Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Reimers and Janssen GmbH · Predicate Candidate Screening
2 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K131080 | PHYSIOLASER OLYMPIC, SINGLE PROBES CW, CLUSTER PROBES CW, LI | Reimers and Janssen GmbH | 2014-06-13 | 445 | 0 |
| K091675 | LASERPEN PRACTISE AND EXPERT, HANDYLASER SPRINT, HANDYLASER | Reimers and Janssen GmbH | 2009-12-15 | 189 | 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