VEO OPHTHALMICS LLC

FDA Device Registration & Listing · West Chester, OH, US · Registration 3014399865

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
3014399865
FEI Number
3014399865
Entity Name
VEO OPHTHALMICS LLC
City/State/Country
West Chester, OH, US
Establishment Address
10184 International Boulevard, West Chester, OH 45246, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198
Owner / Operator
VEO Ophthalmics LLC (Owner Number: 10058391)
Owner / Operator Contact Address
10184 International Boulevard, Cincinnati, OH 45246, US
Initial Importer Flag
Y
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
P170039

All Registered Proprietary Names

CUSTOMFLEX ARTIFICIAL IRIS

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QBT Artificial Iris Unknown Class 3 N/A 2022-12-27

Official Correspondent

Ron Gilliland

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

VEO Ophthalmics LLC
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 3014399865. Last updated year: 2026. Please use registration number 3014399865 when referencing this establishment in official correspondence.
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