Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008994998

FEI Number

3008994998

Entity Name

EYETECH DIGITAL SYSTEMS

City/State/Country

Tempe, AZ, US

Establishment Address

2141 E Broadway Rd, Suite 202, Tempe, AZ 85282, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

EyeTech Digital Systems (Owner Number: 10060724)

Owner / Operator Contact Address

1128 E Greenway Street, Suite 1, Mesa, AZ 85203, 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
ILQ	System, Communication, Powered	Physical Medicine	Class 2	890.3710	2019-06-17

Official Correspondent

Robert Chappell

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

EyeTech Digital Systems

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0004-2016	Lifeline Systems, Incorporated	2	Philips GoSafe Mobile Help Button; 7000MHB. Personal Emergency Response System.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008994998. Last updated year: 2026. Please use registration number 3008994998 when referencing this establishment in official correspondence.