# Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG

- Location (FDA's records): Bingen Am Rhein, DE
- FDA decisions: 4 (2015–2020): 4 510(k) clearances
- Names in FDA's records: Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG (3); Argon Med. Productions Vertriebs Gesellschaft Mbh (1)
- Product codes: DZE (3), KCT (1)
- 510(k) review time since 2016: median 371 days, against 223 for FDA's reviews in the same codes and years (0 of 3 faster)
- Predicates its devices cite: 6 (1 its own); citations of its devices by later devices: 1 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Bicon, Inc.: 1 (https://510kreport.com/company/bicon)
- Custom Dental Implants, Inc.: 1 (https://510kreport.com/company/custom-dental-implants)
- Dentsply International, Inc.: 1 (https://510kreport.com/company/dentsply-international)
- Nobel Biocare AB: 1 (https://510kreport.com/company/nobel-biocare)
- Biodenta Swiss AG: 1 (https://510kreport.com/company/biodenta-swiss)

## Its most-cited devices
- K160581: K3PRO Konus Additional Abutments and Implants (2017), cited by 1

## Recent decisions
- K190192: K3Pro Konus New Abutments and Implants (Feb 10, 2020)
- K160581: K3PRO Konus Additional Abutments and Implants (Mar 24, 2017)
- K160574: K3PRO Surgical Tray (Dec 20, 2016)
- K141159: Konus Dental Implant System (Mar 11, 2015)

Source page: https://510kreport.com/company/argon-med-productions-vertriebs-gesellschaft-mbh