Medical Device Manufacturer · US , Kennewick , WA

Cadwell Industries, Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2014

Recent clearances: Hypnos (369054-200), Bluebird Single-Use Respiratory Effort Belt, Cadwell Guardian

Total

Cleared

Denied

Cadwell Industries, Inc. has 13 FDA 510(k) cleared neurology devices. Based in Kennewick, US.

Latest FDA clearance: Jun 2026. Active since 2014.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Cadwell Industries, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Cadwell Industries, Inc.

13 devices

1-12 of 13

Cleared Jun 26, 2026

Charlotte ACC25 Surface Electrode Array

Bluebird Single-Use Respiratory Effort Belt

K242424 · MNR

Anesthesiology · 125d

Cadwell Apollo System

Cadwell Bolt Software

K190760 · OLT

Neurology · 243d

Cleared Sep 01, 2018

Cadwell Zenith System

K181466 · GWQ

Neurology · 89d

Cleared Jul 17, 2018

Cadwell Apollo System

K180269 · GWQ

Neurology · 167d

Cleared Mar 02, 2017

Cascade IOMAX Intraoperative Monitor

K162199 · GWF

Neurology · 209d

Cleared Mar 01, 2017

Cadwell Sierra Summit, Cadwell Sierra Ascent

Cadwell Industries, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Cadwell Industries, Inc.

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