Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3015867300

FEI Number

3015867300

Entity Name

OLLEYES, INC.

City/State/Country

Summit, NJ, US

Establishment Address

350 Springfield Ave. Suite 200, Summit, NJ 07901, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Olleyes, Inc. (Owner Number: 10061261)

Owner / Operator Contact Address

350 Springfield Ave. Suite 200, Summit, NJ 07901, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VisuALL VisuALL

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
HLG	Pupillometer, Ac-Powered	Ophthalmic	Class 1	886.1700	2022-05-09
HPT	Perimeter, Automatic, Ac-Powered	Ophthalmic	Class 1	886.1605	2019-10-03

Official Correspondent

Alberto Gonzalez Garcia

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Olleyes, 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 3015867300. Last updated year: 2026. Please use registration number 3015867300 when referencing this establishment in official correspondence.