Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014692331

FEI Number

3014692331

Entity Name

EPITEL

City/State/Country

Salt Lake City, UT, US

Establishment Address

465 South 400 East, Suite 250, Salt Lake City, UT 84111, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Epitel (Owner Number: 10082545)

Owner / Operator Contact Address

465 S 400 E, Suite 250, Salt Lake City, UT 84111, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K231779

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OMB	Automatic Event Detection Software For Full-Montage Electroencephalograph	Neurology	Class 2	882.1400	2024-01-11

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Epitel

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014692331. Last updated year: 2026. Please use registration number 3014692331 when referencing this establishment in official correspondence.