Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3042888274

FEI Number

3042888274

Entity Name

VITAL AIR FZCO

City/State/Country

Dubai Dubayy, AE

Establishment Address

FC0400WS137, Al Wafa Food Court, JAFZA, Dubai Dubayy 262492, AE

Establishment Type(s)

Export Device to the United States But Perform No Other Operation on Device

Owner / Operator

VITAL AIR FZCO (Owner Number: 10094840)

Owner / Operator Contact Address

FC0400WS137, Al Wafa Food Court, JAFZA, Dubai, AE-DU 262492, AE

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

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
CCW	Laryngoscope, Rigid	Anesthesiology	Class 1	868.5540	2025-12-29
HLJ	Ophthalmoscope, Battery-Powered	Ophthalmic	Class 2	886.1570	2025-12-29
ERA	Otoscope	Ear, Nose, Throat	Class 1	874.4770	2025-12-29

Official Correspondent

No official correspondent registered.

US Agent Details

Alan Schwartz Business: mdi Consultants Inc Email: info@mdiconsultants.com Phone: (516) 4829001

Related Public Records

Same Entity

VITAL AIR FZCO

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
K932506	Rudolf Riester GmbH & Co. KG	RI-SCOPE (S)	1993-10-08

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0144-2024	Covidien	1	Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000
Z-0168-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-017-000, Sterile EO, Rx Only
Z-0169-2024	Covidien	1	McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3042888274. Last updated year: 2026. Please use registration number 3042888274 when referencing this establishment in official correspondence.