Manufacturer registered with FDA
Argon Dental Vertriebs Gmbh & Co. KG
Bingen am Rhein, Germany. Lists 2 dental device types with FDA across 1 registered establishment.
- Device types listed
- 2
- Brands and models
- 4
- 510(k) clearances
- 0as applicant
- Markets registered in
- 21,428 registrations outside the US
- Establishments
- 1Germany
Registered in 2 markets
Where regulators' registries name Argon Dental Vertriebs Gmbh & Co. KG as the manufacturer or the registration holder of a device.
| Market | Regulator | Named as | Name on the registry | Registrations | Issued | Records |
|---|---|---|---|---|---|---|
| United States | FDA | Manufacturer | Argon Dental Vertriebs Gmbh & Co. KG | 2 device types | — | Below |
| European Union | EUDAMED | Manufacturer | Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG | 1,428 | — | Pure Global AI |
Outside the US the count is of all the company's device registrations in that market, dental or not · matched by company name and country · registry data read 12 Nov 2026
Devices listed with FDA
What Argon Dental Vertriebs Gmbh & Co. KG currently lists, by FDA device type, with the brand and model names on the listing.
| Device type | Category | Role | Brands and models | Listed since |
|---|---|---|---|---|
| Root-Form Endosseous ImplantDZE · Class 2 | Dental implants | Maker | K3Pro Konus Additional Abutments and ImplantsK3Pro Konus Dental Implant System | 2015 |
| Endosseous Dental Implant AbutmentNHA · Class 2 | Implant abutments | Maker | K3Pro Konus Additional Abutments and ImplantsK3Pro Konus Dental Implant System | 2015 |
Source: FDA establishment registration & device listing, 510(k) and product classification files · FDA data as of 2 Nov 2026 · snapshot 12 Nov 2026
Also lists devices cleared under other names
Argon Dental Vertriebs Gmbh & Co. KG lists these devices with FDA today. The clearance names a different applicant, as happens after a rename, an acquisition or a private-label agreement.
Original applicants: Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG (3).
| Decided | 510(k) | Device | Applicant | Device type |
|---|---|---|---|---|
| 10 Feb 2020 | K190192 | K3Pro Konus New Abutments and Implants | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG | DZE Root-Form Endosseous Implant |
| 24 Mar 2017 | K160581 | K3PRO Konus Additional Abutments and Implants | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG | DZE Root-Form Endosseous Implant |
| 11 Mar 2015 | K141159 | KONUS DENTAL IMPLANT SYSTEM | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG | DZE Root-Form Endosseous Implant |
Registered establishments
| Establishment | Location | What it does |
|---|---|---|
| ARGON MEDICAL PRODUCTIONS & VERTRIEBS GESELLSCHAFT MBH & CO.FDA reg. 3011575197 | Bingen am Rhein Rhineland-Palatinate, Germany | Manufacturer |
Other names on FDA records
Argon Medical Productions & Vertriebs Gesellschaft mbH & Co. KG
Sources
FDA establishment registration & device listing (search FDA, owner/operator 10048957). FDA 510(k) premarket notification file. FDA data as of 2 Nov 2026; snapshot 12 Nov 2026. The location shown is the address on FDA's record.