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Cadwell Industries, Inc.

United States·US-MF-000001265

Last updated September 17, 2026

About

Helping you help others. Cadwell helps patients, physicians, clinics, and hospitals around the world by delivering innovative neurodiagnostic and neuromonitoring solutions, improving clinical efficiency, and providing market leading customer support.

From the manufacturer's own website. Source

Information

Country
United States
Address
909, North Kellogg St, Kennewick, United States
Phone
+1 800 245 3001
PRRC Contact
Beata (Becky) Corral
EUDAMED SRN
US-MF-000001265
FDA FEI Number
3020018
DUNS Number
—

Catalogue (335)

Page 1 of 7
DeviceModel / ReferenceRegistriesClassStatus
Cadwell 302523-200-0100
FDA UDI
Class IIActive
Sierra Ascent 190277-200
FDA UDI
Class IIActive
Cadwell Replacement Stimulator Probe 339080-200
FDA UDI
Class IIActive
Cascade IOMAX Intraoperative Monitor 190309-200
FDA UDI
Class IIActive
Cadwell Mini-Crocodile Clip Lead Wire 302160-200
FDA UDI
Class IIActive
Cadwell Disposable Bent Ball-Tip Probe 302405-000
FDA UDI
Class IIUnknown
Cadwell Patch Electrode with Snap Connector 302313-200
FDA UDI
Class IIActive
Cadwell 302548-200-0080
FDA UDI
Class IIActive
Zenith 190307-200
FDA UDI
Class IIActive
Cascade 190201-200
FDA UDI
Class IIActive
ApneaTrak 190306-200
FDA UDI
Class IIActive
Cadwell Disposable Subdermal Needle Electrode 302353-000-060
FDA UDI
Class IIUnknown
Cadwell Bar Electrodes 302287-000
FDA UDI
Class IIActive
EasyNet 190211-200
FDA UDI
Class IIActive
Cascade 190258-200
FDA UDI
Class IIActive
Cadwell Gold Cup Electrode 203104-200
FDA UDI
Class IIActive
Cadwell Disposable Tab Electrodes 302217-000
FDA UDI
Class IIActive
Cadwell Disposable Surface Electrode 302854-000-100
FDA UDI
Class IIUnknown
Cascade IOMAX Intraoperative Monitor 199305-200
FDA UDI
Class IIActive
Cadwell Replacement Remote Input Extender Pod 302152-200
FDA UDI
Class IIActive
Cadwell Disposable Ground Electrodes 302288-000
FDA UDI
Class IIActive
Cadwell 302295-000-020
FDA UDI
Class IIActive
Cadwell Disposable Subdermal Needle Electrode 302353-000-040
FDA UDI
Class IIUnknown
Sierra Wave 199220-200
FDA UDI
Class IIActive
IOMAX Extender Pod 362068-000
FDA UDI
Class IIActive
Sierra Summit 190274-200
FDA UDI
Class IIActive
Cadwell Lead Wire 198261-200
FDA UDI
Class IIUnknown
Easy III 190230-200
FDA UDI
Class IIActive
Cadwell 302553-200-0000
FDA UDI
Class IIActive
Cadwell Single Disc Electrode 302139-200
FDA UDI
Class IIActive
Cadwell Disposable Bent Ball-Tip Probe 302428-000
FDA UDI
Class IIUnknown
Cadwell 302548-200-0280
FDA UDI
Class IIActive
Cadwell 302516-200-0480
FDA UDI
N/AActive
Cadwell Disposable Tab Electrodes 302285-000
FDA UDI
Class IIActive
Cascade IOMAX Intraoperative Monitor 190295-200
FDA UDI
Class IIActive
Cadwell Interconnect Cable 302785-200
FDA UDI
Class IIActive
Cadwell 302529-200-0080
FDA UDI
Class IIActive
Cadwell Disposable Subdermal Needle Electrode 302353-000-100
FDA UDI
Class IIUnknown
Cadwell Disposable Ring Electrodes 302286-000
FDA UDI
Class IIActive
Cadwell Disposable Monopolar Probe 302427-000-200
FDA UDI
Class IIUnknown
Cadwell Patented Multi-Stage Clip 302775-200
FDA UDI
Class IIActive
Cadwell Twisted Disposable Subdermal Needle Electrode 302820-000-060
FDA UDI
Class IIUnknown
Cadwell Stim Probe 362052-200
FDA UDI
Class IIActive
Cadwell 302295-000-032
FDA UDI
Class IIActive
Cadwell Lead Wire 302774-200
FDA UDI
Class IIActive
Cadwell Disposable Hook Probes 302423-000
FDA UDI
Class IIUnknown
Cadwell 302522-200-1053
FDA UDI
Class IIUnknown
Cadwell Disposable Patient Starter Kit 302221-200
FDA UDI
Class IIUnknown
Cadwell Ring Electrode 302243-200
FDA UDI
Class IIActive
Cadwell Extension Lead Wire 302130-200
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
May 17, 2024Z-2349-2024—open, classified

Electroneurodiagnostic medical device may contain a defective printed circuit board which may cause damage to the other internal components resulting in unintended electrical stimulation.

Apr 23, 2024Z-1882-2024—open, classified

There is the potential that an electroneurodiagnostic medical device insulator may be installed incorrectly which could result in arcing to patient connections resulting in potential unintended shock to the patient.