SOMNIFIX INTERNATIONAL LLC

FDA Device Registration & Listing · Chevy Chase, MD, US · Registration 3014107776

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3014107776
FEI Number
3014107776
Entity Name
SOMNIFIX INTERNATIONAL LLC
City/State/Country
Chevy Chase, MD, US
Establishment Address
5425 Wisconsin Ave, Suite 600, Chevy Chase, MD 20815, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
SomniFix International LLC (Owner Number: 10056168)
Owner / Operator Contact Address
5425 Wisconsin Ave, Suite 600, Chevy Chase, MD 20815, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SomniFix Sleep Therapy

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LWF Dilator, Nasal Ear, Nose, Throat Class 1 874.3900 2017-11-11

Official Correspondent

Nicholas Michalak

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

SomniFix International LLC
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014107776. Last updated year: 2026. Please use registration number 3014107776 when referencing this establishment in official correspondence.
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