Zeto Inc
United StatesFDA applicant, unverified
Zeto Inc is a medical device manufacturer, with 39 devices listed in FDA GUDID and FDA 510(k) (FDA Class II) as of 13 Nov 2026.
- Devices
- 39
Registry facts
- Registries
- FDA GUDID 36
- FDA 510(k) 3
- Device classes
- FDA Class II 39
- Identifiers
- DUNS 079582566
What Zeto Inc makes
Zeto Inc manufactures electroencephalograph (EEG) systems, including display units, head units, and electrode sets for both short- and long-term monitoring. Their portfolio includes single-use scalp electrodes, cable extensions, and medical-grade PCs designed for clinical EEG applications. Additional products like the Soft Flex-T and basic electrode sets cater to specific EEG recording needs.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s 510(k) and UDI registries. Zeto Inc operates from the United States.
Catalogue
Search and filter all 39 devicesCompany details
- DUNS number
- 079582566
- support@zetoinc.com
- Phone
- 8339386334
Frequently asked questions
How many devices does ZETO INC have in the registry?
The registry currently lists 39 devices for ZETO INC. Devices recorded under merged duplicate company entries are counted once.
Which registries list ZETO INC's devices?
Among its 39 most recently registered devices, ZETO INC has devices listed in FDA 510(k) (3 devices) and FDA GUDID (36 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do ZETO INC's devices fall under?
Among its 39 most recently registered devices, the classes recorded for ZETO INC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from ZETO INC in the registry?
The most recently registered devices listed for ZETO INC include Zeto TTL Extension Unit ZP-141-11011, Zeto Extension Unit ZP-141-11001, New Wave Head Unit - Small ZP-120-11051 and New Wave Display Unit ZP-140-11021.