# Drfp, Ltd.

- Location (FDA's records): Amsterdam, GB
- FDA decisions: 2 (2010–2012): 2 510(k) clearances
- Product codes: KIF (2)
- Predicates its devices cite: 2 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Meta Biomed Co., Ltd.: 1 (https://510kreport.com/company/meta-biomed)

## Firms that cite its devices most
- Essential Dental Systems, Inc.: 2 (https://510kreport.com/company/essential-dental-systems)

## Its most-cited devices
- K100248: DRFP Prosmart Root Canal Obturation System, Propoints 4% 6%, PT, S (2010), cited by 2
- K120048: DRFP Propoints, Propoints 4%, Propoints 6%, Propoints PT, Propoints S (2012), cited by 1

## Recent decisions
- K120048: DRFP Propoints, Propoints 4%, Propoints 6%, Propoints PT, Propoints S (Jun 20, 2012)
- K100248: DRFP Prosmart Root Canal Obturation System, Propoints 4% 6%, PT, S (Oct 22, 2010)

Source page: https://510kreport.com/company/drfp