Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009132214

FEI Number

3009132214

Entity Name

SLEEP JOY INTERNATIONAL LLC

City/State/Country

Northport, NY, US

Establishment Address

140 Main St, Northport, NY 11768, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Sleep Joy International LLC (Owner Number: 10037094)

Owner / Operator Contact Address

140 Main Street, Northport, NY 11768, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K101709

PMA Number

N/A

All Registered Proprietary Names

LambergSleepWell-Smartrusion (LSW-S)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LQZ	Device, Jaw Repositioning	Dental	Class 2	872.5570	2011-06-16
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2011-06-16

Official Correspondent

Steven Lamberg

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sleep Joy International LLC

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

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K122391	Medtronic Xomed, Inc.	MEDTRONIC XOMED, INC.	2013-01-10

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3005726841	BIOTEX, INC.	HOUSTON, TX, US
3030562551	AIOMEGA, LLC	Tyler, TX, US

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009132214. Last updated year: 2026. Please use registration number 3009132214 when referencing this establishment in official correspondence.