Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008243322

FEI Number

3008243322

Entity Name

S-COMM, INC.

City/State/Country

Raytown, MO, US

Establishment Address

6238 HADLEY ST, Raytown, MO 64133, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

sComm Inc. (Owner Number: 10050271)

Owner / Operator Contact Address

6238 Hadley Street, Raytown, MO 64133, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

UbiDuo UbiDuo SGD

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	2015-10-27

Official Correspondent

Emma Curry

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

sComm Inc.

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 3008243322. Last updated year: 2026. Please use registration number 3008243322 when referencing this establishment in official correspondence.