Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3043338342

FEI Number

3043338342

Entity Name

GVK CORPORATION

City/State/Country

Reno, NV, US

Establishment Address

5150 Mae Anne Ave, Reno, NV 89523, US

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

GVK Corporation (Owner Number: 10095186)

Owner / Operator Contact Address

5150 Mae Anne Ave, Reno, NV 89523,USA, Reno, NV 89523, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

Antiviral Nasal Spray

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
KCO	Nasal Spray, Ent Delivery	Ear, Nose, Throat	Class 1	874.5220	2026-02-04

Official Correspondent

Liting Li

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

GVK Corporation

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 3043338342. Last updated year: 2026. Please use registration number 3043338342 when referencing this establishment in official correspondence.