ZYTO Technologies, Inc.

FDA Device Registration & Listing · Lehi, UT, US · Registration 3008493238

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008493238
FEI Number
3008493238
Entity Name
ZYTO Technologies, Inc.
City/State/Country
Lehi, UT, US
Establishment Address
1401 N. Thanksgiving Way, STE 325, Lehi, UT 84048, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device
Owner / Operator
ZYTO Technologies, Inc. (Owner Number: 10043910)
Owner / Operator Contact Address
1401 N. Thanksgiving Way, STE 325, Lehi, UT 84048, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

ZYTO Hand Cradle ZYTO Software

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
GZO Device, Galvanic Skin Response Measurement Neurology Class 2 882.1540 2013-04-04
OUG Medical Device Data System General Hospital Class 1 880.6310 2014-07-28

Official Correspondent

Vaughn Cook

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

ZYTO Technologies, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008493238. Last updated year: 2026. Please use registration number 3008493238 when referencing this establishment in official correspondence.
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