Cadwell Industries, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Cadwell Industries, Inc. has 12 FDA 510(k) cleared neurology devices. Based in Kennewick, US.
Latest FDA clearance: Dec 2025. 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.
FDA 510(k) cleared devices by Cadwell Industries, Inc.
12 devices
Cleared
Dec 14, 2025
Hypnos (369054-200)
Neurology
268d
Cleared
Dec 18, 2024
Bluebird Single-Use Respiratory Effort Belt
Anesthesiology
125d
Cleared
Aug 17, 2023
Cadwell Guardian
Neurology
182d
Cleared
Sep 29, 2020
Cadwell Apollo System
Neurology
90d
Cleared
Feb 20, 2020
ApneaTrak
Neurology
150d
Cleared
Nov 23, 2019
Cadwell Bolt Software
Neurology
243d
Cleared
Sep 01, 2018
Cadwell Zenith System
Neurology
89d
Cleared
Jul 17, 2018
Cadwell Apollo System
Neurology
167d
Cleared
Mar 02, 2017
Cascade IOMAX Intraoperative Monitor
Neurology
209d
Cleared
Mar 01, 2017
Cadwell Sierra Summit, Cadwell Sierra Ascent
Neurology
188d
Cleared
Nov 08, 2016
Cadwell AmpliScan
Neurology
210d
Cleared
Jan 29, 2014
CADWELL FLEX EEG/PSG
Neurology
90d