Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2432426

FEI Number

2432426

Entity Name

TWOROGER ASSOCIATES, LTD.

City/State/Country

NEW YORK, NY, US

Establishment Address

594 BROADWAY, SUITE 801, NEW YORK, NY 10012, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Tworoger Associates, LTD. DBA Modo Eyewear (Owner Number: 9024852)

Owner / Operator Contact Address

594 BROADWAY, SUITE 801, --, New York, NY 10012, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Modo Eyewear Modo Eyewear Readers, Magnifying

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRX	Case, Contact Lens	Ophthalmic	Class 2	886.5928	2025-08-15
HOI	Spectacle, Magnifying	Ophthalmic	Class 1	886.5840	2023-01-11

Official Correspondent

Anelle Narcisse

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tworoger Associates, LTD. DBA Modo Eyewear

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 2432426. Last updated year: 2026. Please use registration number 2432426 when referencing this establishment in official correspondence.