Predicate Research Report · generated 2026-08-22 · Print / save as PDF · Save to account
Besteam Technology, Inc. · Predicate Candidate Screening
4 FDA 510(k) clearances under this manufacturer; the 50 most recent screened below.
| K-number | Device | Applicant | Decided | Review days | Recalls (K-match) |
|---|---|---|---|---|---|
| K083303 | LANDLEX, MODEL: 402X | Besteam Technology, Inc. | 2009-01-26 | 77 | 0 |
| K081980 | KYMCO FORU, MODEL EQ35 | Besteam Technology, Inc. | 2008-08-04 | 24 | 0 |
| K063196 | LANDLEX, MODEL S403X | Besteam Technology, Inc. | 2007-01-23 | 95 | 0 |
| K060042 | LANDLEX, MODEL P100X | Besteam Technology, Inc. | 2006-02-14 | 39 | 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