Data / Medical devices / Germany / Argon Medical Productions & Vertriebs Gesellschaft MBH & Co.
Argon Medical Productions & Vertriebs Gesellschaft MBH & Co.: FDA-registered device maker in Bingen am Rhein Rhineland-Palatinate, Germany, 4 510(k) clearances
Argon Medical Productions & Vertriebs Gesellschaft MBH & Co. is registered with the FDA (registration 3011575197) in Bingen am Rhein Rhineland-Palatinate, Germany. It lists 3 device types. The FDA files 4 510(k) clearances under its listings, the newest dated February 10, 2020. Registered through 2027. FDA data exported November 3, 2026.
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- FDA registration number
- 3011575197
- Address
- Franz Kirsten Str.1, Bingen am Rhein Rhineland-Palatinate, Germany, D-55411
- Owner or operator
- Argon Dental Vertriebs Gmbh & Co. KG (10048957)
- Roles
- Manufacturer
- First device listed
- March 25, 2015
- Registered through
- 2027
- Brand names listed
- K3Pro Konus Additional Abutments and Implants, K3Pro Konus Dental Implant System, K3Pro Surgical Trays
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Abutment, Implant, Dental, Endosseous | NHA | 2 | Manufacturer | accessdata.fda.gov |
| Implant, Endosseous, Root-Form | DZE | 2 | Manufacturer | accessdata.fda.gov |
| Sterilization Wrap Containers, Trays, Cassettes & Other Accessories | KCT | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 10, 2020 | K190192 | K3Pro Konus New Abutments and Implants | DZE | Substantially Equivalent | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG | accessdata.fda.gov |
| March 24, 2017 | K160581 | K3PRO Konus Additional Abutments and Implants | DZE | Substantially Equivalent | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG | accessdata.fda.gov |
| December 20, 2016 | K160574 | K3PRO SURGICAL TRAY | KCT | Substantially Equivalent | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG | accessdata.fda.gov |
| March 11, 2015 | K141159 | KONUS DENTAL IMPLANT SYSTEM | DZE | Substantially Equivalent | Argon Med. Productions Vertriebs Gesellschaft Mbh | accessdata.fda.gov |
Compare with other makers
- All makers of Abutment, Implant, Dental, Endosseous
- All makers of Implant, Endosseous, Root-Form
- All makers of Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Updated February 10, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.