Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3016784019

FEI Number

3016784019

Entity Name

LIVILITI HEALTH PRODUCTS CORP

City/State/Country

Lake City, FL, US

Establishment Address

2140 SW Main Blvd, Lake City, FL 32025, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Liviliti Health Products Corp (Owner Number: 10071925)

Owner / Operator Contact Address

2140 SW Main Blvd, Lake City, FL 32025, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BYX	Tubing, Pressure And Accessories	Anesthesiology	Class 1	868.5860	2021-06-14

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Liviliti Health Products Corp

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 3016784019. Last updated year: 2026. Please use registration number 3016784019 when referencing this establishment in official correspondence.