Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Xiamen Double Engine Medical Material Co., Ltd. — 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) |
|---|---|---|---|---|---|
| K131609 | DOUBLE ENGINE INTRAMEDDULLARY NAIL SYSTEM | Xiamen Double Engine Medical Material Co., Ltd. | 2014-05-21 | 352 | 0 |
| K130108 | DOUBLE ENGINE BONE PLATE AND SCREW SYSTEMS | Xiamen Double Engine Medical Material Co., Ltd. | 2013-04-19 | 93 | 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