# Natus Manufacturing Limited

- Location (FDA's records): Gort, IE
- FDA decisions: 4 (2015–2024): 4 510(k) clearances
- Product codes: IKT (3), GXY (1)
- Predicates its devices cite: 4 (0 its own); citations of its devices by later devices: 2 (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
- Medelec, Inc. D.B.A. Teca Corp.: 2 (https://510kreport.com/company/medelec-dba-teca)
- Rhythmlink International, LLC: 1 (https://510kreport.com/company/rhythmlink-international)
- Carefusion 209, Inc.: 1 (https://510kreport.com/company/carefusion-209)

## Firms that cite its devices most
- Technomed Europe: 1 (https://510kreport.com/company/technomed-europe)
- Ambu A/S: 1 (https://510kreport.com/company/ambu-a-s)

## Its most-cited devices
- K242346: Grass® MR Conditional/CT Cup Electrodes (2024), cited by 2

## Recent decisions
- K242346: Grass® MR Conditional/CT Cup Electrodes (Aug 29, 2024)
- K173815: Allergan Botox Needle Electrode (Jun 29, 2018)
- K161430: Myoject Luer Lock Needle Electrode (Mar 2, 2017)
- K143433: Dantec DCN Disposable Concentric Needle Electrodes-25mm, Dantec DCN Disposable Concentric Needle Electrodes-37mm, Dantec DCN Disposable Concentric Needle Electrodes-50mm, Dantec DCN Disposable Concentric Needle Electrodes-75mm (Aug 28, 2015)

Source page: https://510kreport.com/company/natus-manufacturing