Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Sintea Plustek, LLC — 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) |
|---|---|---|---|---|---|
| K140787 | PLS (POSTERIOR LUMBAR SYSTEM) | Sintea Plustek, LLC | 2014-05-30 | 60 | 0 |
| K130402 | SPIDER SYSTEM KOLIBRI CEMENT NEEDLE | Sintea Plustek, LLC | 2013-04-01 | 41 | 0 |
| K112861 | SINTEA PLUSTEK ANTERIOR CERVICAL PLATE SYSTEM | Sintea Plustek, LLC | 2012-02-24 | 147 | 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