# Mediplus, Ltd.

- Location (FDA's records): High Wycombe, Bucks, GB
- FDA decisions: 4 (2002–2014): 4 510(k) clearances
- Product codes: KLA (2), KOB (1), CCK (1)
- Predicates its devices cite: 5 (0 its own); citations of its devices by later devices: 4 (0 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
- Fortune Medical Instrument Corp.: 2 (https://510kreport.com/company/fortune-medical-instrument)
- Rusch, Inc.: 1 (https://510kreport.com/company/rusch)
- Cook Urological, Inc.: 1 (https://510kreport.com/company/cook-urological)
- Medsys, S.A.: 1 (https://510kreport.com/company/medsys)

## Firms that cite its devices most
- Sarmed Srl: 2 (https://510kreport.com/company/sarmed)
- Cook, Inc.: 1 (https://510kreport.com/company/cook)
- Medtronic Vascular: 1 (https://510kreport.com/company/medtronic-vascular)

## Its most-cited devices
- K013704: Mediplus Single Use GI Manometry Catheter (2002), cited by 2
- K132890: Suprapubic Catheter and Introducer Set (2014), cited by 1
- K031617: Mediplus Single Use Lower GI Manometry Catheter (2004), cited by 1

## Recent decisions
- K132890: Suprapubic Catheter and Introducer Set (Jan 17, 2014)
- K131339: Capnomask (Nov 25, 2013)
- K031617: Mediplus Single Use Lower GI Manometry Catheter (Jan 16, 2004)
- K013704: Mediplus Single Use GI Manometry Catheter (Aug 5, 2002)

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