Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3008513054

FEI Number

3008513054

Entity Name

KONING CORPORATION

City/State/Country

Norcross, GA, US

Establishment Address

5555 Oakbrook Pkwy Ste 640, Norcross, GA 30093, US

Establishment Type(s)

Complaint File Establishment per 21 CFR 820.198,Manufacture Medical Device

Owner / Operator

Koning Corporation (Owner Number: 10033113)

Owner / Operator Contact Address

5555 Oakbrook Parkway, Suite 640, Norcross, GA 30093, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

P130025

All Registered Proprietary Names

Koning Corporation, Norcross, Georgia

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
OLQ	Cross-Sectional Mammographic Xray System	Unknown	Class 3	N/A	2016-01-22

Official Correspondent

Ty Cowart

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Koning 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 3008513054. Last updated year: 2026. Please use registration number 3008513054 when referencing this establishment in official correspondence.