Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Starmedtec GmbH · 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) |
|---|---|---|---|---|---|
| K121570 | AURIGA QI | Starmedtec GmbH | 2013-01-16 | 232 | 0 |
| K111475 | AURIGA XL | Starmedtec GmbH | 2011-09-28 | 124 | 14 |
| K103654 | VELA XL | Starmedtec GmbH | 2011-04-06 | 112 | 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