Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011776382

FEI Number

3011776382

Entity Name

MOONLIGHT SLUMBER, INC.

City/State/Country

Elgin, IL, US

Establishment Address

60 Ann St, Elgin, IL 60120, US

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer)

Owner / Operator

Moonlight Slumber, LLC (Owner Number: 10049675)

Owner / Operator Contact Address

60 Ann Street, Elgin, IL 60120, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Medline pads

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LWG	Surgical Table Cushion	General, Plastic Surgery	Class 1	878.4950	2022-05-23
IKY	Mattress, Flotation Therapy, Non-Powered	General Hospital	Class 1	880.5150	2015-07-08

Official Correspondent

Robert Apitz

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Moonlight Slumber, 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 3011776382. Last updated year: 2026. Please use registration number 3011776382 when referencing this establishment in official correspondence.