Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3013259337

FEI Number

3013259337

Entity Name

Tykables LLC

City/State/Country

Elk Grove Village, IL, US

Establishment Address

1001 Arthur Ave, Elk Grove Village, IL 60007, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Tykables LLC (Owner Number: 10058115)

Owner / Operator Contact Address

1001 Arthur Ave, Elk Grove Village, IL 60007, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Tykables

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2025-08-18

Official Correspondent

James Ward

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Tykables LLC

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 3013259337. Last updated year: 2026. Please use registration number 3013259337 when referencing this establishment in official correspondence.