GUDIDData
gudid Primary ID: VSK3K

K3Pro Konus Dental Implants (UDI VSK3K)

Manufactured by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for K3Pro Konus Dental Implants - Primary ID VSK3K

Device Regulatory Overview

The K3Pro Konus Dental Implants (Model/Catalog Number: VSK3K) is a medical device manufactured by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG. This product is indexed under FDA Product Code / Category Classification NDP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VSK3K
Product Code / EMDN
NDP
Device Name
Healing/ Sealing Screw for K3Pro w/ 3mm Well
Database Sync Date
2026-08-09 09:23:54

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of K3Pro Konus Dental Implants?

The registered manufacturer of record for K3Pro Konus Dental Implants is Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG.

What is the Primary UDI-DI identifier for K3Pro Konus Dental Implants?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VSK3K.

What classification code is assigned to this device?

This device is registered under product classification code NDP.

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