G & G PRODUCTS, LLC

FDA Device Registration & Listing · Kennebunk, ME, US · Registration 3011956575

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
3011956575
FEI Number
3011956575
Entity Name
G & G PRODUCTS, LLC
City/State/Country
Kennebunk, ME, US
Establishment Address
70 Twine Mill Rd, Kennebunk, ME 04043, US
Establishment Type(s)
Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device,Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
G & G Products, LLC (Owner Number: 10092387)
Owner / Operator Contact Address
70 Twine Mill Road, Kennebunk, ME 04043, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Snore Buds

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 2025-12-31

Official Correspondent

Gary Gagnon

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

G & G Products, 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 3011956575. Last updated year: 2026. Please use registration number 3011956575 when referencing this establishment in official correspondence.
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