Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

1620065

FEI Number

1620065

Entity Name

AIRGAS USA, LLC

City/State/Country

Grand Prairie, TX, US

Establishment Address

801 W Carrier Pkwy, Grand Prairie, TX 75050, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

AIRGAS USA, LLC (Owner Number: 9008516)

Owner / Operator Contact Address

31 North Peoria Avenue, --, Tulsa, OK 74120, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Laser Gas Pulmonary Function Mixture Biological Atmosphere (Aerobic) Monitor Mixture Blood Gas Biological Atmosphere (Anaerobic) Calibration Gas Mixtures Lung Diffusion Gas Laser Gas

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NXF	Gas, Laser Generating	General, Plastic Surgery	Class 1	878.4810	2007-12-04
BXK	Gas, Calibration (Specified Concentration)	Anesthesiology	Class 1	868.6400	1992-07-09

Official Correspondent

Brandon Ketcher

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

AIRGAS USA, LLC

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

View Entity Profile →

Other Registrations for Same Entity

Registration Number	Establishment Name	Location
3007313217	Airgas USA, LLC.	La Porte, TX, US
1645341	AIRGAS USA, LLC	TULSA, OK, US
3004931173	AIRGAS USA LLC	Elk Grove Village, IL, US
1033831	AIRGAS USA, LLC.	ATL, GA, US
2127612	AIRGAS USA LLC	Waukesha, WI, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1620065. Last updated year: 2026. Please use registration number 1620065 when referencing this establishment in official correspondence.