Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3010767848

FEI Number

3010767848

Entity Name

Boyd Research

City/State/Country

St Pete Beach, FL, US

Establishment Address

5820 Bali Way S, St Pete Beach, FL 33706, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Boyd Research, Inc. (Owner Number: 10042732)

Owner / Operator Contact Address

5820 Bali Way S, St Pete Beach, FL 33706, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K041184

PMA Number

N/A

All Registered Proprietary Names

SnoreHook

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2015-04-10

Official Correspondent

James Boyd

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Boyd Research, Inc.

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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3006786034	Innovative Health Technologies (NZ) Limited	Dunedin Otago, NZ

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3010767848. Last updated year: 2026. Please use registration number 3010767848 when referencing this establishment in official correspondence.