Suzuken Co., Ltd.
Country not established
- Devices
- 25
What Suzuken Co., Ltd. makes
Suzuken Co., Ltd. manufactures single-channel and multi-channel digital electrocardiographs (ECGs), including models like the KENZ ECG 108, KENZ ECG 110, and KENZ-CARDICO 1201. Their portfolio also includes ECG interpretation devices, disposable electrodes (e.g., EASYRODE), gel pads (KENZ-GELECT GEL PAD), and accessories such as the KENZ-45M. These devices are designed for cardiac monitoring and diagnostic purposes in clinical settings.
The company’s ECG devices fall under Class II regulatory classification in the US, requiring 510(k) clearance through the FDA. Their products are listed in the FDA’s 510(k) registry, and the company operates from the United States.
Catalogue
Search and filter all 25 devicesCompany details
- DUNS number
- 690583984
- [email protected]
- Phone
- +1(800)558-7044
Frequently asked questions
How many devices does SUZUKEN CO., LTD. have in the registry?
The registry currently lists 25 devices for SUZUKEN CO., LTD.. Devices recorded under merged duplicate company entries are counted once.
Which registries list SUZUKEN CO., LTD.'s devices?
Among its 25 most recently registered devices, SUZUKEN CO., LTD. has devices listed in FDA 510(k) (13 devices) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do SUZUKEN CO., LTD.'s devices fall under?
Among its 25 most recently registered devices, the classes recorded for SUZUKEN CO., LTD.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from SUZUKEN CO., LTD. in the registry?
The most recently registered devices listed for SUZUKEN CO., LTD. include SEER Light Connect, SEER Light Extend, SEER Light and SEER Light Patient Cable 2CH AHA CF.