# K120048: DRFP Propoints, Propoints 4%, Propoints 6%, Propoints PT, Propoints S

- Pathway: 510(k) (Traditional)
- Applicant: Drfp, Ltd.
- Decided: Jun 20, 2012 after 166 days
- Product code: KIF (Resin, Root Canal Filling)
- Device class: 2
- Regulation: 21 CFR 872.3820
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K960548 (1996). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K100248: DRFP Prosmart Root Canal Obturation System, Propoints 4% 6%, PT, S, Drfp, Ltd. (2010) Summary page 1.

## Most influential descendants
- K202281: EDS Bioceramic Sealer (Bioseal) (2021), 0 descendants of its own

## Indications for use
DRFP propoint obturation points are designed for permanent sealing of root canals when used with DRFP smartpaste Dental Sealer or Brasseler USA EndoSequence® BC Sealer following established endodontic procedures by qualified healthcare professionals.

Source page: https://510kreport.com/device/K120048
Methodology: https://510kreport.com/methodology