Honeywell, Inc.
United StatesFDA applicant, unverified
- Devices
- 69
What Honeywell, Inc. makes
Honeywell, Inc. manufactures portable and bedside cardiac monitoring devices, including defibrillators (e.g., ED 425, 74DRK), patient monitors (e.g., CM111, CM112), and ECG monitors (e.g., RM102). The company also produces diagnostic imaging tools like the ULTRA IMAGER and motility assessment equipment such as the esophageal motility apparatus. Additional offerings include electrophysiological recording systems (e.g., AR110, N3B-EEG amplifier), pulse/phonocardiography channels, and medical data management solutions for reporting and database tracking.
The company’s devices are classified under FDA categories Class I, Class II, and Class III, with submissions recorded in the FDA’s 510(k) registry. These products are listed under U.S. regulatory oversight, reflecting compliance with U.S. medical device requirements. The manufacturer operates from the United States.
Catalogue
Search and filter all 69 devicesShowing 1-50 of 69
Frequently asked questions
How many devices does Honeywell, Inc. have in the registry?
The registry currently lists 69 devices for Honeywell, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Honeywell, Inc.'s devices?
Among its 50 most recently registered devices, Honeywell, Inc. has devices listed in FDA 510(k) (50 devices).
What risk classes do Honeywell, Inc.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Honeywell, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Honeywell, Inc. in the registry?
The most recently registered devices listed for Honeywell, Inc. include PORTABLE DEFIBRILLATOR/MONITOR ED 425, ULTRA IMAGER, PATIENT MONITOR CM111, 112 and ESOPHAGEAL MOTILITY APPARATUS.