Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3006794225

FEI Number

3006794225

Entity Name

Sleep Science Partners, Inc.

City/State/Country

Larkspur, CA, US

Establishment Address

700 Larkspur Landing Circle, Suite 245, Larkspur, CA 94939, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Sleep Science Partners, Inc. (Owner Number: 10023348)

Owner / Operator Contact Address

700 Larkspur Landing Circle, Suite 245, Larkspur, CA 94939, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K190058

PMA Number

N/A

All Registered Proprietary Names

PureSleep (OTC)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2019-07-23

Official Correspondent

Noel Lindsay

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Sleep Science Partners, 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 3006794225. Last updated year: 2026. Please use registration number 3006794225 when referencing this establishment in official correspondence.