Not currently registered with FDA under this name
Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG
Bingen Am Rhein, Germany. Named as applicant on 3 dental 510(k) clearances between 2015 and 2020. No establishment is registered with FDA under this exact name today.
- Device types listed
- 0
- Brands and models
- 0
- 510(k) clearances
- 32015–2020
- Markets registered in
- 1United States
- Establishments
- 0—
510(k) clearances per year, 2007–2026
510(k) clearances
Clearances on which FDA names Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG as the applicant.
| Decided | 510(k) | Device | Device type |
|---|---|---|---|
| 10 Feb 2020 | K190192 | K3Pro Konus New Abutments and Implants | DZE Root-Form Endosseous Implant |
| 24 Mar 2017 | K160581 | K3PRO Konus Additional Abutments and Implants | DZE Root-Form Endosseous Implant |
| 11 Mar 2015 | K141159 | KONUS DENTAL IMPLANT SYSTEM | DZE Root-Form Endosseous Implant |
Some of these clearances are listed with FDA today by another company: Argon Dental Vertriebs Gmbh & Co. KG (3).
Sources
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 of the most recent filing, which can be a US agent.