Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3007883990

FEI Number

3007883990

Entity Name

SMARTBOX US

City/State/Country

Cedar Falls, IA, US

Establishment Address

1100 Technology PKY, Cedar Falls, IA 50613, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Talk To Me Technologies DBA Smartbox US (Owner Number: 10031517)

Owner / Operator Contact Address

1100 Technology PRKY, Cedar Falls, IA 50613, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

L10 L10 Slimline Talk Pad 10 G10X Slimline G13 Talk Pad 8 L8 G15 L8 Slimline Wego 10A-D Wego 7A-D Wego 13A-D WegoWrite-D Wego 5A-D Zuvo 10-D Zuvo 16-D Zuvo 12-D Talk Pad Wego 8 Talk Pad Wego 10 Grid Pad 16 Grid Pad Go 10 Grid Pad 13 G16 G10X G10

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	2010-02-08

Official Correspondent

Amanda Buhrow

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Talk To Me Technologies DBA Smartbox US

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.

Similar Registrations

Registration Number	Establishment Name	Location
3010824482	RELIANCE MOBILITY LLC	Columbia, TN, US
3008994998	EYETECH DIGITAL SYSTEMS	Tempe, AZ, US
3005301283	DYNAVOX Group AB	Stockholm, SE
3007275470	JABBLA	Gent Oost-Vlaanderen, BE
3018783526	CEVA LOGISTICS NETHERLANDS BV (Venray)	Oostrum Limburgh, NL

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007883990. Last updated year: 2026. Please use registration number 3007883990 when referencing this establishment in official correspondence.