Vivid Vision

FDA Device Registration & Listing · San Francisco, CA, US · Registration 3014400613

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
3014400613
FEI Number
3014400613
Entity Name
Vivid Vision
City/State/Country
San Francisco, CA, US
Establishment Address
2565 3RD ST STE 318, San Francisco, CA 94107, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
Vivid Vision Inc (Owner Number: 10057298)
Owner / Operator Contact Address
2565 3rd Street Suite 318, San Francisco, CA 94107, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Vivid Vision Vivid Vision

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HPT Perimeter, Automatic, Ac-Powered Ophthalmic Class 1 886.1605 2023-05-03
NXR Fixation, Vision Training, Binocular Ophthalmic Class 1 886.1290 2021-12-01

Official Correspondent

James Blaha

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vivid Vision 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 3014400613. Last updated year: 2026. Please use registration number 3014400613 when referencing this establishment in official correspondence.
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