NEXAIR, LLC.

FDA Device Registration & Listing · Mem, TN, US · Registration 1020303

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1020303
FEI Number
1020303
Entity Name
NEXAIR, LLC.
City/State/Country
Mem, TN, US
Establishment Address
1211 NORTH MCLEAN BLVD., Mem, TN 38108, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
NEXAIR, LLC (Owner Number: 9020571)
Owner / Operator Contact Address
1350 Concourse Avenue, Suite 103, Memphis, TN 38104, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Laser Gas Mixture Calibration Gas Mixture, Lung Diffusion Test Mixture, Clinical Blood Gas Mixture

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 2007-12-17
BXK Gas, Calibration (Specified Concentration) Anesthesiology Class 1 868.6400 1995-05-30

Official Correspondent

JP Deaton

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

NEXAIR, 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
1054077 NEXAIR, LLC FAIRBURN, GA, US

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1020303. Last updated year: 2026. Please use registration number 1020303 when referencing this establishment in official correspondence.
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