter Technology Co., Ltd.
- Decided: Aug 31, 2026 after 101 days
- Product code: EBF (Material, Tooth Shade, Resin)
- Device class: 2
- Regulation: 21 CFR 872.3690
- 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 K042819 (2004). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K221695: 3M Filtek Supreme Flowable Restorative, 3M Company Espe Dental Products (2022) Summary page 6.

## Indications for use
Intended purpose: This product can be used for direct restoration of anterior and posterior. Indications: * Direct Restoration of all cavity classes (I-V) * Base/liner under direct restorations * Repair of small defects in esthetic indirect restorations * Repair of resin and acrylic temporary materials * Pit and fissure sealant

Source page: https://510kreport.com/device/K261695
Methodology: https://510kreport.com/methodology