Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3011053282

FEI Number

3011053282

Entity Name

LifeVac, LLC

City/State/Country

Nesconset, NY, US

Establishment Address

110 Lake Ave South, Suite 35, Nesconset, NY 11767, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

LifeVac, LLC (Owner Number: 10047348)

Owner / Operator Contact Address

110 Lake Avenue South, Suite 35, Nesconset, NY 11767, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

DEN250012

PMA Number

N/A

All Registered Proprietary Names

LifeVac

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
QXN	Suction Anti-Choking Device As A Second-Line Treatment	Ear, Nose, Throat	Class 2	874.5400	2026-03-05

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LifeVac, LLC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3011053282. Last updated year: 2026. Please use registration number 3011053282 when referencing this establishment in official correspondence.