Predicate Research Report · generated 2026-08-23 · Print / save as PDF · Save to account
Twin Star Medical, Inc. · 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) |
|---|---|---|---|---|---|
| K131966 | TWIN STAR EXTREMITY COMPARTMENT SYNDROME MONITOR AND FLUID C | Twin Star Medical, Inc. | 2014-02-07 | 224 | 0 |
| K090961 | TWIN STAR COMPARTMENT PRESSURE MONITOR AND FLUID COLLECTION | Twin Star Medical, Inc. | 2009-06-12 | 67 | 0 |
| K041771 | TWIN STAR COMPARTMENT SYNDROME PRESSURE MONITORING AND FLUID | Twin Star Medical, Inc. | 2004-09-14 | 76 | 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