Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Ritter Implants GmbH & 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) |
|---|---|---|---|---|---|
| K180183 | Ritter Dental Implant System | Ritter Implants GmbH & Co. KG | 2019-01-24 | 366 | 0 |
| K160475 | Ritter Dental Implant System | Ritter Implants GmbH & Co. KG | 2016-12-14 | 299 | 0 |
| K131557 | RITTER IMPLANT SYSTEM | Ritter Implants GmbH CO KG | 2014-05-09 | 345 | 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