Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043364471

FEI Number

3043364471

Entity Name

QuietLab LLC

City/State/Country

New York, NY, US

Establishment Address

447 Broadway Fl 2, New York, NY 10013, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

QuietLab (Owner Number: 10094553)

Owner / Operator Contact Address

Vida Downtown Residences Apt. 46/02, Dubai, AE-DU 00000, AE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K253868

PMA Number

N/A

All Registered Proprietary Names

QuietLab Pro

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LRK	Device, Anti-Snoring	Dental	Class 2	872.5570	2026-01-21

Official Correspondent

Pietro Candriella

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

QuietLab

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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3007108578	TRUE FUNCTION LABORATORY INC	La Mesa, CA, US
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 3043364471. Last updated year: 2026. Please use registration number 3043364471 when referencing this establishment in official correspondence.