Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3027718329

FEI Number

3027718329

Entity Name

EYECHEQ, INC

City/State/Country

Miami, FL, US

Establishment Address

3250 NE 1st Ave Ste 305, Miami, FL 33137, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

EyeCheq, INC (Owner Number: 10088501)

Owner / Operator Contact Address

3250 NE 1st Ave Ste 305, Miami, FL 33137, 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
HMF	Stand, Instrument, Ac-Powered, Ophthalmic	Ophthalmic	Class 1	886.1860	2023-08-02
QTO	Digital Visual Acuity Test	Ophthalmic	Class 1	886.1150	2023-08-02

Official Correspondent

Ali Khoshnevis

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EyeCheq, 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 3027718329. Last updated year: 2026. Please use registration number 3027718329 when referencing this establishment in official correspondence.