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Data / Medical devices / United States / Zeto, Inc.

Zeto, Inc.: FDA-registered device maker in Raleigh, NC, United States, 3 510(k) clearances

Zeto, Inc. is registered with the FDA (registration 3021826057) in Raleigh, NC, United States. It lists 2 device types. The FDA files 3 510(k) clearances under its listings, the newest dated March 13, 2026. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
3021826057
Address
5565 Centerview Dr Ste 105, Raleigh, NC, United States, 27606
Owner or operator
Zeto, Inc. (10057738)
Roles
Repackager or relabeler
First device listed
May 20, 2018
Registered through
2026
Brand names listed
New Wave, WR19, Zeto ONE

Devices it lists

DeviceProduct codeClassRoleSource
Electrode, CutaneousGXY2Repackager or relabeleraccessdata.fda.gov
Full-Montage Standard ElectroencephalographGWQ2Repackager or relabeleraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
March 13, 2026K260455New Wave SystemGWQSubstantially EquivalentZeto, Inc.accessdata.fda.gov
April 30, 2024K233403Flexset SystemGWQSubstantially EquivalentZeto, Inc.accessdata.fda.gov
April 17, 2018K172735WR19 SystemGWQSubstantially EquivalentZeto, Inc.accessdata.fda.gov

Compare with other makers

Updated March 13, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.