THE SNORE RELIEVER COMPANY

FDA Device Registration & Listing · Largo, FL, US · Registration 3008583502

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
3008583502
FEI Number
3008583502
Entity Name
THE SNORE RELIEVER COMPANY
City/State/Country
Largo, FL, US
Establishment Address
8042 118th Ave N, Largo, FL 33773, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
The Snore Reliever Company (Owner Number: 10033460)
Owner / Operator Contact Address
8042 118th Ave, Largo, FL 33773, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K092942
PMA Number
N/A

All Registered Proprietary Names

Vital Sleep Vital Sleep

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRK Device, Anti-Snoring Dental Class 2 872.5570 2025-01-08
LRK Device, Anti-Snoring Dental Class 2 872.5570 2010-08-18

Official Correspondent

David Hernandez

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Snore Reliever Company
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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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008583502. Last updated year: 2026. Please use registration number 3008583502 when referencing this establishment in official correspondence.
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