Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009522781

FEI Number

3009522781

Entity Name

Airocide Systems

City/State/Country

Neptune Beach, FL, US

Establishment Address

2300 Marshpoint Road, Suite 202, Neptune Beach, FL 32266, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Airocide Systems (Owner Number: 10094867)

Owner / Operator Contact Address

2300 Marsh Point Road, Suite 202, Neptune Beach, FL 32266, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K052732

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
FRA	Purifier, Air, Ultraviolet, Medical	General Hospital	Class 2	880.6500	2025-12-30

Official Correspondent

Jeff Brown

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Airocide Systems

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 3009522781. Last updated year: 2026. Please use registration number 3009522781 when referencing this establishment in official correspondence.