K3Pro Konus Dental Implants (UDI VBA_LK01)
Manufactured by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG
Device Regulatory Overview
The K3Pro Konus Dental Implants (Model/Catalog Number: VBA_LK01) 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
- VBA_LK01
- Product Code / EMDN
- NDP
- Device Name
- RapidFix Locator/ Finder Cap
- Database Sync Date
- 2026-08-09 09:23:54
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)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 VBA_LK01.
What classification code is assigned to this device?
This device is registered under product classification code NDP.
Similar Classification Devices (NDP)
Other Devices by Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG
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