Natus Manufacturing Limited is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Natus Manufacturing Limited - FDA 510(k) Cleared Devices
Recent clearances: Grass® MR Conditional/CT Cup Electrodes, Allergan Botox Needle Electrode
4
Total
4
Cleared
0
Denied
Natus Manufacturing Limited has 4 FDA 510(k) cleared medical devices. Based in Gort, IE.
Latest FDA clearance: Aug 2024. Active since 2015. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Natus Manufacturing Limited Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Natus Manufacturing Limited
4 devices
Cleared
Aug 29, 2024
Grass® MR Conditional/CT Cup Electrodes
Neurology
22d
Cleared
Jun 29, 2018
Allergan Botox Needle Electrode
Neurology
196d
Cleared
Mar 02, 2017
Myoject Luer Lock Needle Electrode
Neurology
283d
Cleared
Aug 28, 2015
Dantec DCN Disposable Concentric Needle Electrodes-25mm, Dantec DCN...
Neurology
270d