Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009227226

FEI Number

3009227226

Entity Name

AIRMAX B.V.

City/State/Country

Oegstgeest Zuid-Holland, NL

Establishment Address

Rhijngeesterstraatweg 58-B, Oegstgeest Zuid-Holland 2341BV, NL

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Airmax B.V. (Owner Number: 10036296)

Owner / Operator Contact Address

Rhijngeesterstraatweg 58-B, Oegstgeest, NL-ZH 2341 BV, NL

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Airmax

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LWF	Dilator, Nasal	Ear, Nose, Throat	Class 1	874.3900	2011-04-28

Official Correspondent

No official correspondent registered.

US Agent Details

Devin Benner Business: McKeon Products Email: tamara@macksearplugs.com Phone: (586) 4277560

Related Public Records

Same Entity

Airmax B.V.

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 3009227226. Last updated year: 2026. Please use registration number 3009227226 when referencing this establishment in official correspondence.