Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Rhythm Xience, Inc. (Rxi) · 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) |
|---|---|---|---|---|---|
| K171081 | Guider Catheter Introducer | Rhythm Xience, Inc. (Rxi) | 2017-05-09 | 28 | 0 |
| K170373 | Flextra Steerable Introducer | Rhythm Xience, Inc. (Rxi) | 2017-02-27 | 20 | 4 |
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