Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3030977779

FEI Number

3030977779

Entity Name

VAYUCLEAR INC

City/State/Country

Charleston, SC, US

Establishment Address

645 Meeting St, Ste 300, Charleston, SC 29403, US

Establishment Type(s)

Develop Specifications But Do Not Manufacture At This Facility

Owner / Operator

Vayuclear Inc (Owner Number: 10090539)

Owner / Operator Contact Address

645 Meeting St., Suite 300, Charleston, SC 29403, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VORTEX

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
BYY	Tube, Aspirating, Flexible, Connecting	General Hospital	Class 2	880.6740	2024-04-10

Official Correspondent

David Maness

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Vayuclear Inc

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 3030977779. Last updated year: 2026. Please use registration number 3030977779 when referencing this establishment in official correspondence.