AIRIVER MEDICAL

FDA Device Registration & Listing · Brooklyn Park, MN, US · Registration 3031531314

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
3031531314
FEI Number
3031531314
Entity Name
AIRIVER MEDICAL
City/State/Country
Brooklyn Park, MN, US
Establishment Address
7601 Northland Dr N Ste 170, Brooklyn Park, MN 55428, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Airiver Medical (Owner Number: 10095448)
Owner / Operator Contact Address
7601 Northland Dr N, Suite 170, Brooklyn Park, MN 55428, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

FESStus Sinus Seeker

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LRC Instrument, Ent Manual Surgical Ear, Nose, Throat Class 1 874.4420 2026-03-13

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Airiver Medical
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K143738 Intuit Medical Products, LLC DSS Sinusplasty Balloon Catheter 2015-08-27

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3031531314. Last updated year: 2026. Please use registration number 3031531314 when referencing this establishment in official correspondence.
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