Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3012102743

FEI Number

3012102743

Entity Name

VISTA LIFESCIENCES, INC.

City/State/Country

Englewood, CO, US

Establishment Address

7375 S Peoria St Ste 210, Englewood, CO 80112, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Vista LifeSciences, Inc. (Owner Number: 10050147)

Owner / Operator Contact Address

7375 S Peoria St. Suite 210, Englewood, CO 80112, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

ANAM Test System ANAM Test System: Military Battery ANAM Test System

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
POM	Computerized Cognitive Assessment Aid For Concussion	Neurology	Class 2	882.1471	2021-12-23
PTY	Computerized Cognitive Assessment Aid, Exempt	Neurology	Class 2	882.1470	2017-11-21

Official Correspondent

Lori White

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vista LifeSciences, Inc.

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 3012102743. Last updated year: 2026. Please use registration number 3012102743 when referencing this establishment in official correspondence.