Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG · Predicate Candidate Screening
3 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K190192 | K3Pro Konus New Abutments and Implants | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG | 2020-02-10 | 371 | 0 |
| K160581 | K3PRO Konus Additional Abutments and Implants | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG | 2017-03-24 | 388 | 0 |
| K160574 | K3PRO SURGICAL TRAY | Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG | 2016-12-20 | 294 | 0 |
Methodology
Recall counts reflect FDA recall records explicitly referencing each K-number; FDA links recalls to K-numbers inconsistently, so 0 means "none found in FDA records," not "never recalled." Data: FDA openFDA, refreshed weekly. Verify decisions of consequence against the primary source. Full candidate set and CSV export: atlasbyauro.com.
Prepared with Atlas
Predicate research, review-time statistics and recall monitoring for 510(k) teams: atlasbyauro.com/fda