# Pentaferte Italia S.R.L.

- Location (FDA's records): Campli, IT
- FDA decisions: 3 (2017–2022): 3 510(k) clearances
- Product codes: PNR (2), NGT (1)
- Predicates its devices cite: 4 (1 its own); citations of its devices by later devices: 2 (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
- Neomed, Inc.: 2 (https://510kreport.com/company/neomed)
- Medxl, Inc.: 1 (https://510kreport.com/company/medxl)

## Firms that cite its devices most
- Jiangsu Caina Medical Co.,Ltd: 1 (https://510kreport.com/company/jiangsu-caina-medical)

## Its most-cited devices
- K161141: ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT (2017), cited by 2

## Recent decisions
- K214080: Pentaflush (Jul 20, 2022)
- K211661: ENFit enteral syringes (NUTRIFIT) (Feb 28, 2022)
- K161141: ENFit Enteral Pump Syringes PENTA ENFit, ENFit Enteral Pump Syringes NUTRIFIT (Mar 22, 2017)

Source page: https://510kreport.com/company/pentaferte-italia