VISIBLY

FDA Device Registration & Listing · Wilmington, DE, US · Registration 3020029799

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
3020029799
FEI Number
3020029799
Entity Name
VISIBLY
City/State/Country
Wilmington, DE, US
Establishment Address
251 Little Falls Drive, County of New Castle, Wilmington, DE 19808, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Visibly (Owner Number: 10048154)
Owner / Operator Contact Address
16217 Borelle Circle, Naples, FL 34110, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Single Device Acuity Product (SDAP) Visibly Acuity Product (VAP) Fast Acuity (FA)

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
QTO Digital Visual Acuity Test Ophthalmic Class 1 886.1150 2023-11-08

Official Correspondent

Paul Foley

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Visibly
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 3020029799. Last updated year: 2026. Please use registration number 3020029799 when referencing this establishment in official correspondence.
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