Jeol
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Jeol is a medical device manufacturer, with 17 devices listed in FDA GUDID and FDA 510(k) (FDA Class I, II and III) as of 13 Nov 2026.
- Devices
- 17
Registry facts
- Registries
- FDA GUDID 16
- FDA 510(k) 1
- Device classes
- FDA Class I 10
- FDA Class II 6
- FDA Class III 1
What Jeol makes
Jeol manufactures in vitro diagnostic (IVD) reagents and accessories for clinical chemistry, including enzyme-based assays, ion-selective electrodes (ISE), and reference solutions. Their portfolio covers electrolyte measurement devices such as sodium, potassium, and chloride electrodes, as well as maintenance solutions like cuvette washes, probe washes, and detergent solutions. Standardized reference materials, including ISE serum and urine standards, are also part of their product line.
Jeol’s devices are regulated under FDA classifications, including Class I, Class II, and Class III, with submissions recorded in the 510(k) and UDI registries. The company’s products are listed in the United States.
Catalogue
Search and filter all 17 devicesFrequently asked questions
How many devices does Jeol have in the registry?
The registry currently lists 17 devices for Jeol. Devices recorded under merged duplicate company entries are counted once.
Which registries list Jeol's devices?
Among its 17 most recently registered devices, Jeol has devices listed in FDA 510(k) (1 device) and FDA GUDID (16 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Jeol's devices fall under?
Among its 17 most recently registered devices, the classes recorded for Jeol's devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.
What are the newest devices from Jeol in the registry?
The most recently registered devices listed for Jeol include Reagent Probe Wash S 781611482, Cuvette Wash Solution 7 781611423, ISE Buffer (IS) 781611334 and Reagent Probe Wash 2 781611466.