Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3029658405

FEI Number

3029658405

Entity Name

Vistim Labs Inc.

City/State/Country

Claymont, DE, US

Establishment Address

2093 Philadelphia Pike #3690, Claymont, DE 19703, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Vistim Labs (Owner Number: 10088726)

Owner / Operator Contact Address

2093 Philadelphia Pike, 3690, Claymont, DE 19703, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

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
PTY	Computerized Cognitive Assessment Aid, Exempt	Neurology	Class 2	882.1470	2023-10-05

Official Correspondent

James Hamet

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vistim Labs

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 3029658405. Last updated year: 2026. Please use registration number 3029658405 when referencing this establishment in official correspondence.